Showing NP-Card for Roseoferin B2 (NP0003265)
| Record Information | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Version | 2.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Created at | 2020-12-09 00:32:31 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Updated at | 2021-07-15 16:45:57 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| NP-MRD ID | NP0003265 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Common Name | Roseoferin B2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Provided By | NPAtlas | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | Roseoferin B2 is found in Mycogone rosea. Based on a literature review very few articles have been published on 6-hydroxy-2-({hydroxy[1-(2-methyldecanoyl)pyrrolidin-2-yl]methylidene}amino)-N-{1-[(1-{[1-({1-[(1-{[1-({1-[(2-hydroxyethyl)amino]propan-2-yl}-C-hydroxycarbonimidoyl)-1-methylethyl]-C-hydroxycarbonimidoyl}-1-methylethyl)-C-hydroxycarbonimidoyl]-2-methylpropyl}-C-hydroxycarbonimidoyl)-2-methylbutyl]-C-hydroxycarbonimidoyl}-1-methylethyl)-C-hydroxycarbonimidoyl]ethyl}-4-methyl-8-oxodecanimidic acid. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structure |  MOL for NP0003265 (Roseoferin B2)
Mrv1652307012117073D
186186 0 0 0 0 999 V2000
-14.4159 5.8769 0.9783 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.0110 5.2324 -0.3022 C 0 0 2 0 0 0 0 0 0 0 0 0
-14.6540 3.8490 -0.5206 C 0 0 1 0 0 0 0 0 0 0 0 0
-14.3571 2.9575 0.6359 C 0 0 1 0 0 0 0 0 0 0 0 0
-14.7353 1.5394 0.5293 C 0 0 2 0 0 0 0 0 0 0 0 0
-13.7402 0.6149 1.3136 C 0 0 2 0 0 0 0 0 0 0 0 0
-12.5184 0.5625 0.3893 C 0 0 1 0 0 0 0 0 0 0 0 0
-11.8963 1.8689 0.2027 C 0 0 1 0 0 0 0 0 0 0 0 0
-11.0832 1.9148 -1.0880 C 0 0 1 0 0 0 0 0 0 0 0 0
-10.7442 3.4728 -1.3027 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.9752 1.1213 -1.2056 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.2986 1.4221 0.2103 O 0 0 0 0 0 0 0 0 0 0 0 0
-9.0752 0.2930 -1.6555 N 0 0 0 0 0 0 0 0 0 0 0 0
-9.6486 -0.5211 -2.8765 C 0 0 1 0 0 0 0 0 0 0 0 0
-8.5254 -0.5277 -3.8350 C 0 0 2 0 0 0 0 0 0 0 0 0
-7.3947 0.2153 -3.1689 C 0 0 2 0 0 0 0 0 0 0 0 0
-7.8159 -0.1674 -1.6192 C 0 0 1 0 0 0 0 0 0 0 0 0
-6.6075 0.0435 -0.9004 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.6536 0.7268 -1.3877 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.4633 -0.5541 0.3880 N 0 0 0 0 0 0 0 0 0 0 0 0
-5.2129 -0.6106 0.9776 C 0 0 2 0 0 0 0 0 0 0 0 0
-5.1326 -1.7551 1.9824 C 0 0 2 0 0 0 0 0 0 0 0 0
-5.7247 -3.0127 1.2898 C 0 0 1 0 0 0 0 0 0 0 0 0
-4.8768 -3.4630 0.1388 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.0758 -4.0495 2.2951 C 0 0 2 0 0 0 0 0 0 0 0 0
-7.2223 -4.8791 1.8266 C 0 0 1 0 0 0 0 0 0 0 0 0
-8.2944 -3.8597 1.7815 O 0 0 0 0 0 0 0 0 0 0 0 0
-7.2369 -5.3819 0.4217 C 0 0 1 0 0 0 0 0 0 0 0 0
-8.5734 -6.1173 0.2690 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.4261 -6.0015 1.0323 O 0 0 0 0 0 0 0 0 0 0 0 0
-8.6977 -6.9642 -0.9861 C 0 0 1 0 0 0 0 0 0 0 0 0
-7.6061 -8.0249 -0.8318 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.1766 0.3053 0.8591 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.7015 0.4758 -0.4412 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.5740 1.0632 1.8047 N 0 0 0 0 0 0 0 0 0 0 0 0
-2.3023 1.7577 1.3230 C 0 0 1 0 0 0 0 0 0 0 0 0
-1.7691 2.2877 2.5967 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6109 0.3986 0.9351 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6705 -0.4395 1.9599 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.0705 0.1161 -0.2189 N 0 0 0 0 0 0 0 0 0 0 0 0
-0.4564 -0.9862 -0.8945 C 0 0 1 0 0 0 0 0 0 0 0 0
-1.2142 -2.2573 -0.9445 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0428 -0.5381 -2.2179 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8125 -1.2758 0.0516 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4709 -1.4725 1.2404 O 0 0 0 0 0 0 0 0 0 0 0 0
1.9957 -1.1866 -0.5716 N 0 0 0 0 0 0 0 0 0 0 0 0
3.2957 -1.1579 -0.4237 C 0 0 2 0 0 0 0 0 0 0 0 0
4.6572 -1.1768 -0.1698 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6087 -1.3782 0.3937 O 0 0 0 0 0 0 0 0 0 0 0 0
5.2291 -0.3941 -1.5821 N 0 0 0 0 0 0 0 0 0 0 0 0
6.4682 0.2010 -1.3264 C 0 0 1 0 0 0 0 0 0 0 0 0
7.6421 0.7638 -1.0718 C 0 0 0 0 0 0 0 0 0 0 0 0
8.3080 1.6489 -1.5993 O 0 0 0 0 0 0 0 0 0 0 0 0
8.4684 0.2098 0.2153 N 0 0 0 0 0 0 0 0 0 0 0 0
9.4138 1.2302 0.5559 C 0 0 1 0 0 0 0 0 0 0 0 0
9.0705 2.6564 0.3057 C 0 0 0 0 0 0 0 0 0 0 0 0
9.2054 1.2525 2.1995 C 0 0 0 0 0 0 0 0 0 0 0 0
10.7602 0.7473 0.3875 C 0 0 0 0 0 0 0 0 0 0 0 0
11.5926 0.6658 1.3111 O 0 0 0 0 0 0 0 0 0 0 0 0
11.2512 0.3212 -0.9204 N 0 0 0 0 0 0 0 0 0 0 0 0
12.5218 0.0167 -1.1601 C 0 0 1 0 0 0 0 0 0 0 0 0
12.4024 -0.6872 -2.6681 C 0 0 0 0 0 0 0 0 0 0 0 0
13.2404 1.2842 -1.6053 C 0 0 0 0 0 0 0 0 0 0 0 0
13.4943 -0.9823 -0.6371 C 0 0 0 0 0 0 0 0 0 0 0 0
13.2243 -2.1688 -0.5167 O 0 0 0 0 0 0 0 0 0 0 0 0
14.7915 -0.4670 -0.3190 N 0 0 0 0 0 0 0 0 0 0 0 0
16.0920 -0.6508 -0.0112 C 0 0 2 0 0 0 0 0 0 0 0 0
16.4064 -2.0331 0.6108 C 0 0 0 0 0 0 0 0 0 0 0 0
16.5247 0.2959 1.1576 C 0 0 2 0 0 0 0 0 0 0 0 0
16.0559 1.5916 0.9634 N 0 0 0 0 0 0 0 0 0 0 0 0
16.2642 2.5577 0.0795 C 0 0 2 0 0 0 0 0 0 0 0 0
17.4531 3.4231 -0.0601 C 0 0 1 0 0 0 0 0 0 0 0 0
18.6599 2.8377 -0.3250 O 0 0 0 0 0 0 0 0 0 0 0 0
5.7396 1.6244 -1.9511 C 0 0 2 0 0 0 0 0 0 0 0 0
6.6059 2.6862 -2.3700 C 0 0 0 0 0 0 0 0 0 0 0 0
5.0314 2.1723 -0.7030 C 0 0 0 0 0 0 0 0 0 0 0 0
3.0696 -1.1077 1.4174 C 0 0 2 0 0 0 0 0 0 0 0 0
2.4648 0.1840 1.6317 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3039 -1.5192 2.0205 C 0 0 1 0 0 0 0 0 0 0 0 0
