Showing NP-Card for Roseoferin C2 (NP0003268)
| Record Information | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Version | 2.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Created at | 2020-12-09 00:32:32 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Updated at | 2021-07-15 16:45:58 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| NP-MRD ID | NP0003268 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Common Name | Roseoferin C2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Provided By | NPAtlas | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | Roseoferin C2 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)(methyl)amino]propan-2-yl}-C-hydroxycarbonimidoyl)-1-methylethyl]-C-hydroxycarbonimidoyl}-1-methylethyl)-C-hydroxycarbonimidoyl]-2-methylbutyl}-C-hydroxycarbonimidoyl)-2-methylpropyl]-C-hydroxycarbonimidoyl}-2-methylpropyl)-C-hydroxycarbonimidoyl]ethyl}-4-methyl-8-oxodecanimidic acid. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structure |  MOL for NP0003268 (Roseoferin C2)
Mrv1652307012117083D
192192 0 0 0 0 999 V2000
-18.0677 -0.0325 -0.7160 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.6174 0.7049 -1.9220 C 0 0 1 0 0 0 0 0 0 0 0 0
-16.3538 0.2039 -2.5091 C 0 0 2 0 0 0 0 0 0 0 0 0
-15.0824 0.2997 -1.7437 C 0 0 2 0 0 0 0 0 0 0 0 0
-14.9745 -0.3673 -0.4534 C 0 0 1 0 0 0 0 0 0 0 0 0
-13.6873 -0.3634 0.2769 C 0 0 1 0 0 0 0 0 0 0 0 0
-13.0435 0.8231 0.7883 C 0 0 2 0 0 0 0 0 0 0 0 0
-12.6436 1.9592 -0.0386 C 0 0 1 0 0 0 0 0 0 0 0 0
-11.7538 1.7422 -1.1832 C 0 0 1 0 0 0 0 0 0 0 0 0
-11.4475 3.0887 -1.8712 C 0 0 0 0 0 0 0 0 0 0 0 0
-10.4398 1.1269 -0.8777 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.9984 1.0283 0.2915 O 0 0 0 0 0 0 0 0 0 0 0 0
-9.6513 0.6279 -1.9583 N 0 0 0 0 0 0 0 0 0 0 0 0
-10.1222 0.6325 -3.3339 C 0 0 1 0 0 0 0 0 0 0 0 0
-8.9277 0.1207 -4.1330 C 0 0 2 0 0 0 0 0 0 0 0 0
-7.7574 0.5905 -3.2351 C 0 0 2 0 0 0 0 0 0 0 0 0
-8.3490 0.0749 -1.9032 C 0 0 1 0 0 0 0 0 0 0 0 0
-7.4852 0.5687 -0.7870 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.6946 1.7203 -0.4029 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.4845 -0.2568 -0.1988 N 0 0 0 0 0 0 0 0 0 0 0 0
-5.7295 0.3063 0.9332 C 0 0 2 0 0 0 0 0 0 0 0 0
-6.6976 0.6350 1.9924 C 0 0 1 0 0 0 0 0 0 0 0 0
-7.3042 -0.5595 2.7087 C 0 0 2 0 0 0 0 0 0 0 0 0
-6.0951 -1.0990 3.5901 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.5497 -1.7708 1.7833 C 0 0 2 0 0 0 0 0 0 0 0 0
-8.1552 -2.9014 2.5132 C 0 0 1 0 0 0 0 0 0 0 0 0
-7.4943 -3.3380 3.6657 O 0 0 0 0 0 0 0 0 0 0 0 0
-9.5282 -3.3380 2.2948 C 0 0 1 0 0 0 0 0 0 0 0 0
-10.6329 -2.3848 2.4443 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.3437 -2.0898 1.5324 O 0 0 0 0 0 0 0 0 0 0 0 0
-10.9071 -1.7355 3.7916 C 0 0 2 0 0 0 0 0 0 0 0 0
-11.7744 -2.6649 4.6256 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.7722 1.2712 0.4983 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.7390 1.6538 -0.7410 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.7996 1.8660 1.3266 N 0 0 0 0 0 0 0 0 0 0 0 0
-2.7887 2.7974 0.7834 C 0 0 1 0 0 0 0 0 0 0 0 0
-2.8334 4.0632 1.6167 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4670 2.1027 0.9007 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4159 1.0041 1.4889 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.2670 2.6468 0.3712 N 0 0 0 0 0 0 0 0 0 0 0 0
0.9657 1.8549 0.5850 C 0 0 1 0 0 0 0 0 0 0 0 0
1.4794 1.4283 -0.7327 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9681 1.8843 -1.7734 O 0 0 0 0 0 0 0 0 0 0 0 0
2.5327 0.5134 -0.8386 N 0 0 0 0 0 0 0 0 0 0 0 0
3.1603 0.0013 -2.0382 C 0 0 1 0 0 0 0 0 0 0 0 0
4.6059 0.2842 -2.0334 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9985 1.4123 -1.6500 O 0 0 0 0 0 0 0 0 0 0 0 0
5.6129 -0.6553 -2.4334 N 0 0 0 0 0 0 0 0 0 0 0 0
7.0120 -0.3375 -2.3902 C 0 0 1 0 0 0 0 0 0 0 0 0
7.4287 -0.2089 -0.9460 C 0 0 0 0 0 0 0 0 0 0 0 0
6.5160 0.0192 -0.1019 O 0 0 0 0 0 0 0 0 0 0 0 0
8.7591 -0.3277 -0.5206 N 0 0 0 0 0 0 0 0 0 0 0 0
9.1294 -0.1655 0.8731 C 0 0 2 0 0 0 0 0 0 0 0 0
8.2911 -1.1366 1.6942 C 0 0 0 0 0 0 0 0 0 0 0 0
8.9591 1.2588 1.2598 C 0 0 0 0 0 0 0 0 0 0 0 0
10.5549 -0.6144 1.0546 C 0 0 0 0 0 0 0 0 0 0 0 0
10.8987 -1.6287 0.4327 O 0 0 0 0 0 0 0 0 0 0 0 0
11.4540 0.0752 1.8766 N 0 0 0 0 0 0 0 0 0 0 0 0
12.8464 -0.3668 2.0420 C 0 0 1 0 0 0 0 0 0 0 0 0
13.5182 0.5935 2.9765 C 0 0 0 0 0 0 0 0 0 0 0 0
12.7235 -1.7593 2.6727 C 0 0 0 0 0 0 0 0 0 0 0 0
13.5131 -0.5202 0.7436 C 0 0 0 0 0 0 0 0 0 0 0 0
12.8449 -0.2179 -0.3079 O 0 0 0 0 0 0 0 0 0 0 0 0
14.8368 -0.9796 0.5793 N 0 0 0 0 0 0 0 0 0 0 0 0
15.4260 -1.1278 -0.7245 C 0 0 2 0 0 0 0 0 0 0 0 0
15.5854 -2.6123 -1.0720 C 0 0 0 0 0 0 0 0 0 0 0 0
16.7298 -0.4828 -0.9575 C 0 0 1 0 0 0 0 0 0 0 0 0
16.8345 0.9203 -0.8264 N 0 0 2 0 0 0 0 0 0 0 0 0
18.2208 1.2762 -1.1812 C 0 0 0 0 0 0 0 0 0 0 0 0
16.5474 1.5210 0.4253 C 0 0 1 0 0 0 0 0 0 0 0 0
17.5315 1.1974 1.5343 C 0 0 1 0 0 0 0 0 0 0 0 0
17.0641 1.8855 2.6644 O 0 0 0 0 0 0 0 0 0 0 0 0
7.9083 -1.2428 -3.1346 C 0 0 1 0 0 0 0 0 0 0 0 0
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7.5016 -1.2181 -4.6080 C 0 0 2 0 0 0 0 0 0 0 0 0
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2.9135 -1.4600 -2.2393 C 0 0 2 0 0 0 0 0 0 0 0 0
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1.9051 2.7015 1.3820 C 0 0 2 0 0 0 0 0 0 0 0 0
3.2084 2.0573 1.7421 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1947 3.0273 2.7033 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.6352 -1.0361 -0.5650 H 0 0 0 0 0 0 0 0 0 0 0 0
-19.1967 -0.2800 -0.8341 H 0 0 0 0 0 0 0 0 0 0 0 0
-18.0024 0.5185 0.2469 H 0 0 0 0 0 0 0 0 0 0 0 0
-18.4025 0.5946 -2.7147 H 0 0 0 0 0 0 0 0 0 0 0 0
-17.5101 1.8085 -1.7228 H 0 0 0 0 0 0 0 0 0 0 0 0