4.1720 -1.5479 3.5866 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.2592 5.4436 1.4979 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.5315 6.9578 0.8868 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.4831 5.7780 1.6519 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.9234 5.1385 -0.3941 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.3559 5.8814 -1.1558 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.7012 3.9156 -0.7987 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.1497 3.3676 -1.4152 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.6670 3.2777 1.4035 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.3634 3.3152 1.3591 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.6247 1.2111 -0.5680 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.7446 1.2439 0.7928 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.1245 -0.3848 1.3912 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.5506 1.0806 2.2565 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.8589 -0.2581 0.7180 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.9107 0.1761 -0.6128 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.1626 2.8283 0.4781 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.9555 1.7355 1.0537 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.8683 1.7603 -1.9009 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7515 3.8281 -1.6880 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.9781 3.4836 -2.0563 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.4763 3.8162 -0.3146 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.7157 -1.5070 -2.3820 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.5307 -0.0468 -3.1843 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.7713 -0.1273 -4.8123 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.1091 -1.5876 -3.9809 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.5312 1.3036 -3.1308 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.3885 -0.1654 -3.2431 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.8960 -1.3329 -1.7680 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.3627 -0.8307 0.8806 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.7302 -1.4119 0.0221 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.4986 -1.6125 2.9750 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.9896 -2.0049 2.0533 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.6615 -2.6561 0.8507 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.7486 -4.5762 0.2655 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.2593 -3.2738 -0.8567 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7902 -3.0885 0.1824 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.2561 -3.6723 3.3188 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.1817 -4.7200 2.3970 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.4738 -5.6443 2.5461 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.7553 -3.9148 2.6317 H 0 0 0 0 0 0 0 0 0 0 0 0
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-9.6898 -7.4085 -1.0133 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.5466 -6.2972 -1.8153 H 0 0 0 0 0 0 0 0 0 0 0 0
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-3.9058 1.2479 2.7522 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.4008 2.2837 0.4731 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.8076 2.7586 2.6225 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.7724 1.4397 3.3909 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.5404 3.0429 2.9558 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.0563 1.0342 -0.9320 H 0 0 0 0 0 0 0 0 0 0 0 0
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-1.3457 -2.7134 0.0312 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3721 -1.3771 -2.8716 H 0 0 0 0 0 0 0 0 0 0 0 0
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-0.8155 0.0082 -2.7603 H 0 0 0 0 0 0 0 0 0 0 0 0
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3.2110 0.1870 -0.2296 H 0 0 0 0 0 0 0 0 0 0 0 0
4.5907 -0.5555 -2.2342 H 0 0 0 0 0 0 0 0 0 0 0 0
6.0356 0.4287 -0.1028 H 0 0 0 0 0 0 0 0 0 0 0 0
8.1541 -0.6597 0.4715 H 0 0 0 0 0 0 0 0 0 0 0 0
8.5728 2.8593 -0.6039 H 0 0 0 0 0 0 0 0 0 0 0 0
10.0124 3.3199 0.3425 H 0 0 0 0 0 0 0 0 0 0 0 0
8.3815 3.0923 1.1172 H 0 0 0 0 0 0 0 0 0 0 0 0
8.1620 1.5477 2.2922 H 0 0 0 0 0 0 0 0 0 0 0 0
9.4975 0.2537 2.4641 H 0 0 0 0 0 0 0 0 0 0 0 0
9.8356 2.0786 2.4753 H 0 0 0 0 0 0 0 0 0 0 0 0
10.4885 0.2187 -1.6926 H 0 0 0 0 0 0 0 0 0 0 0 0
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14.0785 1.5856 -1.0902 H 0 0 0 0 0 0 0 0 0 0 0 0
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13.4141 1.3176 -2.6827 H 0 0 0 0 0 0 0 0 0 0 0 0
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16.8046 -0.5822 -0.8280 H 0 0 0 0 0 0 0 0 0 0 0 0
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17.6782 0.3460 1.0083 H 0 0 0 0 0 0 0 0 0 0 0 0
16.2752 -0.1561 2.0910 H 0 0 0 0 0 0 0 0 0 0 0 0
15.1594 1.7594 1.5803 H 0 0 0 0 0 0 0 0 0 0 0 0
15.3673 3.2689 0.0649 H 0 0 0 0 0 0 0 0 0 0 0 0
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17.1986 4.1124 -0.9516 H 0 0 0 0 0 0 0 0 0 0 0 0
17.5736 4.1636 0.7994 H 0 0 0 0 0 0 0 0 0 0 0 0
19.2876 3.5767 -0.6452 H 0 0 0 0 0 0 0 0 0 0 0 0
5.0017 1.3015 -2.6537 H 0 0 0 0 0 0 0 0 0 0 0 0
7.4380 2.4634 -3.1062 H 0 0 0 0 0 0 0 0 0 0 0 0
5.8647 3.3063 -3.1164 H 0 0 0 0 0 0 0 0 0 0 0 0
6.8777 3.5065 -1.6923 H 0 0 0 0 0 0 0 0 0 0 0 0
4.1132 2.6868 -0.9295 H 0 0 0 0 0 0 0 0 0 0 0 0
4.9302 1.4361 0.0614 H 0 0 0 0 0 0 0 0 0 0 0 0
5.7724 2.9417 -0.2228 H 0 0 0 0 0 0 0 0 0 0 0 0
2.3968 -1.9782 1.3399 H 0 0 0 0 0 0 0 0 0 0 0 0
1.8240 0.2952 2.5074 H 0 0 0 0 0 0 0 0 0 0 0 0
3.3113 0.9440 1.9171 H 0 0 0 0 0 0 0 0 0 0 0 0
1.9793 0.7062 0.7524 H 0 0 0 0 0 0 0 0 0 0 0 0
4.6509 -2.6036 1.8479 H 0 0 0 0 0 0 0 0 0 0 0 0
5.1624 -0.7786 1.9407 H 0 0 0 0 0 0 0 0 0 0 0 0
5.2294 -1.5091 3.9125 H 0 0 0 0 0 0 0 0 0 0 0 0
3.7669 -2.5221 3.8875 H 0 0 0 0 0 0 0 0 0 0 0 0
3.6317 -0.6584 3.8906 H 0 0 0 0 0 0 0 0 0 0 0 0
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2 3 1 0 0 0 0
3 4 1 0 0 0 0
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17 13 1 0 0 0 0
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6 92 1 0 0 0 0
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7 94 1 0 0 0 0
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8 97 1 0 0 0 0
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10 99 1 0 0 0 0
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14102 1 0 0 0 0
14103 1 0 0 0 0
15104 1 0 0 0 0
15105 1 0 0 0 0
16106 1 0 0 0 0
16107 1 0 0 0 0
17108 1 6 0 0 0
20109 1 0 0 0 0
21110 1 6 0 0 0
22111 1 0 0 0 0
22112 1 0 0 0 0
23113 1 6 0 0 0
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80184 1 0 0 0 0
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80186 1 0 0 0 0
M END
3D MOL for NP0003265 (Roseoferin B2)
RDKit 3D
186186 0 0 0 0 0 0 0 0999 V2000
-14.4159 5.8769 0.9783 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.0110 5.2324 -0.3022 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.6540 3.8490 -0.5206 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.3571 2.9575 0.6359 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.7353 1.5394 0.5293 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.7402 0.6149 1.3136 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.5184 0.5625 0.3893 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.8963 1.8689 0.2027 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.0832 1.9148 -1.0880 C 0 0 1 0 0 0 0 0 0 0 0 0
-10.7442 3.4728 -1.3027 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.9752 1.1213 -1.2056 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.2986 1.4221 0.2103 O 0 0 0 0 0 0 0 0 0 0 0 0
-9.0752 0.2930 -1.6555 N 0 0 0 0 0 0 0 0 0 0 0 0
-9.6486 -0.5211 -2.8765 C 0 0 0 0 0 0 0 0 0 0 0 0
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80184 1 0
80185 1 0
80186 1 0
M END
3D SDF for NP0003265 (Roseoferin B2)
Mrv1652307012117073D
186186 0 0 0 0 999 V2000
-14.4159 5.8769 0.9783 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.0110 5.2324 -0.3022 C 0 0 2 0 0 0 0 0 0 0 0 0
-14.6540 3.8490 -0.5206 C 0 0 1 0 0 0 0 0 0 0 0 0
-14.3571 2.9575 0.6359 C 0 0 1 0 0 0 0 0 0 0 0 0
-14.7353 1.5394 0.5293 C 0 0 2 0 0 0 0 0 0 0 0 0
-13.7402 0.6149 1.3136 C 0 0 2 0 0 0 0 0 0 0 0 0
-12.5184 0.5625 0.3893 C 0 0 1 0 0 0 0 0 0 0 0 0
-11.8963 1.8689 0.2027 C 0 0 1 0 0 0 0 0 0 0 0 0
-11.0832 1.9148 -1.0880 C 0 0 1 0 0 0 0 0 0 0 0 0
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-8.5254 -0.5277 -3.8350 C 0 0 2 0 0 0 0 0 0 0 0 0
-7.3947 0.2153 -3.1689 C 0 0 2 0 0 0 0 0 0 0 0 0
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0.8125 -1.2758 0.0516 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4709 -1.4725 1.2404 O 0 0 0 0 0 0 0 0 0 0 0 0
1.9957 -1.1866 -0.5716 N 0 0 0 0 0 0 0 0 0 0 0 0
3.2957 -1.1579 -0.4237 C 0 0 2 0 0 0 0 0 0 0 0 0
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6.4682 0.2010 -1.3264 C 0 0 1 0 0 0 0 0 0 0 0 0
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8.3080 1.6489 -1.5993 O 0 0 0 0 0 0 0 0 0 0 0 0
8.4684 0.2098 0.2153 N 0 0 0 0 0 0 0 0 0 0 0 0
9.4138 1.2302 0.5559 C 0 0 1 0 0 0 0 0 0 0 0 0
9.0705 2.6564 0.3057 C 0 0 0 0 0 0 0 0 0 0 0 0
9.2054 1.2525 2.1995 C 0 0 0 0 0 0 0 0 0 0 0 0
10.7602 0.7473 0.3875 C 0 0 0 0 0 0 0 0 0 0 0 0
11.5926 0.6658 1.3111 O 0 0 0 0 0 0 0 0 0 0 0 0
11.2512 0.3212 -0.9204 N 0 0 0 0 0 0 0 0 0 0 0 0
12.5218 0.0167 -1.1601 C 0 0 1 0 0 0 0 0 0 0 0 0
12.4024 -0.6872 -2.6681 C 0 0 0 0 0 0 0 0 0 0 0 0
13.2404 1.2842 -1.6053 C 0 0 0 0 0 0 0 0 0 0 0 0
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13.2243 -2.1688 -0.5167 O 0 0 0 0 0 0 0 0 0 0 0 0
14.7915 -0.4670 -0.3190 N 0 0 0 0 0 0 0 0 0 0 0 0
16.0920 -0.6508 -0.0112 C 0 0 2 0 0 0 0 0 0 0 0 0
16.4064 -2.0331 0.6108 C 0 0 0 0 0 0 0 0 0 0 0 0
16.5247 0.2959 1.1576 C 0 0 2 0 0 0 0 0 0 0 0 0
16.0559 1.5916 0.9634 N 0 0 0 0 0 0 0 0 0 0 0 0
16.2642 2.5577 0.0795 C 0 0 2 0 0 0 0 0 0 0 0 0
17.4531 3.4231 -0.0601 C 0 0 1 0 0 0 0 0 0 0 0 0
18.6599 2.8377 -0.3250 O 0 0 0 0 0 0 0 0 0 0 0 0
5.7396 1.6244 -1.9511 C 0 0 2 0 0 0 0 0 0 0 0 0
6.6059 2.6862 -2.3700 C 0 0 0 0 0 0 0 0 0 0 0 0
5.0314 2.1723 -0.7030 C 0 0 0 0 0 0 0 0 0 0 0 0
3.0696 -1.1077 1.4174 C 0 0 2 0 0 0 0 0 0 0 0 0
2.4648 0.1840 1.6317 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3039 -1.5192 2.0205 C 0 0 1 0 0 0 0 0 0 0 0 0
4.1720 -1.5479 3.5866 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.2592 5.4436 1.4979 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.5315 6.9578 0.8868 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.4831 5.7780 1.6519 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.9234 5.1385 -0.3941 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.3559 5.8814 -1.1558 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.7012 3.9156 -0.7987 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.1497 3.3676 -1.4152 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.6670 3.2777 1.4035 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.3634 3.3152 1.3591 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.6247 1.2111 -0.5680 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.7446 1.2439 0.7928 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.1245 -0.3848 1.3912 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.5506 1.0806 2.2565 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.8589 -0.2581 0.7180 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.9107 0.1761 -0.6128 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.1626 2.8283 0.4781 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.9555 1.7355 1.0537 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.8683 1.7603 -1.9009 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.7515 3.8281 -1.6880 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.9781 3.4836 -2.0563 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.4763 3.8162 -0.3146 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.7157 -1.5070 -2.3820 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.5307 -0.0468 -3.1843 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.7713 -0.1273 -4.8123 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.1091 -1.5876 -3.9809 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.5312 1.3036 -3.1308 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.3885 -0.1654 -3.2431 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.8960 -1.3329 -1.7680 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.3627 -0.8307 0.8806 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.7302 -1.4119 0.0221 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.4986 -1.6125 2.9750 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.9896 -2.0049 2.0533 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.6615 -2.6561 0.8507 