-16.2275 0.6033 -3.5656 H 0 0 0 0 0 0 0 0 0 0 0 0
-16.5017 -0.9113 -2.7112 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.7709 1.3676 -1.7893 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.2988 -0.1955 -2.4299 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.7817 0.0857 0.2226 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.2922 -1.4429 -0.5483 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.8927 -1.0543 1.1696 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.9400 -1.0542 -0.2867 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.0787 0.5109 1.3425 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.6492 1.1760 1.6935 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.5330 2.5394 -0.3522 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.1060 2.7352 0.6192 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.1656 1.1122 -2.0042 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.3607 3.2157 -1.9872 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.8287 3.9191 -1.2233 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.9721 3.1664 -2.8350 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.9640 -0.1119 -3.4150 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.4675 1.5971 -3.6998 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.9103 0.5410 -5.1203 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.9267 -0.9793 -4.0843 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.7747 1.6958 -3.2061 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.8263 0.1461 -3.4967 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.3695 -1.0070 -1.9667 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.2966 -1.1636 -0.5722 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.0669 -0.5887 1.3232 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.0929 1.1539 2.8202 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.4325 1.3811 1.7151 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.1017 -0.3451 3.3140 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.4953 -0.2123 3.8855 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.5579 -1.8196 3.0100 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.5908 -1.4561 4.5048 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.4972 -2.0387 1.4597 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.1333 -1.5475 0.9085 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.6092 -3.8220 1.7963 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.1168 -3.9570 4.1558 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.6073 -3.7198 1.2113 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.7890 -4.2902 2.8773 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.5588 -0.8363 3.5928 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.0007 -1.4044 4.2811 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.3856 -3.2913 3.9299 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.1115 -3.3151 5.2372 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.4659 -2.0893 5.2604 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7422 1.6885 2.3392 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.0722 3.0134 -0.2429 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7017 4.6765 1.3096 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.8935 3.7476 2.6841 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.8628 4.5653 1.4712 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.2654 3.5313 -0.1319 H 0 0 0 0 0 0 0 0 0 0 0 0
0.6930 0.9582 1.2044 H 0 0 0 0 0 0 0 0 0 0 0 0
2.9141 0.1283 0.0837 H 0 0 0 0 0 0 0 0 0 0 0 0
2.6911 0.5534 -2.8906 H 0 0 0 0 0 0 0 0 0 0 0 0
5.3040 -1.5809 -2.7663 H 0 0 0 0 0 0 0 0 0 0 0 0
7.1220 0.7151 -2.7566 H 0 0 0 0 0 0 0 0 0 0 0 0
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8.4133 -2.1706 1.3862 H 0 0 0 0 0 0 0 0 0 0 0 0
9.1333 1.3596 2.3652 H 0 0 0 0 0 0 0 0 0 0 0 0
9.7532 1.8546 0.7363 H 0 0 0 0 0 0 0 0 0 0 0 0
7.9972 1.7149 1.0372 H 0 0 0 0 0 0 0 0 0 0 0 0
11.1080 0.9244 2.3644 H 0 0 0 0 0 0 0 0 0 0 0 0
13.1760 1.6383 2.8979 H 0 0 0 0 0 0 0 0 0 0 0 0
14.6251 0.4704 2.8268 H 0 0 0 0 0 0 0 0 0 0 0 0
13.3675 0.3045 4.0549 H 0 0 0 0 0 0 0 0 0 0 0 0
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13.2021 -1.6790 3.6833 H 0 0 0 0 0 0 0 0 0 0 0 0
11.6999 -2.1064 2.7803 H 0 0 0 0 0 0 0 0 0 0 0 0
15.3971 -1.2068 1.4079 H 0 0 0 0 0 0 0 0 0 0 0 0
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18.8864 0.7773 -0.4702 H 0 0 0 0 0 0 0 0 0 0 0 0
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18.4211 0.8343 -2.2044 H 0 0 0 0 0 0 0 0 0 0 0 0
16.6788 2.6420 0.2606 H 0 0 0 0 0 0 0 0 0 0 0 0
15.5506 1.4187 0.8349 H 0 0 0 0 0 0 0 0 0 0 0 0
17.5236 0.1233 1.7887 H 0 0 0 0 0 0 0 0 0 0 0 0
18.5443 1.5898 1.3479 H 0 0 0 0 0 0 0 0 0 0 0 0
16.8275 1.2417 3.3928 H 0 0 0 0 0 0 0 0 0 0 0 0
8.9479 -0.8926 -3.1099 H 0 0 0 0 0 0 0 0 0 0 0 0
6.8180 -2.8564 -2.2642 H 0 0 0 0 0 0 0 0 0 0 0 0
8.5254 -2.7889 -1.7219 H 0 0 0 0 0 0 0 0 0 0 0 0
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6.4172 -1.5259 -4.6920 H 0 0 0 0 0 0 0 0 0 0 0 0
8.5887 -1.5748 -6.4416 H 0 0 0 0 0 0 0 0 0 0 0 0
9.3641 -2.2354 -4.9882 H 0 0 0 0 0 0 0 0 0 0 0 0
7.9307 -3.0937 -5.6708 H 0 0 0 0 0 0 0 0 0 0 0 0
3.3560 -1.7988 -3.1830 H 0 0 0 0 0 0 0 0 0 0 0 0
1.2931 -2.7850 -2.6258 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8677 -1.5463 -1.4410 H 0 0 0 0 0 0 0 0 0 0 0 0
1.0025 -1.0985 -3.2252 H 0 0 0 0 0 0 0 0 0 0 0 0
4.1428 -3.0484 -1.4030 H 0 0 0 0 0 0 0 0 0 0 0 0
2.5241 -2.9319 -0.7005 H 0 0 0 0 0 0 0 0 0 0 0 0
3.8074 -1.6455 -0.3057 H 0 0 0 0 0 0 0 0 0 0 0 0
2.0726 3.6467 0.8068 H 0 0 0 0 0 0 0 0 0 0 0 0
3.1046 1.0299 2.1395 H 0 0 0 0 0 0 0 0 0 0 0 0