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.7486 -4.5762 0.2655 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.2593 -3.2738 -0.8567 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7902 -3.0885 0.1824 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.2561 -3.6723 3.3188 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.1817 -4.7200 2.3970 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.4738 -5.6443 2.5461 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.7553 -3.9148 2.6317 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.3052 -4.5386 -0.3113 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.4953 -6.0547 0.0940 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.6898 -7.4085 -1.0133 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.5466 -6.2972 -1.8153 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.3819 -8.1586 0.2338 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.6804 -7.6169 -1.3560 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.9627 -8.9073 -1.3291 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.9058 1.2479 2.7522 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.4008 2.2837 0.4731 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.8076 2.7586 2.6225 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.7724 1.4397 3.3909 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.5404 3.0429 2.9558 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.0563 1.0342 -0.9320 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.1252 -2.0717 -1.4647 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.5770 -2.9633 -1.5361 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.3457 -2.7134 0.0312 H 0 0 0 0 0 0 0 0 0 0 0 0
0.3721 -1.3771 -2.8716 H 0 0 0 0 0 0 0 0 0 0 0 0
0.7906 0.2967 -2.1148 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.8155 0.0082 -2.7603 H 0 0 0 0 0 0 0 0 0 0 0 0
1.8204 -1.1530 -1.7306 H 0 0 0 0 0 0 0 0 0 0 0 0
3.2110 0.1870 -0.2296 H 0 0 0 0 0 0 0 0 0 0 0 0
4.5907 -0.5555 -2.2342 H 0 0 0 0 0 0 0 0 0 0 0 0
6.0356 0.4287 -0.1028 H 0 0 0 0 0 0 0 0 0 0 0 0
8.1541 -0.6597 0.4715 H 0 0 0 0 0 0 0 0 0 0 0 0
8.5728 2.8593 -0.6039 H 0 0 0 0 0 0 0 0 0 0 0 0
10.0124 3.3199 0.3425 H 0 0 0 0 0 0 0 0 0 0 0 0
8.3815 3.0923 1.1172 H 0 0 0 0 0 0 0 0 0 0 0 0
8.1620 1.5477 2.2922 H 0 0 0 0 0 0 0 0 0 0 0 0
9.4975 0.2537 2.4641 H 0 0 0 0 0 0 0 0 0 0 0 0
9.8356 2.0786 2.4753 H 0 0 0 0 0 0 0 0 0 0 0 0
10.4885 0.2187 -1.6926 H 0 0 0 0 0 0 0 0 0 0 0 0
13.4972 -0.7470 -2.9680 H 0 0 0 0 0 0 0 0 0 0 0 0
11.8382 -0.0340 -3.2645 H 0 0 0 0 0 0 0 0 0 0 0 0
11.9725 -1.6547 -2.4846 H 0 0 0 0 0 0 0 0 0 0 0 0
14.0785 1.5856 -1.0902 H 0 0 0 0 0 0 0 0 0 0 0 0
12.5057 2.1405 -1.4653 H 0 0 0 0 0 0 0 0 0 0 0 0
13.4141 1.3176 -2.6827 H 0 0 0 0 0 0 0 0 0 0 0 0
14.5275 0.6770 -0.1131 H 0 0 0 0 0 0 0 0 0 0 0 0
16.8046 -0.5822 -0.8280 H 0 0 0 0 0 0 0 0 0 0 0 0
15.9243 -2.8146 0.0602 H 0 0 0 0 0 0 0 0 0 0 0 0
16.2470 -1.9725 1.6916 H 0 0 0 0 0 0 0 0 0 0 0 0
17.5280 -2.1253 0.5125 H 0 0 0 0 0 0 0 0 0 0 0 0
17.6782 0.3460 1.0083 H 0 0 0 0 0 0 0 0 0 0 0 0
16.2752 -0.1561 2.0910 H 0 0 0 0 0 0 0 0 0 0 0 0
15.1594 1.7594 1.5803 H 0 0 0 0 0 0 0 0 0 0 0 0
15.3673 3.2689 0.0649 H 0 0 0 0 0 0 0 0 0 0 0 0
16.1746 2.0826 -1.0101 H 0 0 0 0 0 0 0 0 0 0 0 0
17.1986 4.1124 -0.9516 H 0 0 0 0 0 0 0 0 0 0 0 0
17.5736 4.1636 0.7994 H 0 0 0 0 0 0 0 0 0 0 0 0
19.2876 3.5767 -0.6452 H 0 0 0 0 0 0 0 0 0 0 0 0
5.0017 1.3015 -2.6537 H 0 0 0 0 0 0 0 0 0 0 0 0
7.4380 2.4634 -3.1062 H 0 0 0 0 0 0 0 0 0 0 0 0
5.8647 3.3063 -3.1164 H 0 0 0 0 0 0 0 0 0 0 0 0
6.8777 3.5065 -1.6923 H 0 0 0 0 0 0 0 0 0 0 0 0
4.1132 2.6868 -0.9295 H 0 0 0 0 0 0 0 0 0 0 0 0
4.9302 1.4361 0.0614 H 0 0 0 0 0 0 0 0 0 0 0 0
5.7724 2.9417 -0.2228 H 0 0 0 0 0 0 0 0 0 0 0 0
2.3968 -1.9782 1.3399 H 0 0 0 0 0 0 0 0 0 0 0 0
1.8240 0.2952 2.5074 H 0 0 0 0 0 0 0 0 0 0 0 0
3.3113 0.9440 1.9171 H 0 0 0 0 0 0 0 0 0 0 0 0
1.9793 0.7062 0.7524 H 0 0 0 0 0 0 0 0 0 0 0 0
4.6509 -2.6036 1.8479 H 0 0 0 0 0 0 0 0 0 0 0 0
5.1624 -0.7786 1.9407 H 0 0 0 0 0 0 0 0 0 0 0 0
5.2294 -1.5091 3.9125 H 0 0 0 0 0 0 0 0 0 0 0 0
3.7669 -2.5221 3.8875 H 0 0 0 0 0 0 0 0 0 0 0 0
3.6317 -0.6584 3.8906 H 0 0 0 0 0 0 0 0 0 0 0 0
1 2 1 0 0 0 0
2 3 1 0 0 0 0
3 4 1 0 0 0 0
4 5 1 0 0 0 0
5 6 1 0 0 0 0
6 7 1 0 0 0 0
7 8 1 0 0 0 0
8 9 1 0 0 0 0
9 10 1 0 0 0 0
9 11 1 0 0 0 0
11 12 2 0 0 0 0
11 13 1 0 0 0 0
13 14 1 0 0 0 0
14 15 1 0 0 0 0
15 16 1 0 0 0 0
16 17 1 0 0 0 0
17 18 1 0 0 0 0
18 19 2 0 0 0 0
18 20 1 0 0 0 0
20 21 1 0 0 0 0
21 22 1 0 0 0 0
22 23 1 0 0 0 0
23 24 1 0 0 0 0
23 25 1 0 0 0 0
25 26 1 0 0 0 0
26 27 1 0 0 0 0
26 28 1 0 0 0 0
28 29 1 0 0 0 0
29 30 2 0 0 0 0
29 31 1 0 0 0 0
31 32 1 0 0 0 0
21 33 1 0 0 0 0
33 34 2 0 0 0 0
33 35 1 0 0 0 0
35 36 1 0 0 0 0
36 37 1 0 0 0 0
36 38 1 0 0 0 0
38 39 2 0 0 0 0
38 40 1 0 0 0 0
40 41 1 0 0 0 0
41 42 1 0 0 0 0
41 43 1 0 0 0 0
41 44 1 1 0 0 0
44 45 2 0 0 0 0
44 46 1 0 0 0 0
46 47 1 0 0 0 0
47 48 1 0 0 0 0
48 49 2 0 0 0 0
48 50 1 0 0 0 0
50 51 1 0 0 0 0
51 52 1 0 0 0 0
52 53 2 0 0 0 0
52 54 1 0 0 0 0
54 55 1 0 0 0 0
55 56 1 0 0 0 0
55 57 1 0 0 0 0
55 58 1 1 0 0 0
58 59 2 0 0 0 0
58 60 1 0 0 0 0
60 61 1 0 0 0 0
61 62 1 0 0 0 0
61 63 1 0 0 0 0
61 64 1 1 0 0 0
64 65 2 0 0 0 0
64 66 1 0 0 0 0
66 67 1 0 0 0 0
67 68 1 0 0 0 0
67 69 1 0 0 0 0
69 70 1 0 0 0 0
70 71 1 0 0 0 0
71 72 1 0 0 0 0
72 73 1 0 0 0 0
51 74 1 0 0 0 0
74 75 1 0 0 0 0
74 76 1 0 0 0 0
47 77 1 0 0 0 0
77 78 1 0 0 0 0
77 79 1 0 0 0 0
79 80 1 0 0 0 0
17 13 1 0 0 0 0
1 81 1 0 0 0 0
1 82 1 0 0 0 0
1 83 1 0 0 0 0
2 84 1 0 0 0 0
2 85 1 0 0 0 0
3 86 1 0 0 0 0
3 87 1 0 0 0 0
4 88 1 0 0 0 0
4 89 1 0 0 0 0
5 90 1 0 0 0 0
5 91 1 0 0 0 0
6 92 1 0 0 0 0
6 93 1 0 0 0 0
7 94 1 0 0 0 0
7 95 1 0 0 0 0
8 96 1 0 0 0 0
8 97 1 0 0 0 0
9 98 1 6 0 0 0
10 99 1 0 0 0 0
10100 1 0 0 0 0
10101 1 0 0 0 0
14102 1 0 0 0 0
14103 1 0 0 0 0
15104 1 0 0 0 0
15105 1 0 0 0 0
16106 1 0 0 0 0
16107 1 0 0 0 0
17108 1 6 0 0 0
20109 1 0 0 0 0
21110 1 6 0 0 0
22111 1 0 0 0 0
22112 1 0 0 0 0
23113 1 6 0 0 0
24114 1 0 0 0 0
24115 1 0 0 0 0
24116 1 0 0 0 0
25117 1 0 0 0 0
25118 1 0 0 0 0
26119 1 1 0 0 0
27120 1 0 0 0 0
28121 1 0 0 0 0
28122 1 0 0 0 0
31123 1 0 0 0 0
31124 1 0 0 0 0
32125 1 0 0 0 0
32126 1 0 0 0 0
32127 1 0 0 0 0
35128 1 0 0 0 0
36129 1 6 0 0 0
37130 1 0 0 0 0
37131 1 0 0 0 0
37132 1 0 0 0 0
40133 1 0 0 0 0
42134 1 0 0 0 0
42135 1 0 0 0 0
42136 1 0 0 0 0
43137 1 0 0 0 0
43138 1 0 0 0 0
43139 1 0 0 0 0
46140 1 0 0 0 0
47141 1 6 0 0 0
50142 1 0 0 0 0
51143 1 0 0 0 0
54144 1 0 0 0 0
56145 1 0 0 0 0
56146 1 0 0 0 0
56147 1 0 0 0 0
57148 1 0 0 0 0
57149 1 0 0 0 0
57150 1 0 0 0 0
60151 1 0 0 0 0
62152 1 0 0 0 0
62153 1 0 0 0 0
62154 1 0 0 0 0
63155 1 0 0 0 0
63156 1 0 0 0 0
63157 1 0 0 0 0
66158 1 0 0 0 0
67159 1 6 0 0 0
68160 1 0 0 0 0
68161 1 0 0 0 0
68162 1 0 0 0 0
69163 1 0 0 0 0
69164 1 0 0 0 0
70165 1 0 0 0 0
71166 1 0 0 0 0
71167 1 0 0 0 0
72168 1 0 0 0 0
72169 1 0 0 0 0
73170 1 0 0 0 0
74171 1 6 0 0 0
75172 1 0 0 0 0
75173 1 0 0 0 0
75174 1 0 0 0 0
76175 1 0 0 0 0
76176 1 0 0 0 0
76177 1 0 0 0 0
77178 1 6 0 0 0
78179 1 0 0 0 0
78180 1 0 0 0 0
78181 1 0 0 0 0
79182 1 0 0 0 0
79183 1 0 0 0 0
80184 1 0 0 0 0
80185 1 0 0 0 0
80186 1 0 0 0 0
M END
> <DATABASE_ID>
NP0003265
> <DATABASE_NAME>
NP-MRD
> <SMILES>
[H]OC([H])([H])C([H])([H])N([H])C([H])([H])[C@]([H])(N([H])C(=O)C(N([H])C(=O)C(N([H])C(=O)[C@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)C(N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@]([H])(N([H])C(=O)[C@@]1([H])N(C(=O)[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])C1([H])[H])C([H])([H])[C@@]([H])(C([H])([H])[H])C([H])([H])[C@@]([H])(O[H])C([H])([H])C(=O)C([H])([H])C([H])([H])[H])C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]
> <INCHI_IDENTIFIER>
InChI=1S/C58H106N10O12/c1-17-20-21-22-23-24-26-38(8)52(77)68-29-25-27-44(68)49(74)62-43(32-36(6)31-42(71)33-41(70)19-3)48(73)61-40(10)47(72)65-56(11,12)54(79)64-46(37(7)18-2)50(75)63-45(35(4)5)51(76)66-58(15,16)55(80)67-57(13,14)53(78)60-39(9)34-59-28-30-69/h35-40,42-46,59,69,71H,17-34H2,1-16H3,(H,60,78)(H,61,73)(H,62,74)(H,63,75)(H,64,79)(H,65,72)(H,66,76)(H,67,80)/t36-,37+,38+,39+,40-,42+,43+,44-,45+,46-/m0/s1
> <INCHI_KEY>
MBPYYBXSIMRVJP-UHFFFAOYSA-N
> <FORMULA>
C58H106N10O12
> <MOLECULAR_WEIGHT>
1135.544
> <EXACT_MASS>
1134.799168893
> <JCHEM_ACCEPTOR_COUNT>
13
> <JCHEM_ATOM_COUNT>
186
> <JCHEM_AVERAGE_POLARIZABILITY>
132.0074653172729
> <JCHEM_BIOAVAILABILITY>
0
> <JCHEM_DONOR_COUNT>
11
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
0
> <JCHEM_IUPAC>
(4R,6R)-6-hydroxy-N-[(1S)-1-[(1-{[(1S,2R)-1-{[(1S)-1-({1-[(1-{[(2R)-1-[(2-hydroxyethyl)amino]propan-2-yl]carbamoyl}-1-methylethyl)carbamoyl]-1-methylethyl}carbamoyl)-2-methylpropyl]carbamoyl}-2-methylbutyl]carbamoyl}-1-methylethyl)carbamoyl]ethyl]-4-methyl-2-({1-[(2R)-2-methyldecanoyl]pyrrolidin-2-yl}formamido)-8-oxodecanamide
> <ALOGPS_LOGP>
3.66
> <JCHEM_LOGP>
3.476255169333333
> <ALOGPS_LOGS>
-5.18
> <JCHEM_MDDR_LIKE_RULE>
0
> <JCHEM_NUMBER_OF_RINGS>
1
> <JCHEM_PHYSIOLOGICAL_CHARGE>
1
> <JCHEM_PKA>
12.000481789633653
> <JCHEM_PKA_STRONGEST_ACIDIC>
11.609000866293945
> <JCHEM_PKA_STRONGEST_BASIC>
9.181673875472335
> <JCHEM_POLAR_SURFACE_AREA>
322.6699999999999
> <JCHEM_REFRACTIVITY>
305.8424000000001
> <JCHEM_ROTATABLE_BOND_COUNT>
38
> <JCHEM_RULE_OF_FIVE>
0
> <ALOGPS_SOLUBILITY>
7.57e-03 g/l
> <JCHEM_TRADITIONAL_IUPAC>
(4R,6R)-6-hydroxy-N-[(1S)-1-[(1-{[(1S,2R)-1-{[(1S)-1-({1-[(1-{[(2R)-1-[(2-hydroxyethyl)amino]propan-2-yl]carbamoyl}-1-methylethyl)carbamoyl]-1-methylethyl}carbamoyl)-2-methylpropyl]carbamoyl}-2-methylbutyl]carbamoyl}-1-methylethyl)carbamoyl]ethyl]-4-methyl-2-({1-[(2R)-2-methyldecanoyl]pyrrolidin-2-yl}formamido)-8-oxodecanamide
> <JCHEM_VEBER_RULE>
0
$$$$
3D-SDF for NP0003265 (Roseoferin B2)
RDKit 3D
186186 0 0 0 0 0 0 0 0999 V2000
-14.4159 5.8769 0.9783 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.0110 5.2324 -0.3022 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.6540 3.8490 -0.5206 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.3571 2.9575 0.6359 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.7353 1.5394 0.5293 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.7402 0.6149 1.3136 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.5184 0.5625 0.3893 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.8963 1.8689 0.2027 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.0832 1.9148 -1.0880 C 0 0 1 0 0 0 0 0 0 0 0 0
-10.7442 3.4728 -1.3027 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.9752 1.1213 -1.2056 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.2986 1.4221 0.2103 O 0 0 0 0 0 0 0 0 0 0 0 0
-9.0752 0.2930 -1.6555 N 0 0 0 0 0 0 0 0 0 0 0 0
-9.6486 -0.5211 -2.8765 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.5254 -0.5277 -3.8350 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.3947 0.2153 -3.1689 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.8159 -0.1674 -1.6192 C 0 0 1 0 0 0 0 0 0 0 0 0
-6.6075 0.0435 -0.9004 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.6536 0.7268 -1.3877 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.4633 -0.5541 0.3880 N 0 0 0 0 0 0 0 0 0 0 0 0
-5.2129 -0.6106 0.9776 C 0 0 2 0 0 0 0 0 0 0 0 0
-5.1326 -1.7551 1.9824 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.7247 -3.0127 1.2898 C 0 0 1 0 0 0 0 0 0 0 0 0
-4.8768 -3.4630 0.1388 C 0 0 0 0 0 0 0 0 0 0 0 0
-6.0758 -4.0495 2.2951 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.2223 -4.8791 1.8266 C 0 0 1 0 0 0 0 0 0 0 0 0
-8.2944 -3.8597 1.7815 O 0 0 0 0 0 0 0 0 0 0 0 0
-7.2369 -5.3819 0.4217 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.5734 -6.1173 0.2690 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.4261 -6.0015 1.0323 O 0 0 0 0 0 0 0 0 0 0 0 0
-8.6977 -6.9642 -0.9861 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.6061 -8.0249 -0.8318 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.1766 0.3053 0.8591 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.7015 0.4758 -0.4412 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.5740 1.0632 1.8047 N 0 0 0 0 0 0 0 0 0 0 0 0
-2.3023 1.7577 1.3230 C 0 0 1 0 0 0 0 0 0 0 0 0
-1.7691 2.2877 2.5967 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6109 0.3986 0.9351 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6705 -0.4395 1.9599 O 0 0 0 0 0 0 0 0 0 0 0 0
-1.0705 0.1161 -0.2189 N 0 0 0 0 0 0 0 0 0 0 0 0