3.9479 2.0998 0.9461 H 0 0 0 0 0 0 0 0 0 0 0 0
3.5995 2.6664 2.6177 H 0 0 0 0 0 0 0 0 0 0 0 0
0.4172 3.7837 2.5610 H 0 0 0 0 0 0 0 0 0 0 0 0
0.7153 2.0913 3.1031 H 0 0 0 0 0 0 0 0 0 0 0 0
1.9436 3.3899 3.4224 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
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5 6 1 0 0 0 0
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56 57 2 0 0 0 0
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59 61 1 0 0 0 0
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2 86 1 0 0 0 0
2 87 1 0 0 0 0
3 88 1 0 0 0 0
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10102 1 0 0 0 0
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14104 1 0 0 0 0
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15106 1 0 0 0 0
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16109 1 0 0 0 0
17110 1 6 0 0 0
20111 1 0 0 0 0
21112 1 1 0 0 0
22113 1 0 0 0 0
22114 1 0 0 0 0
23115 1 1 0 0 0
24116 1 0 0 0 0
24117 1 0 0 0 0
24118 1 0 0 0 0
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81189 1 0 0 0 0
82190 1 0 0 0 0
82191 1 0 0 0 0
82192 1 0 0 0 0
M END
3D MOL for NP0003268 (Roseoferin C2)
RDKit 3D
192192 0 0 0 0 0 0 0 0999 V2000
-18.0677 -0.0325 -0.7160 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.6174 0.7049 -1.9220 C 0 0 0 0 0 0 0 0 0 0 0 0
-16.3538 0.2039 -2.5091 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.0824 0.2997 -1.7437 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.9745 -0.3673 -0.4534 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.6873 -0.3634 0.2769 C 0 0 0 0 0 0 0 0 0 0 0 0
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3.2084 2.0573 1.7421 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1947 3.0273 2.7033 C 0 0 0 0 0 0 0 0 0 0 0 0
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1.9436 3.3899 3.4224 H 0 0 0 0 0 0 0 0 0 0 0 0
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82191 1 0
82192 1 0
M END
3D SDF for NP0003268 (Roseoferin C2)
Mrv1652307012117083D
192192 0 0 0 0 999 V2000
-18.0677 -0.0325 -0.7160 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.6174 0.7049 -1.9220 C 0 0 1 0 0 0 0 0 0 0 0 0
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-8.9277 0.1207 -4.1330 C 0 0 2 0 0 0 0 0 0 0 0 0
-7.7574 0.5905 -3.2351 C 0 0 2 0 0 0 0 0 0 0 0 0
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1.4794 1.4283 -0.7327 C 0 0 0 0 0 0 0 0 0 0 0 0
0.9681 1.8843 -1.7734 O 0 0 0 0 0 0 0 0 0 0 0 0
2.5327 0.5134 -0.8386 N 0 0 0 0 0 0 0 0 0 0 0 0
3.1603 0.0013 -2.0382 C 0 0 1 0 0 0 0 0 0 0 0 0
4.6059 0.2842 -2.0334 C 0 0 0 0 0 0 0 0 0 0 0 0
4.9985 1.4123 -1.6500 O 0 0 0 0 0 0 0 0 0 0 0 0
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7.0120 -0.3375 -2.3902 C 0 0 1 0 0 0 0 0 0 0 0 0
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6.5160 0.0192 -0.1019 O 0 0 0 0 0 0 0 0 0 0 0 0
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11.4540 0.0752 1.8766 N 0 0 0 0 0 0 0 0 0 0 0 0
12.8464 -0.3668 2.0420 C 0 0 1 0 0 0 0 0 0 0 0 0
13.5182 0.5935 2.9765 C 0 0 0 0 0 0 0 0 0 0 0 0
12.7235 -1.7593 2.6727 C 0 0 0 0 0 0 0 0 0 0 0 0
13.5131 -0.5202 0.7436 C 0 0 0 0 0 0 0 0 0 0 0 0
12.8449 -0.2179 -0.3079 O 0 0 0 0 0 0 0 0 0 0 0 0
14.8368 -0.9796 0.5793 N 0 0 0 0 0 0 0 0 0 0 0 0
15.4260 -1.1278 -0.7245 C 0 0 2 0 0 0 0 0 0 0 0 0
15.5854 -2.6123 -1.0720 C 0 0 0 0 0 0 0 0 0 0 0 0
16.7298 -0.4828 -0.9575 C 0 0 1 0 0 0 0 0 0 0 0 0
16.8345 0.9203 -0.8264 N 0 0 2 0 0 0 0 0 0 0 0 0
18.2208 1.2762 -1.1812 C 0 0 0 0 0 0 0 0 0 0 0 0
16.5474 1.5210 0.4253 C 0 0 1 0 0 0 0 0 0 0 0 0
17.5315 1.1974 1.5343 C 0 0 1 0 0 0 0 0 0 0 0 0
17.0641 1.8855 2.6644 O 0 0 0 0 0 0 0 0 0 0 0 0
7.9083 -1.2428 -3.1346 C 0 0 1 0 0 0 0 0 0 0 0 0
7.8527 -2.6740 -2.6204 C 0 0 0 0 0 0 0 0 0 0 0 0
7.5016 -1.2181 -4.6080 C 0 0 2 0 0 0 0 0 0 0 0 0
8.3681 -2.1068 -5.4681 C 0 0 0 0 0 0 0 0 0 0 0 0
2.9135 -1.4600 -2.2393 C 0 0 2 0 0 0 0 0 0 0 0 0
1.3919 -1.7064 -2.3810 C 0 0 0 0 0 0 0 0 0 0 0 0
3.3652 -2.3095 -1.0744 C 0 0 0 0 0 0 0 0 0 0 0 0
1.9051 2.7015 1.3820 C 0 0 2 0 0 0 0 0 0 0 0 0
3.2084 2.0573 1.7421 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1947 3.0273 2.7033 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.6352 -1.0361 -0.5650 H 0 0 0 0 0 0 0 0 0 0 0 0
-19.1967 -0.2800 -0.8341 H 0 0 0 0 0 0 0 0 0 0 0 0
-18.0024 0.5185 0.2469 H 0 0 0 0 0 0 0 0 0 0 0 0
-18.4025 0.5946 -2.7147 H 0 0 0 0 0 0 0 0 0 0 0 0
-17.5101 1.8085 -1.7228 H 0 0 0 0 0 0 0 0 0 0 0 0
-16.2275 0.6033 -3.5656 H 0 0 0 0 0 0 0 0 0 0 0 0
-16.5017 -0.9113 -2.7112 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.7709 1.3676 -1.7893 H 0 0 0 0 0 0 0 0 0 0 0 0
-14.2988 -0.1955 -2.4299 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.7817 0.0857 0.2226 H 0 0 0 0 0 0 0 0 0 0 0 0
-15.2922 -1.4429 -0.5483 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.8927 -1.0543 1.1696 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.9400 -1.0542 -0.2867 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.0787 0.5109 1.3425 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.6492 1.1760 1.6935 H 0 0 0 0 0 0 0 0 0 0 0 0