-0.4564 -0.9862 -0.8945 C 0 0 1 0 0 0 0 0 0 0 0 0
-1.2142 -2.2573 -0.9445 C 0 0 0 0 0 0 0 0 0 0 0 0
0.0428 -0.5381 -2.2179 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8125 -1.2758 0.0516 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4709 -1.4725 1.2404 O 0 0 0 0 0 0 0 0 0 0 0 0
1.9957 -1.1866 -0.5716 N 0 0 0 0 0 0 0 0 0 0 0 0
3.2957 -1.1579 -0.4237 C 0 0 1 0 0 0 0 0 0 0 0 0
4.6572 -1.1768 -0.1698 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6087 -1.3782 0.3937 O 0 0 0 0 0 0 0 0 0 0 0 0
5.2291 -0.3941 -1.5821 N 0 0 0 0 0 0 0 0 0 0 0 0
6.4682 0.2010 -1.3264 C 0 0 0 0 0 0 0 0 0 0 0 0
7.6421 0.7638 -1.0718 C 0 0 0 0 0 0 0 0 0 0 0 0
8.3080 1.6489 -1.5993 O 0 0 0 0 0 0 0 0 0 0 0 0
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M END
PDB for NP0003265 (Roseoferin B2)HEADER PROTEIN 01-JUL-21 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 01-JUL-21 0 HETATM 1 C UNK 0 -14.416 5.877 0.978 0.00 0.00 C+0 HETATM 2 C UNK 0 -14.011 5.232 -0.302 0.00 0.00 C+0 HETATM 3 C UNK 0 -14.654 3.849 -0.521 0.00 0.00 C+0 HETATM 4 C UNK 0 -14.357 2.958 0.636 0.00 0.00 C+0 HETATM 5 C UNK 0 -14.735 1.539 0.529 0.00 0.00 C+0 HETATM 6 C UNK 0 -13.740 0.615 1.314 0.00 0.00 C+0 HETATM 7 C UNK 0 -12.518 0.563 0.389 0.00 0.00 C+0 HETATM 8 C UNK 0 -11.896 1.869 0.203 0.00 0.00 C+0 HETATM 9 C UNK 0 -11.083 1.915 -1.088 0.00 0.00 C+0 HETATM 10 C UNK 0 -10.744 3.473 -1.303 0.00 0.00 C+0 HETATM 11 C UNK 0 -9.975 1.121 -1.206 0.00 0.00 C+0 HETATM 12 O UNK 0 -9.299 1.422 0.210 0.00 0.00 O+0 HETATM 13 N UNK 0 -9.075 0.293 -1.656 0.00 0.00 N+0 HETATM 14 C UNK 0 -9.649 -0.521 -2.877 0.00 0.00 C+0 HETATM 15 C UNK 0 -8.525 -0.528 -3.835 0.00 0.00 C+0 HETATM 16 C UNK 0 -7.395 0.215 -3.169 0.00 0.00 C+0 HETATM 17 C UNK 0 -7.816 -0.167 -1.619 0.00 0.00 C+0 HETATM 18 C UNK 0 -6.607 0.044 -0.900 0.00 0.00 C+0 HETATM 19 O UNK 0 -5.654 0.727 -1.388 0.00 0.00 O+0 HETATM 20 N UNK 0 -6.463 -0.554 0.388 0.00 0.00 N+0 HETATM 21 C UNK 0 -5.213 -0.611 0.978 0.00 0.00 C+0 HETATM 22 C UNK 0 -5.133 -1.755 1.982 0.00 0.00 C+0 HETATM 23 C UNK 0 -5.725 -3.013 1.290 0.00 0.00 C+0 HETATM 24 C UNK 0 -4.877 -3.463 0.139 0.00 0.00 C+0 HETATM 25 C UNK 0 -6.076 -4.050 2.295 0.00 0.00 C+0 HETATM 26 C UNK 0 -7.222 -4.879 1.827 0.00 0.00 C+0 HETATM 27 O UNK 0 -8.294 -3.860 1.782 0.00 0.00 O+0 HETATM 28 C UNK 0 -7.237 -5.382 0.422 0.00 0.00 C+0 HETATM 29 C UNK 0 -8.573 -6.117 0.269 0.00 0.00 C+0 HETATM 30 O UNK 0 -9.426 -6.002 1.032 0.00 0.00 O+0 HETATM 31 C UNK 0 -8.698 -6.964 -0.986 0.00 0.00 C+0 HETATM 32 C UNK 0 -7.606 -8.025 -0.832 0.00 0.00 C+0 HETATM 33 C UNK 0 -4.177 0.305 0.859 0.00 0.00 C+0 HETATM 34 O UNK 0 -3.701 0.476 -0.441 0.00 0.00 O+0 HETATM 35 N UNK 0 -3.574 1.063 1.805 0.00 0.00 N+0 HETATM 36 C UNK 0 -2.302 1.758 1.323 0.00 0.00 C+0 HETATM 37 C UNK 0 -1.769 2.288 2.597 0.00 0.00 C+0 HETATM 38 C UNK 0 -1.611 0.399 0.935 0.00 0.00 C+0 HETATM 39 O UNK 0 -1.671 -0.440 1.960 0.00 0.00 O+0 HETATM 40 N UNK 0 -1.071 0.116 -0.219 0.00 0.00 N+0 HETATM 41 C UNK 0 -0.456 -0.986 -0.895 0.00 0.00 C+0 HETATM 42 C UNK 0 -1.214 -2.257 -0.945 0.00 0.00 C+0 HETATM 43 C UNK 0 0.043 -0.538 -2.218 0.00 0.00 C+0 HETATM 44 C UNK 0 0.813 -1.276 0.052 0.00 0.00 C+0 HETATM 45 O UNK 0 0.471 -1.472 1.240 0.00 0.00 O+0 HETATM 46 N UNK 0 1.996 -1.187 -0.572 0.00 0.00 N+0 HETATM 47 C UNK 0 3.296 -1.158 -0.424 0.00 0.00 C+0 HETATM 48 C UNK 0 4.657 -1.177 -0.170 0.00 0.00 C+0 HETATM 49 O UNK 0 5.609 -1.378 0.394 0.00 0.00 O+0 HETATM 50 N UNK 0 5.229 -0.394 -1.582 0.00 0.00 N+0 HETATM 51 C UNK 0 6.468 0.201 -1.326 0.00 0.00 C+0 HETATM 52 C UNK 0 7.642 0.764 -1.072 0.00 0.00 C+0 HETATM 53 O UNK 0 8.308 1.649 -1.599 0.00 0.00 O+0 HETATM 54 N UNK 0 8.468 0.210 0.215 0.00 0.00 N+0 HETATM 55 C UNK 0 9.414 1.230 0.556 0.00 0.00 C+0 HETATM 56 C UNK 0 9.070 2.656 0.306 0.00 0.00 C+0 HETATM 57 C UNK 0 9.205 1.252 2.200 0.00 0.00 C+0 HETATM 58 C UNK 0 10.760 0.747 0.388 0.00 0.00 C+0 HETATM 59 O UNK 0 11.593 0.666 1.311 0.00 0.00 O+0 HETATM 60 N UNK 0 11.251 0.321 -0.920 0.00 0.00 N+0 HETATM 61 C UNK 0 12.522 0.017 -1.160 0.00 0.00 C+0 HETATM 62 C UNK 0 12.402 -0.687 -2.668 0.00 0.00 C+0 HETATM 63 C UNK 0 13.240 1.284 -1.605 0.00 0.00 C+0 HETATM 64 C UNK 0 13.494 -0.982 -0.637 0.00 0.00 C+0 HETATM 65 O UNK 0 13.224 -2.169 -0.517 0.00 0.00 O+0 HETATM 66 N UNK 0 14.791 -0.467 -0.319 0.00 0.00 N+0 HETATM 67 C UNK 0 16.092 -0.651 -0.011 0.00 0.00 C+0 HETATM 68 C UNK 0 16.406 -2.033 0.611 0.00 0.00 C+0 HETATM 69 C UNK 0 16.525 0.296 1.158 0.00 0.00 C+0 HETATM 70 N UNK 0 16.056 1.592 0.963 0.00 0.00 N+0 HETATM 71 C UNK 0 16.264 2.558 0.080 0.00 0.00 C+0 HETATM 72 C UNK 0 17.453 3.423 -0.060 0.00 0.00 C+0 HETATM 73 O UNK 0 18.660 2.838 -0.325 0.00 0.00 O+0 HETATM 74 C UNK 0 5.740 1.624 -1.951 0.00 0.00 C+0 HETATM 75 C UNK 0 6.606 2.686 -2.370 0.00 0.00 C+0 HETATM 76 C UNK 0 5.031 2.172 -0.703 0.00 0.00 C+0 HETATM 77 C UNK 0 3.070 -1.108 1.417 0.00 0.00 C+0 HETATM 78 C UNK 0 2.465 0.184 1.632 0.00 0.00 C+0 HETATM 79 C UNK 0 4.304 -1.519 2.021 0.00 0.00 C+0 HETATM 80 C UNK 0 4.172 -1.548 3.587 0.00 0.00 C+0 HETATM 81 H UNK 0 -15.259 5.444 1.498 0.00 0.00 H+0 HETATM 82 H UNK 0 -14.531 6.958 0.887 0.00 0.00 H+0 HETATM 83 H UNK 0 -13.483 5.778 1.652 0.00 0.00 H+0 HETATM 84 H UNK 0 -12.923 5.138 -0.394 0.00 0.00 H+0 HETATM 85 H UNK 0 -14.356 5.881 -1.156 0.00 0.00 H+0 HETATM 86 H UNK 0 -15.701 3.916 -0.799 0.00 0.00 H+0 HETATM 87 H UNK 0 -14.150 3.368 -1.415 0.00 0.00 H+0 HETATM 88 H UNK 0 -13.667 3.278 1.403 0.00 0.00 H+0 HETATM 89 H UNK 0 -15.363 3.315 1.359 0.00 0.00 H+0 HETATM 90 H UNK 0 -14.625 1.211 -0.568 0.00 0.00 H+0 HETATM 91 H UNK 0 -15.745 1.244 0.793 0.00 0.00 H+0 HETATM 92 H UNK 0 -14.124 -0.385 1.391 0.00 0.00 H+0 HETATM 93 H UNK 0 -13.551 1.081 2.256 0.00 0.00 H+0 HETATM 94 H UNK 0 -11.859 -0.258 0.718 0.00 0.00 H+0 HETATM 95 H UNK 0 -12.911 0.176 -0.613 0.00 0.00 H+0 HETATM 96 H UNK 0 -12.163 2.828 0.478 0.00 0.00 H+0 HETATM 97 H UNK 0 -10.956 1.736 1.054 0.00 0.00 H+0 HETATM 98 H UNK 0 -11.868 1.760 -1.901 0.00 0.00 H+0 HETATM 99 H UNK 0 -11.752 3.828 -1.688 0.00 0.00 H+0 HETATM 100 H UNK 0 -9.978 3.484 -2.056 0.00 0.00 H+0 HETATM 101 H UNK 0 -10.476 3.816 -0.315 0.00 0.00 H+0 HETATM 102 H UNK 0 -9.716 -1.507 -2.382 