-13.5330 2.5394 -0.3522 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.1060 2.7352 0.6192 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.1656 1.1122 -2.0042 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.3607 3.2157 -1.9872 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.8287 3.9191 -1.2233 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.9721 3.1664 -2.8350 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.9640 -0.1119 -3.4150 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.4675 1.5971 -3.6998 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.9103 0.5410 -5.1203 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.9267 -0.9793 -4.0843 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.7747 1.6958 -3.2061 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.8263 0.1461 -3.4967 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.3695 -1.0070 -1.9667 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.2966 -1.1636 -0.5722 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.0669 -0.5887 1.3232 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.0929 1.1539 2.8202 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.4325 1.3811 1.7151 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.1017 -0.3451 3.3140 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.4953 -0.2123 3.8855 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.5579 -1.8196 3.0100 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.5908 -1.4561 4.5048 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.4972 -2.0387 1.4597 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.1333 -1.5475 0.9085 H 0 0 0 0 0 0 0 0 0 0 0 0
-7.6092 -3.8220 1.7963 H 0 0 0 0 0 0 0 0 0 0 0 0
-8.1168 -3.9570 4.1558 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.6073 -3.7198 1.2113 H 0 0 0 0 0 0 0 0 0 0 0 0
-9.7890 -4.2902 2.8773 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.5588 -0.8363 3.5928 H 0 0 0 0 0 0 0 0 0 0 0 0
-10.0007 -1.4044 4.2811 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.3856 -3.2913 3.9299 H 0 0 0 0 0 0 0 0 0 0 0 0
-11.1115 -3.3151 5.2372 H 0 0 0 0 0 0 0 0 0 0 0 0
-12.4659 -2.0893 5.2604 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7422 1.6885 2.3392 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.0722 3.0134 -0.2429 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.7017 4.6765 1.3096 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.8935 3.7476 2.6841 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.8628 4.5653 1.4712 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.2654 3.5313 -0.1319 H 0 0 0 0 0 0 0 0 0 0 0 0
0.6930 0.9582 1.2044 H 0 0 0 0 0 0 0 0 0 0 0 0
2.9141 0.1283 0.0837 H 0 0 0 0 0 0 0 0 0 0 0 0
2.6911 0.5534 -2.8906 H 0 0 0 0 0 0 0 0 0 0 0 0
5.3040 -1.5809 -2.7663 H 0 0 0 0 0 0 0 0 0 0 0 0
7.1220 0.7151 -2.7566 H 0 0 0 0 0 0 0 0 0 0 0 0
9.5271 -0.5334 -1.2151 H 0 0 0 0 0 0 0 0 0 0 0 0
8.7449 -1.0857 2.7390 H 0 0 0 0 0 0 0 0 0 0 0 0
7.2568 -0.7950 1.8530 H 0 0 0 0 0 0 0 0 0 0 0 0
8.4133 -2.1706 1.3862 H 0 0 0 0 0 0 0 0 0 0 0 0
9.1333 1.3596 2.3652 H 0 0 0 0 0 0 0 0 0 0 0 0
9.7532 1.8546 0.7363 H 0 0 0 0 0 0 0 0 0 0 0 0
7.9972 1.7149 1.0372 H 0 0 0 0 0 0 0 0 0 0 0 0
11.1080 0.9244 2.3644 H 0 0 0 0 0 0 0 0 0 0 0 0
13.1760 1.6383 2.8979 H 0 0 0 0 0 0 0 0 0 0 0 0
14.6251 0.4704 2.8268 H 0 0 0 0 0 0 0 0 0 0 0 0
13.3675 0.3045 4.0549 H 0 0 0 0 0 0 0 0 0 0 0 0
13.3759 -2.4511 2.0977 H 0 0 0 0 0 0 0 0 0 0 0 0
13.2021 -1.6790 3.6833 H 0 0 0 0 0 0 0 0 0 0 0 0
11.6999 -2.1064 2.7803 H 0 0 0 0 0 0 0 0 0 0 0 0
15.3971 -1.2068 1.4079 H 0 0 0 0 0 0 0 0 0 0 0 0
14.6622 -0.7749 -1.4758 H 0 0 0 0 0 0 0 0 0 0 0 0
16.5858 -2.8785 -0.6705 H 0 0 0 0 0 0 0 0 0 0 0 0
14.8423 -3.2450 -0.5841 H 0 0 0 0 0 0 0 0 0 0 0 0
15.5913 -2.7871 -2.1462 H 0 0 0 0 0 0 0 0 0 0 0 0
17.5612 -0.9965 -0.3729 H 0 0 0 0 0 0 0 0 0 0 0 0
17.0366 -0.7119 -2.0305 H 0 0 0 0 0 0 0 0 0 0 0 0
18.8864 0.7773 -0.4702 H 0 0 0 0 0 0 0 0 0 0 0 0
18.3105 2.3683 -1.2616 H 0 0 0 0 0 0 0 0 0 0 0 0
18.4211 0.8343 -2.2044 H 0 0 0 0 0 0 0 0 0 0 0 0
16.6788 2.6420 0.2606 H 0 0 0 0 0 0 0 0 0 0 0 0
15.5506 1.4187 0.8349 H 0 0 0 0 0 0 0 0 0 0 0 0
17.5236 0.1233 1.7887 H 0 0 0 0 0 0 0 0 0 0 0 0
18.5443 1.5898 1.3479 H 0 0 0 0 0 0 0 0 0 0 0 0
16.8275 1.2417 3.3928 H 0 0 0 0 0 0 0 0 0 0 0 0
8.9479 -0.8926 -3.1099 H 0 0 0 0 0 0 0 0 0 0 0 0
6.8180 -2.8564 -2.2642 H 0 0 0 0 0 0 0 0 0 0 0 0
8.5254 -2.7889 -1.7219 H 0 0 0 0 0 0 0 0 0 0 0 0
8.0785 -3.3657 -3.4232 H 0 0 0 0 0 0 0 0 0 0 0 0
7.5626 -0.1837 -4.9721 H 0 0 0 0 0 0 0 0 0 0 0 0
6.4172 -1.5259 -4.6920 H 0 0 0 0 0 0 0 0 0 0 0 0
8.5887 -1.5748 -6.4416 H 0 0 0 0 0 0 0 0 0 0 0 0
9.3641 -2.2354 -4.9882 H 0 0 0 0 0 0 0 0 0 0 0 0
7.9307 -3.0937 -5.6708 H 0 0 0 0 0 0 0 0 0 0 0 0
3.3560 -1.7988 -3.1830 H 0 0 0 0 0 0 0 0 0 0 0 0
1.2931 -2.7850 -2.6258 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8677 -1.5463 -1.4410 H 0 0 0 0 0 0 0 0 0 0 0 0
1.0025 -1.0985 -3.2252 H 0 0 0 0 0 0 0 0 0 0 0 0
4.1428 -3.0484 -1.4030 H 0 0 0 0 0 0 0 0 0 0 0 0
2.5241 -2.9319 -0.7005 H 0 0 0 0 0 0 0 0 0 0 0 0
3.8074 -1.6455 -0.3057 H 0 0 0 0 0 0 0 0 0 0 0 0
2.0726 3.6467 0.8068 H 0 0 0 0 0 0 0 0 0 0 0 0
3.1046 1.0299 2.1395 H 0 0 0 0 0 0 0 0 0 0 0 0
3.9479 2.0998 0.9461 H 0 0 0 0 0 0 0 0 0 0 0 0
3.5995 2.6664 2.6177 H 0 0 0 0 0 0 0 0 0 0 0 0
0.4172 3.7837 2.5610 H 0 0 0 0 0 0 0 0 0 0 0 0
0.7153 2.0913 3.1031 H 0 0 0 0 0 0 0 0 0 0 0 0
1.9436 3.3899 3.4224 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
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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
42 43 2 0 0 0 0
42 44 1 0 0 0 0
44 45 1 0 0 0 0
45 46 1 0 0 0 0
46 47 2 0 0 0 0
46 48 1 0 0 0 0
48 49 1 0 0 0 0
49 50 1 0 0 0 0
50 51 2 0 0 0 0
50 52 1 0 0 0 0
52 53 1 0 0 0 0
53 54 1 0 0 0 0
53 55 1 0 0 0 0
53 56 1 6 0 0 0
56 57 2 0 0 0 0
56 58 1 0 0 0 0
58 59 1 0 0 0 0
59 60 1 0 0 0 0
59 61 1 0 0 0 0
59 62 1 6 0 0 0
62 63 2 0 0 0 0
62 64 1 0 0 0 0
64 65 1 0 0 0 0
65 66 1 0 0 0 0
65 67 1 0 0 0 0
67 68 1 0 0 0 0
68 69 1 0 0 0 0
68 70 1 0 0 0 0
70 71 1 0 0 0 0
71 72 1 0 0 0 0
49 73 1 0 0 0 0
73 74 1 0 0 0 0
73 75 1 0 0 0 0
75 76 1 0 0 0 0
45 77 1 0 0 0 0
77 78 1 0 0 0 0
77 79 1 0 0 0 0
41 80 1 0 0 0 0
80 81 1 0 0 0 0
80 82 1 0 0 0 0
17 13 1 0 0 0 0
1 83 1 0 0 0 0
1 84 1 0 0 0 0
1 85 1 0 0 0 0
2 86 1 0 0 0 0
2 87 1 0 0 0 0
3 88 1 0 0 0 0
3 89 1 0 0 0 0
4 90 1 0 0 0 0
4 91 1 0 0 0 0
5 92 1 0 0 0 0
5 93 1 0 0 0 0
6 94 1 0 0 0 0
6 95 1 0 0 0 0
7 96 1 0 0 0 0
7 97 1 0 0 0 0
8 98 1 0 0 0 0
8 99 1 0 0 0 0
9100 1 6 0 0 0
10101 1 0 0 0 0
10102 1 0 0 0 0
10103 1 0 0 0 0
14104 1 0 0 0 0
14105 1 0 0 0 0
15106 1 0 0 0 0
15107 1 0 0 0 0
16108 1 0 0 0 0
16109 1 0 0 0 0
17110 1 6 0 0 0
20111 1 0 0 0 0
21112 1 1 0 0 0
22113 1 0 0 0 0
22114 1 0 0 0 0
23115 1 1 0 0 0
24116 1 0 0 0 0
24117 1 0 0 0 0
24118 1 0 0 0 0
25119 1 0 0 0 0
25120 1 0 0 0 0
26121 1 6 0 0 0
27122 1 0 0 0 0
28123 1 0 0 0 0
28124 1 0 0 0 0
31125 1 0 0 0 0
31126 1 0 0 0 0
32127 1 0 0 0 0
32128 1 0 0 0 0
32129 1 0 0 0 0
35130 1 0 0 0 0
36131 1 6 0 0 0
37132 1 0 0 0 0
37133 1 0 0 0 0
37134 1 0 0 0 0
40135 1 0 0 0 0
41136 1 1 0 0 0
44137 1 0 0 0 0
45138 1 6 0 0 0
48139 1 0 0 0 0
49140 1 6 0 0 0
52141 1 0 0 0 0
54142 1 0 0 0 0
54143 1 0 0 0 0
54144 1 0 0 0 0
55145 1 0 0 0 0
55146 1 0 0 0 0
55147 1 0 0 0 0
58148 1 0 0 0 0
60149 1 0 0 0 0
60150 1 0 0 0 0
60151 1 0 0 0 0
61152 1 0 0 0 0
61153 1 0 0 0 0
61154 1 0 0 0 0
64155 1 0 0 0 0
65156 1 6 0 0 0
66157 1 0 0 0 0
66158 1 0 0 0 0
66159 1 0 0 0 0
67160 1 0 0 0 0
67161 1 0 0 0 0
69162 1 0 0 0 0
69163 1 0 0 0 0
69164 1 0 0 0 0
70165 1 0 0 0 0
70166 1 0 0 0 0
71167 1 0 0 0 0
71168 1 0 0 0 0
72169 1 0 0 0 0
73170 1 6 0 0 0
74171 1 0 0 0 0
74172 1 0 0 0 0
74173 1 0 0 0 0
75174 1 0 0 0 0
75175 1 0 0 0 0
76176 1 0 0 0 0
76177 1 0 0 0 0
76178 1 0 0 0 0
77179 1 6 0 0 0
78180 1 0 0 0 0
78181 1 0 0 0 0
78182 1 0 0 0 0
79183 1 0 0 0 0
79184 1 0 0 0 0
79185 1 0 0 0 0
80186 1 6 0 0 0
81187 1 0 0 0 0
81188 1 0 0 0 0
81189 1 0 0 0 0
82190 1 0 0 0 0
82191 1 0 0 0 0
82192 1 0 0 0 0
M END
> <DATABASE_ID>
NP0003268
> <DATABASE_NAME>
NP-MRD
> <SMILES>
[H]OC([H])([H])C([H])([H])N(C([H])([H])[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@]([H])(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])(C([H])([H])[H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])[C@@]([H])(C([H])([H])[H])C([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/C60H110N10O12/c1-18-21-22-23-24-25-27-40(10)56(80)70-29-26-28-46(70)52(76)63-45(33-38(8)32-44(73)34-43(72)20-3)51(75)62-42(12)50(74)64-47(36(4)5)53(77)65-48(37(6)7)54(78)66-49(39(9)19-2)55(79)67-60(15,16)58(82)68-59(13,14)57(81)61-41(11)35-69(17)30-31-71/h36-42,44-49,71,73H,18-35H2,1-17H3,(H,61,81)(H,62,75)(H,63,76)(H,64,74)(H,65,77)(H,66,78)(H,67,79)(H,68,82)/t38-,39+,40-,41-,42+,44-,45-,46+,47-,48-,49-/m1/s1
> <INCHI_KEY>
DEGMKTXWWRMWKD-UHFFFAOYSA-N
> <FORMULA>
C60H110N10O12
> <MOLECULAR_WEIGHT>
1163.598
> <EXACT_MASS>
1162.830469022
> <JCHEM_ACCEPTOR_COUNT>
13
> <JCHEM_ATOM_COUNT>
192
> <JCHEM_AVERAGE_POLARIZABILITY>
133.9703534461033
> <JCHEM_BIOAVAILABILITY>
0
> <JCHEM_DONOR_COUNT>
10
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
0
> <JCHEM_IUPAC>
(2R,4S)-6-hydroxy-N-[(1S)-1-{[(1R)-1-{[(1R)-1-{[(1R,2S)-1-({1-[(1-{[(2R)-1-[(2-hydroxyethyl)(methyl)amino]propan-2-yl]carbamoyl}-1-methylethyl)carbamoyl]-1-methylethyl}carbamoyl)-2-methylbutyl]carbamoyl}-2-methylpropyl]carbamoyl}-2-methylpropyl]carbamoyl}ethyl]-4-methyl-2-{[(2S)-1-[(2R)-2-methyldecanoyl]pyrrolidin-2-yl]formamido}-8-oxodecanamide
> <ALOGPS_LOGP>
4.22
> <JCHEM_LOGP>
4.314032441999997
> <ALOGPS_LOGS>
-5.06
> <JCHEM_MDDR_LIKE_RULE>
0
> <JCHEM_NUMBER_OF_RINGS>
1
> <JCHEM_PHYSIOLOGICAL_CHARGE>
1
> <JCHEM_PKA>
12.006876609812357
> <JCHEM_PKA_STRONGEST_ACIDIC>
11.617939804206891
> <JCHEM_PKA_STRONGEST_BASIC>
8.453896747207695
> <JCHEM_POLAR_SURFACE_AREA>
313.87999999999994
> <JCHEM_REFRACTIVITY>
315.4194
> <JCHEM_ROTATABLE_BOND_COUNT>
39
> <JCHEM_RULE_OF_FIVE>
0
> <ALOGPS_SOLUBILITY>
1.02e-02 g/l
> <JCHEM_TRADITIONAL_IUPAC>
(2R,4S)-6-hydroxy-N-[(1S)-1-{[(1R)-1-{[(1R)-1-{[(1R,2S)-1-({1-[(1-{[(2R)-1-[(2-hydroxyethyl)(methyl)amino]propan-2-yl]carbamoyl}-1-methylethyl)carbamoyl]-1-methylethyl}carbamoyl)-2-methylbutyl]carbamoyl}-2-methylpropyl]carbamoyl}-2-methylpropyl]carbamoyl}ethyl]-4-methyl-2-{[(2S)-1-[(2R)-2-methyldecanoyl]pyrrolidin-2-yl]formamido}-8-oxodecanamide
> <JCHEM_VEBER_RULE>
0
$$$$
3D-SDF for NP0003268 (Roseoferin C2)
RDKit 3D
192192 0 0 0 0 0 0 0 0999 V2000
-18.0677 -0.0325 -0.7160 C 0 0 0 0 0 0 0 0 0 0 0 0
-17.6174 0.7049 -1.9220 C 0 0 0 0 0 0 0 0 0 0 0 0
-16.3538 0.2039 -2.5091 C 0 0 0 0 0 0 0 0 0 0 0 0
-15.0824 0.2997 -1.7437 C 0 0 0 0 0 0 0 0 0 0 0 0
-14.9745 -0.3673 -0.4534 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.6873 -0.3634 0.2769 C 0 0 0 0 0 0 0 0 0 0 0 0
-13.0435 0.8231 0.7883 C 0 0 0 0 0 0 0 0 0 0 0 0
-12.6436 1.9592 -0.0386 C 0 0 0 0 0 0 0 0 0 0 0 0
-11.7538 1.7422 -1.1832 C 0 0 1 0 0 0 0 0 0 0 0 0
-11.4475 3.0887 -1.8712 C 0 0 0 0 0 0 0 0 0 0 0 0
-10.4398 1.1269 -0.8777 C 0 0 0 0 0 0 0 0 0 0 0 0
-9.9984 1.0283 0.2915 O 0 0 0 0 0 0 0 0 0 0 0 0
-9.6513 0.6279 -1.9583 N 0 0 0 0 0 0 0 0 0 0 0 0
-10.1222 0.6325 -3.3339 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.9277 0.1207 -4.1330 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.7574 0.5905 -3.2351 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.3490 0.0749 -1.9032 C 0 0 1 0 0 0 0 0 0 0 0 0
-7.4852 0.5687 -0.7870 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.6946 1.7203 -0.4029 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.4845 -0.2568 -0.1988 N 0 0 0 0 0 0 0 0 0 0 0 0
-5.7295 0.3063 0.9332 C 0 0 2 0 0 0 0 0 0 0 0 0
-6.6976 0.6350 1.9924 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.3042 -0.5595 2.7087 C 0 0 2 0 0 0 0 0 0 0 0 0
-6.0951 -1.0990 3.5901 C 0 0 0 0 0 0 0 0 0 0 0 0
-7.5497 -1.7708 1.7833 C 0 0 0 0 0 0 0 0 0 0 0 0
-8.1552 -2.9014 2.5132 C 0 0 1 0 0 0 0 0 0 0 0 0
-7.4943 -3.3380 3.6657 O 0 0 0 0 0 0 0 0 0 0 0 0
-9.5282 -3.3380 2.2948 C 0 0 0 0 0 0 0 0 0 0 0 0
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M END