0.00 0.00 H+0 HETATM 103 H UNK 0 -10.531 -0.047 -3.184 0.00 0.00 H+0 HETATM 104 H UNK 0 -8.771 -0.127 -4.812 0.00 0.00 H+0 HETATM 105 H UNK 0 -8.109 -1.588 -3.981 0.00 0.00 H+0 HETATM 106 H UNK 0 -7.531 1.304 -3.131 0.00 0.00 H+0 HETATM 107 H UNK 0 -6.388 -0.165 -3.243 0.00 0.00 H+0 HETATM 108 H UNK 0 -7.896 -1.333 -1.768 0.00 0.00 H+0 HETATM 109 H UNK 0 -7.363 -0.831 0.881 0.00 0.00 H+0 HETATM 110 H UNK 0 -4.730 -1.412 0.022 0.00 0.00 H+0 HETATM 111 H UNK 0 -5.499 -1.613 2.975 0.00 0.00 H+0 HETATM 112 H UNK 0 -3.990 -2.005 2.053 0.00 0.00 H+0 HETATM 113 H UNK 0 -6.662 -2.656 0.851 0.00 0.00 H+0 HETATM 114 H UNK 0 -4.749 -4.576 0.266 0.00 0.00 H+0 HETATM 115 H UNK 0 -5.259 -3.274 -0.857 0.00 0.00 H+0 HETATM 116 H UNK 0 -3.790 -3.088 0.182 0.00 0.00 H+0 HETATM 117 H UNK 0 -6.256 -3.672 3.319 0.00 0.00 H+0 HETATM 118 H UNK 0 -5.182 -4.720 2.397 0.00 0.00 H+0 HETATM 119 H UNK 0 -7.474 -5.644 2.546 0.00 0.00 H+0 HETATM 120 H UNK 0 -8.755 -3.915 2.632 0.00 0.00 H+0 HETATM 121 H UNK 0 -7.305 -4.539 -0.311 0.00 0.00 H+0 HETATM 122 H UNK 0 -6.495 -6.055 0.094 0.00 0.00 H+0 HETATM 123 H UNK 0 -9.690 -7.409 -1.013 0.00 0.00 H+0 HETATM 124 H UNK 0 -8.547 -6.297 -1.815 0.00 0.00 H+0 HETATM 125 H UNK 0 -7.382 -8.159 0.234 0.00 0.00 H+0 HETATM 126 H UNK 0 -6.680 -7.617 -1.356 0.00 0.00 H+0 HETATM 127 H UNK 0 -7.963 -8.907 -1.329 0.00 0.00 H+0 HETATM 128 H UNK 0 -3.906 1.248 2.752 0.00 0.00 H+0 HETATM 129 H UNK 0 -2.401 2.284 0.473 0.00 0.00 H+0 HETATM 130 H UNK 0 -0.808 2.759 2.623 0.00 0.00 H+0 HETATM 131 H UNK 0 -1.772 1.440 3.391 0.00 0.00 H+0 HETATM 132 H UNK 0 -2.540 3.043 2.956 0.00 0.00 H+0 HETATM 133 H UNK 0 -1.056 1.034 -0.932 0.00 0.00 H+0 HETATM 134 H UNK 0 -2.125 -2.072 -1.465 0.00 0.00 H+0 HETATM 135 H UNK 0 -0.577 -2.963 -1.536 0.00 0.00 H+0 HETATM 136 H UNK 0 -1.346 -2.713 0.031 0.00 0.00 H+0 HETATM 137 H UNK 0 0.372 -1.377 -2.872 0.00 0.00 H+0 HETATM 138 H UNK 0 0.791 0.297 -2.115 0.00 0.00 H+0 HETATM 139 H UNK 0 -0.816 0.008 -2.760 0.00 0.00 H+0 HETATM 140 H UNK 0 1.820 -1.153 -1.731 0.00 0.00 H+0 HETATM 141 H UNK 0 3.211 0.187 -0.230 0.00 0.00 H+0 HETATM 142 H UNK 0 4.591 -0.556 -2.234 0.00 0.00 H+0 HETATM 143 H UNK 0 6.036 0.429 -0.103 0.00 0.00 H+0 HETATM 144 H UNK 0 8.154 -0.660 0.472 0.00 0.00 H+0 HETATM 145 H UNK 0 8.573 2.859 -0.604 0.00 0.00 H+0 HETATM 146 H UNK 0 10.012 3.320 0.343 0.00 0.00 H+0 HETATM 147 H UNK 0 8.382 3.092 1.117 0.00 0.00 H+0 HETATM 148 H UNK 0 8.162 1.548 2.292 0.00 0.00 H+0 HETATM 149 H UNK 0 9.498 0.254 2.464 0.00 0.00 H+0 HETATM 150 H UNK 0 9.836 2.079 2.475 0.00 0.00 H+0 HETATM 151 H UNK 0 10.489 0.219 -1.693 0.00 0.00 H+0 HETATM 152 H UNK 0 13.497 -0.747 -2.968 0.00 0.00 H+0 HETATM 153 H UNK 0 11.838 -0.034 -3.264 0.00 0.00 H+0 HETATM 154 H UNK 0 11.973 -1.655 -2.485 0.00 0.00 H+0 HETATM 155 H UNK 0 14.079 1.586 -1.090 0.00 0.00 H+0 HETATM 156 H UNK 0 12.506 2.140 -1.465 0.00 0.00 H+0 HETATM 157 H UNK 0 13.414 1.318 -2.683 0.00 0.00 H+0 HETATM 158 H UNK 0 14.527 0.677 -0.113 0.00 0.00 H+0 HETATM 159 H UNK 0 16.805 -0.582 -0.828 0.00 0.00 H+0 HETATM 160 H UNK 0 15.924 -2.815 0.060 0.00 0.00 H+0 HETATM 161 H UNK 0 16.247 -1.972 1.692 0.00 0.00 H+0 HETATM 162 H UNK 0 17.528 -2.125 0.513 0.00 0.00 H+0 HETATM 163 H UNK 0 17.678 0.346 1.008 0.00 0.00 H+0 HETATM 164 H UNK 0 16.275 -0.156 2.091 0.00 0.00 H+0 HETATM 165 H UNK 0 15.159 1.759 1.580 0.00 0.00 H+0 HETATM 166 H UNK 0 15.367 3.269 0.065 0.00 0.00 H+0 HETATM 167 H UNK 0 16.175 2.083 -1.010 0.00 0.00 H+0 HETATM 168 H UNK 0 17.199 4.112 -0.952 0.00 0.00 H+0 HETATM 169 H UNK 0 17.574 4.164 0.799 0.00 0.00 H+0 HETATM 170 H UNK 0 19.288 3.577 -0.645 0.00 0.00 H+0 HETATM 171 H UNK 0 5.002 1.302 -2.654 0.00 0.00 H+0 HETATM 172 H UNK 0 7.438 2.463 -3.106 0.00 0.00 H+0 HETATM 173 H UNK 0 5.865 3.306 -3.116 0.00 0.00 H+0 HETATM 174 H UNK 0 6.878 3.506 -1.692 0.00 0.00 H+0 HETATM 175 H UNK 0 4.113 2.687 -0.930 0.00 0.00 H+0 HETATM 176 H UNK 0 4.930 1.436 0.061 0.00 0.00 H+0 HETATM 177 H UNK 0 5.772 2.942 -0.223 0.00 0.00 H+0 HETATM 178 H UNK 0 2.397 -1.978 1.340 0.00 0.00 H+0 HETATM 179 H UNK 0 1.824 0.295 2.507 0.00 0.00 H+0 HETATM 180 H UNK 0 3.311 0.944 1.917 0.00 0.00 H+0 HETATM 181 H UNK 0 1.979 0.706 0.752 0.00 0.00 H+0 HETATM 182 H UNK 0 4.651 -2.604 1.848 0.00 0.00 H+0 HETATM 183 H UNK 0 5.162 -0.779 1.941 0.00 0.00 H+0 HETATM 184 H UNK 0 5.229 -1.509 3.913 0.00 0.00 H+0 HETATM 185 H UNK 0 3.767 -2.522 3.888 0.00 0.00 H+0 HETATM 186 H UNK 0 3.632 -0.658 3.891 0.00 0.00 H+0 CONECT 1 2 81 82 83 CONECT 2 1 3 84 85 CONECT 3 2 4 86 87 CONECT 4 3 5 88 89 CONECT 5 4 6 90 91 CONECT 6 5 7 92 93 CONECT 7 6 8 94 95 CONECT 8 7 9 96 97 CONECT 9 8 10 11 98 CONECT 10 9 99 100 101 CONECT 11 9 12 13 CONECT 12 11 CONECT 13 11 14 17 CONECT 14 13 15 102 103 CONECT 15 14 16 104 105 CONECT 16 15 17 106 107 CONECT 17 16 18 13 108 CONECT 18 17 19 20 CONECT 19 18 CONECT 20 18 21 109 CONECT 21 20 22 33 110 CONECT 22 21 23 111 112 CONECT 23 22 24 25 113 CONECT 24 23 114 115 116 CONECT 25 23 26 117 118 CONECT 26 25 27 28 119 CONECT 27 26 120 CONECT 28 26 29 121 122 CONECT 29 28 30 31 CONECT 30 29 CONECT 31 29 32 123 124 CONECT 32 31 125 126 127 CONECT 33 21 34 35 CONECT 34 33 CONECT 35 33 36 128 CONECT 36 35 37 38 129 CONECT 37 36 130 131 132 CONECT 38 36 39 40 CONECT 39 38 CONECT 40 38 41 133 CONECT 41 40 42 43 44 CONECT 42 41 134 135 136 CONECT 43 41 137 138 139 CONECT 44 41 45 46 CONECT 45 44 CONECT 46 44 47 140 CONECT 47 46 48 77 141 CONECT 48 47 49 50 CONECT 49 48 CONECT 50 48 51 142 CONECT 51 50 52 74 143 CONECT 52 51 53 54 CONECT 53 52 CONECT 54 52 55 144 CONECT 55 54 56 57 58 CONECT 56 55 145 146 147 CONECT 57 55 148 149 150 CONECT 58 55 59 60 CONECT 59 58 CONECT 60 58 61 151 CONECT 61 60 62 63 64 CONECT 62 61 152 153 154 CONECT 63 61 155 156 157 CONECT 64 61 65 66 CONECT 65 64 CONECT 66 64 67 158 CONECT 67 66 68 69 159 CONECT 68 67 160 161 162 CONECT 69 67 70 163 164 CONECT 70 69 71 165 CONECT 71 70 72 166 167 CONECT 72 71 73 168 169 CONECT 73 72 170 CONECT 74 51 75 76 171 CONECT 75 74 172 173 174 CONECT 76 74 175 176 177 CONECT 77 47 78 79 178 CONECT 78 77 179 180 181 CONECT 79 77 80 182 183 CONECT 80 79 184 185 186 CONECT 81 1 CONECT 82 1 CONECT 83 1 CONECT 84 