PDB for NP0003268 (Roseoferin C2)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 -18.068 -0.033 -0.716 0.00 0.00 C+0 HETATM 2 C UNK 0 -17.617 0.705 -1.922 0.00 0.00 C+0 HETATM 3 C UNK 0 -16.354 0.204 -2.509 0.00 0.00 C+0 HETATM 4 C UNK 0 -15.082 0.300 -1.744 0.00 0.00 C+0 HETATM 5 C UNK 0 -14.975 -0.367 -0.453 0.00 0.00 C+0 HETATM 6 C UNK 0 -13.687 -0.363 0.277 0.00 0.00 C+0 HETATM 7 C UNK 0 -13.043 0.823 0.788 0.00 0.00 C+0 HETATM 8 C UNK 0 -12.644 1.959 -0.039 0.00 0.00 C+0 HETATM 9 C UNK 0 -11.754 1.742 -1.183 0.00 0.00 C+0 HETATM 10 C UNK 0 -11.447 3.089 -1.871 0.00 0.00 C+0 HETATM 11 C UNK 0 -10.440 1.127 -0.878 0.00 0.00 C+0 HETATM 12 O UNK 0 -9.998 1.028 0.292 0.00 0.00 O+0 HETATM 13 N UNK 0 -9.651 0.628 -1.958 0.00 0.00 N+0 HETATM 14 C UNK 0 -10.122 0.633 -3.334 0.00 0.00 C+0 HETATM 15 C UNK 0 -8.928 0.121 -4.133 0.00 0.00 C+0 HETATM 16 C UNK 0 -7.757 0.591 -3.235 0.00 0.00 C+0 HETATM 17 C UNK 0 -8.349 0.075 -1.903 0.00 0.00 C+0 HETATM 18 C UNK 0 -7.485 0.569 -0.787 0.00 0.00 C+0 HETATM 19 O UNK 0 -7.695 1.720 -0.403 0.00 0.00 O+0 HETATM 20 N UNK 0 -6.484 -0.257 -0.199 0.00 0.00 N+0 HETATM 21 C UNK 0 -5.729 0.306 0.933 0.00 0.00 C+0 HETATM 22 C UNK 0 -6.698 0.635 1.992 0.00 0.00 C+0 HETATM 23 C UNK 0 -7.304 -0.560 2.709 0.00 0.00 C+0 HETATM 24 C UNK 0 -6.095 -1.099 3.590 0.00 0.00 C+0 HETATM 25 C UNK 0 -7.550 -1.771 1.783 0.00 0.00 C+0 HETATM 26 C UNK 0 -8.155 -2.901 2.513 0.00 0.00 C+0 HETATM 27 O UNK 0 -7.494 -3.338 3.666 0.00 0.00 O+0 HETATM 28 C UNK 0 -9.528 -3.338 2.295 0.00 0.00 C+0 HETATM 29 C UNK 0 -10.633 -2.385 2.444 0.00 0.00 C+0 HETATM 30 O UNK 0 -11.344 -2.090 1.532 0.00 0.00 O+0 HETATM 31 C UNK 0 -10.907 -1.736 3.792 0.00 0.00 C+0 HETATM 32 C UNK 0 -11.774 -2.665 4.626 0.00 0.00 C+0 HETATM 33 C UNK 0 -4.772 1.271 0.498 0.00 0.00 C+0 HETATM 34 O UNK 0 -4.739 1.654 -0.741 0.00 0.00 O+0 HETATM 35 N UNK 0 -3.800 1.866 1.327 0.00 0.00 N+0 HETATM 36 C UNK 0 -2.789 2.797 0.783 0.00 0.00 C+0 HETATM 37 C UNK 0 -2.833 4.063 1.617 0.00 0.00 C+0 HETATM 38 C UNK 0 -1.467 2.103 0.901 0.00 0.00 C+0 HETATM 39 O UNK 0 -1.416 1.004 1.489 0.00 0.00 O+0 HETATM 40 N UNK 0 -0.267 2.647 0.371 0.00 0.00 N+0 HETATM 41 C UNK 0 0.966 1.855 0.585 0.00 0.00 C+0 HETATM 42 C UNK 0 1.479 1.428 -0.733 0.00 0.00 C+0 HETATM 43 O UNK 0 0.968 1.884 -1.773 0.00 0.00 O+0 HETATM 44 N UNK 0 2.533 0.513 -0.839 0.00 0.00 N+0 HETATM 45 C UNK 0 3.160 0.001 -2.038 0.00 0.00 C+0 HETATM 46 C UNK 0 4.606 0.284 -2.033 0.00 0.00 C+0 HETATM 47 O UNK 0 4.999 1.412 -1.650 0.00 0.00 O+0 HETATM 48 N UNK 0 5.613 -0.655 -2.433 0.00 0.00 N+0 HETATM 49 C UNK 0 7.012 -0.338 -2.390 0.00 0.00 C+0 HETATM 50 C UNK 0 7.429 -0.209 -0.946 0.00 0.00 C+0 HETATM 51 O UNK 0 6.516 0.019 -0.102 0.00 0.00 O+0 HETATM 52 N UNK 0 8.759 -0.328 -0.521 0.00 0.00 N+0 HETATM 53 C UNK 0 9.129 -0.166 0.873 0.00 0.00 C+0 HETATM 54 C UNK 0 8.291 -1.137 1.694 0.00 0.00 C+0 HETATM 55 C UNK 0 8.959 1.259 1.260 0.00 0.00 C+0 HETATM 56 C UNK 0 10.555 -0.614 1.055 0.00 0.00 C+0 HETATM 57 O UNK 0 10.899 -1.629 0.433 0.00 0.00 O+0 HETATM 58 N UNK 0 11.454 0.075 1.877 0.00 0.00 N+0 HETATM 59 C UNK 0 12.846 -0.367 2.042 0.00 0.00 C+0 HETATM 60 C UNK 0 13.518 0.594 2.977 0.00 0.00 C+0 HETATM 61 C UNK 0 12.723 -1.759 2.673 0.00 0.00 C+0 HETATM 62 C UNK 0 13.513 -0.520 0.744 0.00 0.00 C+0 HETATM 63 O UNK 0 12.845 -0.218 -0.308 0.00 0.00 O+0 HETATM 64 N UNK 0 14.837 -0.980 0.579 0.00 0.00 N+0 HETATM 65 C UNK 0 15.426 -1.128 -0.725 0.00 0.00 C+0 HETATM 66 C UNK 0 15.585 -2.612 -1.072 0.00 0.00 C+0 HETATM 67 C UNK 0 16.730 -0.483 -0.958 0.00 0.00 C+0 HETATM 68 N UNK 0 16.834 0.920 -0.826 0.00 0.00 N+0 HETATM 69 C UNK 0 18.221 1.276 -1.181 0.00 0.00 C+0 HETATM 70 C UNK 0 16.547 1.521 0.425 0.00 0.00 C+0 HETATM 71 C UNK 0 17.532 1.197 1.534 0.00 0.00 C+0 HETATM 72 O UNK 0 17.064 1.886 2.664 0.00 0.00 O+0 HETATM 73 C UNK 0 7.908 -1.243 -3.135 0.00 0.00 C+0 HETATM 74 C UNK 0 7.853 -2.674 -2.620 0.00 0.00 C+0 HETATM 75 C UNK 0 7.502 -1.218 -4.608 0.00 0.00 C+0 HETATM 76 C UNK 0 8.368 -2.107 -5.468 0.00 0.00 C+0 HETATM 77 C UNK 0 2.914 -1.460 -2.239 0.00 0.00 C+0 HETATM 78 C UNK 0 1.392 -1.706 -2.381 0.00 0.00 C+0 HETATM 79 C UNK 0 3.365 -2.309 -1.074 0.00 0.00 C+0 HETATM 80 C UNK 0 1.905 2.701 1.382 0.00 0.00 C+0 HETATM 81 C UNK 0 3.208 2.057 1.742 0.00 0.00 C+0 HETATM 82 C UNK 0 1.195 3.027 2.703 0.00 0.00 C+0 HETATM 83 H UNK 0 -17.635 -1.036 -0.565 0.00 0.00 H+0 HETATM 84 H UNK 0 -19.197 -0.280 -0.834 0.00 0.00 H+0 HETATM 85 H UNK 0 -18.002 0.519 0.247 0.00 0.00 H+0 HETATM 86 H UNK 0 -18.402 0.595 -2.715 0.00 0.00 H+0 HETATM 87 H UNK 0 -17.510 1.809 -1.723 0.00 0.00 H+0 HETATM 88 H UNK 0 -16.227 0.603 -3.566 0.00 0.00 H+0 HETATM 89 H UNK 0 -16.502 -0.911 -2.711 0.00 0.00 H+0 HETATM 90 H UNK 0 -14.771 1.368 -1.789 0.00 0.00 H+0 HETATM 91 H UNK 0 -14.299 -0.196 -2.430 0.00 0.00 H+0 HETATM 92 H UNK 0 -15.782 0.086 0.223 0.00 0.00 H+0 HETATM 93 H UNK 0 -15.292 -1.443 -0.548 0.00 0.00 H+0 HETATM 94 H UNK 0 -13.893 -1.054 1.170 0.00 0.00 H+0 HETATM 95 H UNK 0 -12.940 -1.054 -0.287 0.00 0.00 H+0 HETATM 96 H UNK 0 -12.079 0.511 1.343 0.00 0.00 H+0 HETATM 97 H UNK 0 -13.649 1.176 1.694 0.00 0.00 H+0 HETATM 98 H UNK 0 -13.533 2.539 -0.352 0.00 0.00 H+0 HETATM 99 H UNK 0 -12.106 2.735 0.619 0.00 0.00 H+0 HETATM 100 H UNK 0 -12.166 1.112 -2.004 0.00 0.00 H+0 HETATM 101 H UNK 0 -10.361 3.216 -1.987 0.00 0.00 H+0 HETATM 102 H UNK 0 -11.829 3.919 -1.223 0.00 0.00 H+0 HETATM 103 H UNK 0 -11.972 3.166 -2.835 0.00 0.00 H+0 HETATM 104 H UNK 0 -10.964 -0.112 -3.415 0.00 0.00 H+0 HETATM 105 H UNK 0 -10.467 1.597 -3.700 0.00 0.00 H+0 HETATM 106 H UNK 0 -8.910 0.541 -5.120 0.00 0.00 H+0 HETATM 107 H UNK 0 -8.927 -0.979 -4.084 0.00 0.00 H+0 HETATM 108 H UNK 0 -7.775 1.696 -3.206 0.00 0.00 H+0 HETATM 109 H UNK 0 -6.826 0.146 -3.497 0.00 0.00 H+0 HETATM 110 H UNK 0 -8.370 -1.007 -1.967 0.00 0.00 H+0 HETATM 111 H UNK 0 -6.297 -1.164 -0.572 0.00 0.00 H+0 HETATM 112 H UNK 0 -5.067 -0.589 1.323 0.00 0.00 H+0 HETATM 113 H UNK 0 -6.093 1.154 2.820 0.00 0.00 H+0 HETATM 114 H UNK 0 -7.433 1.381 1.715 0.00 0.00 H+0 HETATM 115 H UNK 0 -8.102 -0.345 3.314 0.00 0.00 H+0 HETATM 116 H UNK 0 -5.495 -0.212 3.886 0.00 0.00 H+0 HETATM 117 H UNK 0 -5.558 -1.820 3.010 0.00 0.00 H+0 HETATM 118 H UNK 0 -6.591 -1.456 4.505 0.00 0.00 H+0 HETATM 119 H UNK 0 -6.497 -2.039 1.460 0.00 0.00 H+0 HETATM 120 H UNK 0 -8.133 -1.548 0.909 0.00 0.00 H+0 HETATM 121 H UNK 0 -7.609 -3.822 1.796 0.00 0.00 H+0 HETATM 122 H UNK 0 -8.117 -3.957 4.156 0.00 0.00 H+0 HETATM 123 H UNK 0 -9.607 -3.720 1.211 0.00 0.00 H+0 HETATM 124 H UNK 0 -9.789 -4.290 2.877 0.00 0.00 H+0 HETATM 125 H UNK 0 -11.559 -0.836 3.593 0.00 0.00 H+0 HETATM 126 H UNK 0 -10.001 -1.404 4.281 0.00 0.00 H+0 HETATM 127 H UNK 0 -12.386 -3.291 3.930 0.00 0.00 H+0 HETATM 128 H UNK 0 -11.111 -3.315 5.237 0.00 0.00 H+0 HETATM 129 H UNK 0 -12.466 -2.089 5.260 0.00 0.00 H+0 HETATM 130 H UNK 0 -3.742 1.688 2.339 0.00 0.00 H+0 HETATM 131 H UNK 0 -3.072 3.013 -0.243 0.00 0.00 H+0 HETATM 132 H UNK 0 -3.702 4.676 1.310 0.00 0.00 H+0 HETATM 133 H UNK 0 -2.894 3.748 2.684 0.00 0.00 H+0 HETATM 134 H UNK 0 -1.863 4.565 1.471 0.00 0.00 H+0 HETATM 135 H UNK 0 -0.265 3.531 -0.132 0.00 0.00 H+0 HETATM 136 H UNK 0 0.693 0.958 1.204 0.00 0.00 H+0 HETATM 137 H UNK 0 2.914 0.128 0.084 0.00 0.00 H+0 HETATM 138 H UNK 0 2.691 0.553 -2.891 0.00 0.00 H+0 HETATM 139 H UNK 0 5.304 -1.581 -2.766 0.00 0.00 H+0 HETATM 140 H UNK 0 7.122 0.715 -2.757 0.00 0.00 H+0 HETATM 141 H UNK 0 9.527 -0.533 -1.215 0.00 0.00 H+0 HETATM 142 H UNK 0 8.745 -1.086 2.739 0.00 0.00 H+0 HETATM 143 H UNK 0 7.257 -0.795 1.853 0.00 0.00 H+0 HETATM 144 H UNK 0 8.413 -2.171 1.386 0.00 0.00 H+0 HETATM 145 H UNK 0 9.133 1.360 2.365 0.00 0.00 H+0 HETATM 146 H UNK 0 9.753 1.855 0.736 0.00 0.00 H+0 HETATM 147 H UNK 0 7.997 1.715 1.037 0.00 0.00 H+0 HETATM 148 H UNK 0 11.108 0.924 2.364 0.00 0.00 H+0 HETATM 149 H UNK 0 13.176 1.638 2.898 0.00 0.00 H+0 HETATM 150 H UNK 0 14.625 0.470 2.827 0.00 0.00 H+0 HETATM 151 H UNK 0 13.367 0.305 4.055 0.00 0.00 H+0 HETATM 152 H UNK 0 13.376 -2.451 2.098 0.00 0.00 H+0 HETATM 153 H UNK 0 13.202 -1.679 3.683 0.00 0.00 H+0 HETATM 154 H UNK 0 11.700 -2.106 2.780 0.00 0.00 H+0 HETATM 155 H UNK 0 15.397 -1.207 1.408 0.00 0.00 H+0 HETATM 156 H UNK 0 14.662 -0.775 -1.476 0.00 0.00 H+0 HETATM 157 H UNK 0 16.586 -2.878 -0.671 0.00 0.00 H+0 HETATM 158 H UNK 0 14.842 -3.245 -0.584 0.00 0.00 H+0 HETATM 159 H UNK 0 15.591 -2.787 -2.146 0.00 0.00 H+0 HETATM 160 H UNK 0 17.561 -0.997 -0.373 0.00 0.00 H+0 HETATM 161 H UNK 0 17.037 -0.712 -2.030 0.00 0.00 H+0 HETATM 162 H UNK 0 18.886 0.777 -0.470 0.00 0.00 H+0 HETATM 163 H UNK 0 18.311 2.368 -1.262 0.00 0.00 H+0 HETATM 164 H UNK 0 18.421 0.834 -2.204 0.00 0.00 H+0 HETATM 165 H UNK 0 16.679 2.642 0.261 0.00 0.00 H+0 HETATM 166 H UNK 0 15.551 1.419 0.835 0.00 0.00 H+0 HETATM 167 H UNK 0 17.524 0.123 1.789 0.00 0.00 H+0 HETATM 168 H UNK 0 18.544 1.590 1.348 0.00 0.00 H+0 HETATM 169 H UNK 0 16.828 1.242 3.393 0.00 0.00 H+0 HETATM 170 H UNK 0 8.948 -0.893 -3.110 0.00 0.00 H+0 HETATM 171 H UNK 0 6.818 -2.856 -2.264 0.00 0.00 H+0 HETATM 172 H UNK 0 8.525 -2.789 -1.722 0.00 0.00 H+0 HETATM 173 H UNK 0 8.079 -3.366 -3.423 0.00 0.00 H+0 HETATM 174 H UNK 0 7.563 -0.184 -4.972 0.00 0.00 H+0 HETATM 175 H UNK 0 6.417 -1.526 -4.692 0.00 0.00 H+0 HETATM 176 H UNK 0 8.589 -1.575 -6.442 0.00 0.00 H+0 HETATM 177 H UNK 0 9.364 -2.235 -4.988 0.00 0.00 H+0 HETATM 178 H UNK 0 7.931 -3.094 -5.671 0.00 0.00 H+0 HETATM 179 H UNK 0 3.356 -1.799 -3.183 0.00 0.00 H+0 HETATM 180 H UNK 0 1.293 -2.785 -2.626 0.00 0.00 H+0 HETATM 181 H UNK 0 0.868 -1.546 -1.441 0.00 0.00 H+0 HETATM 182 H UNK 0 1.002 -1.099 -3.225 0.00 0.00 H+0 HETATM 183 H UNK 0 4.143 -3.048 -1.403 0.00 0.00 H+0 HETATM 184 H UNK 0 2.524 -2.932 -0.701 0.00 0.00 H+0 HETATM 185 H UNK 0 3.807 -1.646 -0.306 0.00 0.00 H+0 HETATM 186 H UNK 0 2.073 3.647 0.807 0.00 0.00 H+0 HETATM 187 H UNK 0 3.105 1.030 2.139 0.00 0.00 H+0 HETATM 188 H UNK 0 3.948 2.100 0.946 0.00 0.00 H+0 HETATM 189 H UNK 0 3.599 2.666 2.618 0.00 0.00 H+0 HETATM 190 H UNK 0 0.417 3.784 2.561 0.00 0.00 H+0 HETATM 191 H UNK 0 0.715 2.091 3.103 0.00 0.00 H+0 HETATM 192 H UNK 0 1.944 3.390 3.422 0.00 0.00 H+0 CONECT 1 2 83 84 85 CONECT 2 1 3 86 87 CONECT 3 2 4 88 89 CONECT 4 3 5 90 91 CONECT 5 4 6 92 93 CONECT 6 5 7 94 95 CONECT 7 6 8 96 97 CONECT 8 7 9 98 99 CONECT 9 8 10 11 100 CONECT 10 9 101 102 103 CONECT 11 9 12 13 CONECT 12 11 CONECT 13 11 14 17 CONECT 14 13 15 104 105 CONECT 15 14 16 106 107 CONECT 16 15 17 108 109 CONECT 17 16 18 13 110 CONECT 18 17 19 20 CONECT 19 18 CONECT 20 18 21 111 CONECT 21 20 22 33 112 CONECT 22 21 23 113 114 CONECT 23 22 24 25 115 CONECT 24 23 116 117 118 CONECT 25 23 26 119 120 CONECT 26 25 27 28 121 CONECT 27 26 122 CONECT 28 26 29 123 124 CONECT 29 28 30 31 CONECT 30 29 CONECT 31 29 32 125 126 CONECT 32 31 127 128 129 CONECT 33 21 34 35 CONECT 34 33 CONECT 35 33 36 130 CONECT 36 35 37 38 131 CONECT 37 36 132 133 134 CONECT 38 36 39 40 CONECT 39 38 CONECT 40 38 41 135 CONECT 41 40 42 80 136 CONECT 42 41 43 44 CONECT 43 42 CONECT 44 42 45 137 CONECT 45 44 46 77 138 CONECT 46 45 47 48 CONECT 47 46 CONECT 48 46 49 139 CONECT 49 48 50 73 140 CONECT 50 49 51 52 CONECT 51 50 CONECT 52 50 53 141 CONECT 53 52 54 55 56 CONECT 54 53 142 143 144 CONECT 55 53 145 146 147 CONECT 56 53 57 58 CONECT 57 56 CONECT 58 56 59 148 CONECT 59 58 60 61 62 CONECT 60 59 149 150 151 CONECT 61 59 152 153 154 CONECT 62 59 