2 CONECT 85 2 CONECT 86 3 CONECT 87 3 CONECT 88 4 CONECT 89 4 CONECT 90 5 CONECT 91 5 CONECT 92 6 CONECT 93 6 CONECT 94 7 CONECT 95 7 CONECT 96 8 CONECT 97 8 CONECT 98 9 CONECT 99 10 CONECT 100 10 CONECT 101 10 CONECT 102 14 CONECT 103 14 CONECT 104 15 CONECT 105 15 CONECT 106 16 CONECT 107 16 CONECT 108 17 CONECT 109 20 CONECT 110 21 CONECT 111 22 CONECT 112 22 CONECT 113 23 CONECT 114 24 CONECT 115 24 CONECT 116 24 CONECT 117 25 CONECT 118 25 CONECT 119 26 CONECT 120 27 CONECT 121 28 CONECT 122 28 CONECT 123 31 CONECT 124 31 CONECT 125 32 CONECT 126 32 CONECT 127 32 CONECT 128 35 CONECT 129 36 CONECT 130 37 CONECT 131 37 CONECT 132 37 CONECT 133 40 CONECT 134 42 CONECT 135 42 CONECT 136 42 CONECT 137 43 CONECT 138 43 CONECT 139 43 CONECT 140 46 CONECT 141 47 CONECT 142 50 CONECT 143 51 CONECT 144 54 CONECT 145 56 CONECT 146 56 CONECT 147 56 CONECT 148 57 CONECT 149 57 CONECT 150 57 CONECT 151 60 CONECT 152 62 CONECT 153 62 CONECT 154 62 CONECT 155 63 CONECT 156 63 CONECT 157 63 CONECT 158 66 CONECT 159 67 CONECT 160 68 CONECT 161 68 CONECT 162 68 CONECT 163 69 CONECT 164 69 CONECT 165 70 CONECT 166 71 CONECT 167 71 CONECT 168 72 CONECT 169 72 CONECT 170 73 CONECT 171 74 CONECT 172 75 CONECT 173 75 CONECT 174 75 CONECT 175 76 CONECT 176 76 CONECT 177 76 CONECT 178 77 CONECT 179 78 CONECT 180 78 CONECT 181 78 CONECT 182 79 CONECT 183 79 CONECT 184 80 CONECT 185 80 CONECT 186 80 MASTER 0 0 0 0 0 0 0 0 186 0 372 0 END SMILES for NP0003265 (Roseoferin B2)[H]OC([H])([H])C([H])([H])N([H])C([H])([H])[C@]([H])(N([H])C(=O)C(N([H])C(=O)C(N([H])C(=O)[C@]([H])(N([H])C(=O)[C@@]([H])(N([H])C(=O)C(N([H])C(=O)[C@@]([H])(N([H])C(=O)[C@]([H])(N([H])C(=O)[C@@]1([H])N(C(=O)[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])C1([H])[H])C([H])([H])[C@@]([H])(C([H])([H])[H])C([H])([H])[C@@]([H])(O[H])C([H])([H])C(=O)C([H])([H])C([H])([H])[H])C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])[C@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] INCHI for NP0003265 (Roseoferin B2)InChI=1S/C58H106N10O12/c1-17-20-21-22-23-24-26-38(8)52(77)68-29-25-27-44(68)49(74)62-43(32-36(6)31-42(71)33-41(70)19-3)48(73)61-40(10)47(72)65-56(11,12)54(79)64-46(37(7)18-2)50(75)63-45(35(4)5)51(76)66-58(15,16)55(80)67-57(13,14)53(78)60-39(9)34-59-28-30-69/h35-40,42-46,59,69,71H,17-34H2,1-16H3,(H,60,78)(H,61,73)(H,62,74)(H,63,75)(H,64,79)(H,65,72)(H,66,76)(H,67,80)/t36-,37+,38+,39+,40-,42+,43+,44-,45+,46-/m0/s1 3D Structure for NP0003265 (Roseoferin B2) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms |
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| Chemical Formula | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Average Mass | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Monoisotopic Mass | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| IUPAC Name | (4R,6R)-6-hydroxy-N-[(1S)-1-[(1-{[(1S,2R)-1-{[(1S)-1-({1-[(1-{[(2R)-1-[(2-hydroxyethyl)amino]propan-2-yl]carbamoyl}-1-methylethyl)carbamoyl]-1-methylethyl}carbamoyl)-2-methylpropyl]carbamoyl}-2-methylbutyl]carbamoyl}-1-methylethyl)carbamoyl]ethyl]-4-methyl-2-({1-[(2R)-2-methyldecanoyl]pyrrolidin-2-yl}formamido)-8-oxodecanamide | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Traditional Name | (4R,6R)-6-hydroxy-N-[(1S)-1-[(1-{[(1S,2R)-1-{[(1S)-1-({1-[(1-{[(2R)-1-[(2-hydroxyethyl)amino]propan-2-yl]carbamoyl}-1-methylethyl)carbamoyl]-1-methylethyl}carbamoyl)-2-methylpropyl]carbamoyl}-2-methylbutyl]carbamoyl}-1-methylethyl)carbamoyl]ethyl]-4-methyl-2-({1-[(2R)-2-methyldecanoyl]pyrrolidin-2-yl}formamido)-8-oxodecanamide | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| SMILES | CCCCCCCCC(C)C(=O)N1CCCC1C(=O)NC(CC(C)CC(O)CC(=O)CC)C(=O)NC(C)C(=O)NC(C)(C)C(=O)NC(C(C)CC)C(=O)NC(C(C)C)C(=O)NC(C)(C)C(=O)NC(C)(C)C(=O)NC(C)CNCCO | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Identifier | InChI=1S/C58H106N10O12/c1-17-20-21-22-23-24-26-38(8)52(77)68-29-25-27-44(68)49(74)62-43(32-36(6)31-42(71)33-41(70)19-3)48(73)61-40(10)47(72)65-56(11,12)54(79)64-46(37(7)18-2)50(75)63-45(35(4)5)51(76)66-58(15,16)55(80)67-57(13,14)53(78)60-39(9)34-59-28-30-69/h35-40,42-46,59,69,71H,17-34H2,1-16H3,(H,60,78)(H,61,73)(H,62,74)(H,63,75)(H,64,79)(H,65,72)(H,66,76)(H,67,80) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Key | MBPYYBXSIMRVJP-UHFFFAOYSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predicted Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Chemical Shift Submissions | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species of Origin |
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| Chemical Taxonomy | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Classification | Not classified | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Physical Properties | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| State | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Properties |
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| Predicted Properties |
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| External Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| NPAtlas ID | NPA011716 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HMDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DrugBank ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Phenol Explorer Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| FoodDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| KNApSAcK ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemspider ID | 78444825 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| KEGG Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BioCyc ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BiGG ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wikipedia Link | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| METLIN ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| PubChem Compound | 85221374 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| PDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| ChEBI ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Good Scents ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| General References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