63 64 CONECT 63 62 CONECT 64 62 65 155 CONECT 65 64 66 67 156 CONECT 66 65 157 158 159 CONECT 67 65 68 160 161 CONECT 68 67 69 70 CONECT 69 68 162 163 164 CONECT 70 68 71 165 166 CONECT 71 70 72 167 168 CONECT 72 71 169 CONECT 73 49 74 75 170 CONECT 74 73 171 172 173 CONECT 75 73 76 174 175 CONECT 76 75 176 177 178 CONECT 77 45 78 79 179 CONECT 78 77 180 181 182 CONECT 79 77 183 184 185 CONECT 80 41 81 82 186 CONECT 81 80 187 188 189 CONECT 82 80 190 191 192 CONECT 83 1 CONECT 84 1 CONECT 85 1 CONECT 86 2 CONECT 87 2 CONECT 88 3 CONECT 89 3 CONECT 90 4 CONECT 91 4 CONECT 92 5 CONECT 93 5 CONECT 94 6 CONECT 95 6 CONECT 96 7 CONECT 97 7 CONECT 98 8 CONECT 99 8 CONECT 100 9 CONECT 101 10 CONECT 102 10 CONECT 103 10 CONECT 104 14 CONECT 105 14 CONECT 106 15 CONECT 107 15 CONECT 108 16 CONECT 109 16 CONECT 110 17 CONECT 111 20 CONECT 112 21 CONECT 113 22 CONECT 114 22 CONECT 115 23 CONECT 116 24 CONECT 117 24 CONECT 118 24 CONECT 119 25 CONECT 120 25 CONECT 121 26 CONECT 122 27 CONECT 123 28 CONECT 124 28 CONECT 125 31 CONECT 126 31 CONECT 127 32 CONECT 128 32 CONECT 129 32 CONECT 130 35 CONECT 131 36 CONECT 132 37 CONECT 133 37 CONECT 134 37 CONECT 135 40 CONECT 136 41 CONECT 137 44 CONECT 138 45 CONECT 139 48 CONECT 140 49 CONECT 141 52 CONECT 142 54 CONECT 143 54 CONECT 144 54 CONECT 145 55 CONECT 146 55 CONECT 147 55 CONECT 148 58 CONECT 149 60 CONECT 150 60 CONECT 151 60 CONECT 152 61 CONECT 153 61 CONECT 154 61 CONECT 155 64 CONECT 156 65 CONECT 157 66 CONECT 158 66 CONECT 159 66 CONECT 160 67 CONECT 161 67 CONECT 162 69 CONECT 163 69 CONECT 164 69 CONECT 165 70 CONECT 166 70 CONECT 167 71 CONECT 168 71 CONECT 169 72 CONECT 170 73 CONECT 171 74 CONECT 172 74 CONECT 173 74 CONECT 174 75 CONECT 175 75 CONECT 176 76 CONECT 177 76 CONECT 178 76 CONECT 179 77 CONECT 180 78 CONECT 181 78 CONECT 182 78 CONECT 183 79 CONECT 184 79 CONECT 185 79 CONECT 186 80 CONECT 187 81 CONECT 188 81 CONECT 189 81 CONECT 190 82 CONECT 191 82 CONECT 192 82 MASTER 0 0 0 0 0 0 0 0 192 0 384 0 END SMILES for NP0003268 (Roseoferin C2)[H]OC([H])([H])C([H])([H])N(C([H])([H])[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@]([H])(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])(C([H])([H])[H])C([H])([H])[H])C([H])(C([H])([H])[H])C([H])([H])[H])[C@@]([H])(C([H])([H])[H])C([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 NP0003268 (Roseoferin C2)InChI=1S/C60H110N10O12/c1-18-21-22-23-24-25-27-40(10)56(80)70-29-26-28-46(70)52(76)63-45(33-38(8)32-44(73)34-43(72)20-3)51(75)62-42(12)50(74)64-47(36(4)5)53(77)65-48(37(6)7)54(78)66-49(39(9)19-2)55(79)67-60(15,16)58(82)68-59(13,14)57(81)61-41(11)35-69(17)30-31-71/h36-42,44-49,71,73H,18-35H2,1-17H3,(H,61,81)(H,62,75)(H,63,76)(H,64,74)(H,65,77)(H,66,78)(H,67,79)(H,68,82)/t38-,39+,40-,41-,42+,44-,45-,46+,47-,48-,49-/m1/s1 3D Structure for NP0003268 (Roseoferin C2) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms |
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| Chemical Formula | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Average Mass | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Monoisotopic Mass | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| IUPAC Name | (2R,4S)-6-hydroxy-N-[(1S)-1-{[(1R)-1-{[(1R)-1-{[(1R,2S)-1-({1-[(1-{[(2R)-1-[(2-hydroxyethyl)(methyl)amino]propan-2-yl]carbamoyl}-1-methylethyl)carbamoyl]-1-methylethyl}carbamoyl)-2-methylbutyl]carbamoyl}-2-methylpropyl]carbamoyl}-2-methylpropyl]carbamoyl}ethyl]-4-methyl-2-{[(2S)-1-[(2R)-2-methyldecanoyl]pyrrolidin-2-yl]formamido}-8-oxodecanamide | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Traditional Name | (2R,4S)-6-hydroxy-N-[(1S)-1-{[(1R)-1-{[(1R)-1-{[(1R,2S)-1-({1-[(1-{[(2R)-1-[(2-hydroxyethyl)(methyl)amino]propan-2-yl]carbamoyl}-1-methylethyl)carbamoyl]-1-methylethyl}carbamoyl)-2-methylbutyl]carbamoyl}-2-methylpropyl]carbamoyl}-2-methylpropyl]carbamoyl}ethyl]-4-methyl-2-{[(2S)-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)C(=O)NC(C(C)C)C(=O)NC(C(C)CC)C(=O)NC(C)(C)C(=O)NC(C)(C)C(=O)NC(C)CN(C)CCO | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Identifier | InChI=1S/C60H110N10O12/c1-18-21-22-23-24-25-27-40(10)56(80)70-29-26-28-46(70)52(76)63-45(33-38(8)32-44(73)34-43(72)20-3)51(75)62-42(12)50(74)64-47(36(4)5)53(77)65-48(37(6)7)54(78)66-49(39(9)19-2)55(79)67-60(15,16)58(82)68-59(13,14)57(81)61-41(11)35-69(17)30-31-71/h36-42,44-49,71,73H,18-35H2,1-17H3,(H,61,81)(H,62,75)(H,63,76)(H,64,74)(H,65,77)(H,66,78)(H,67,79)(H,68,82) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Key | DEGMKTXWWRMWKD-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 | NPA010563 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HMDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DrugBank ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Phenol Explorer Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| FoodDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| KNApSAcK ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemspider ID | 78444819 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| KEGG Compound ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BioCyc ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BiGG ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Wikipedia Link | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| METLIN ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| PubChem Compound | 85203673 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| PDB ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| ChEBI ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Good Scents ID | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| General References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
