Showing NP-Card for carteraol E (NP0038124)
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| Version | 2.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Created at | 2021-06-20 20:53:53 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Updated at | 2021-06-30 00:10:44 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| NP-MRD ID | NP0038124 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Common Name | carteraol E | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Provided By | JEOL Database | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | carteraol E is found in Amphidinium carterae. carteraol E was first documented in 2009 (Huang, S.-J., et al.). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structure |  MOL for NP0038124 (carteraol E)
Mrv1652306202122533D
224226 0 0 0 0 999 V2000
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31135 1 0 0 0 0
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37142 1 0 0 0 0
M END
3D MOL for NP0038124 (carteraol E)
RDKit 3D
224226 0 0 0 0 0 0 0 0999 V2000
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35140 1 0
37142 1 0
M END
3D SDF for NP0038124 (carteraol E)
Mrv1652306202122533D
224226 0 0 0 0 999 V2000
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50158 1 0 0 0 0
50159 1 0 0 0 0
49156 1 0 0 0 0
49157 1 0 0 0 0
47154 1 6 0 0 0
87212 1 0 0 0 0
92216 1 0 0 0 0
92217 1 0 0 0 0
92218 1 0 0 0 0
67181 1 0 0 0 0
67182 1 0 0 0 0
67183 1 0 0 0 0
64177 1 0 0 0 0
62175 1 0 0 0 0
59169 1 0 0 0 0
59170 1 0 0 0 0
59171 1 0 0 0 0
57167 1 0 0 0 0
55165 1 0 0 0 0
52161 1 0 0 0 0
48155 1 0 0 0 0
46152 1 0 0 0 0
46153 1 0 0 0 0
43148 1 0 0 0 0
45149 1 0 0 0 0
45150 1 0 0 0 0
45151 1 0 0 0 0
41146 1 6 0 0 0
39144 1 6 0 0 0
40145 1 0 0 0 0
42147 1 0 0 0 0
30134 1 1 0 0 0
29132 1 0 0 0 0
29133 1 0 0 0 0
28130 1 0 0 0 0
28131 1 0 0 0 0
24126 1 6 0 0 0
22124 1 6 0 0 0
27128 1 0 0 0 0
27129 1 0 0 0 0
25127 1 0 0 0 0
23125 1 0 0 0 0
17120 1 6 0 0 0
15118 1 1 0 0 0
14117 1 0 0 0 0
13116 1 0 0 0 0
12114 1 0 0 0 0
12115 1 0 0 0 0
11112 1 0 0 0 0
11113 1 0 0 0 0
10111 1 0 0 0 0
9110 1 0 0 0 0
8109 1 0 0 0 0
7108 1 0 0 0 0
6107 1 0 0 0 0
5106 1 0 0 0 0
4104 1 0 0 0 0
4105 1 0 0 0 0
3102 1 0 0 0 0
3103 1 0 0 0 0
2101 1 0 0 0 0
1 99 1 0 0 0 0
1100 1 0 0 0 0
16119 1 0 0 0 0
18121 1 0 0 0 0
98224 1 0 0 0 0
96222 1 0 0 0 0
31135 1 0 0 0 0
35140 1 0 0 0 0
37142 1 0 0 0 0
M END
> <DATABASE_ID>
NP0038124
> <DATABASE_NAME>
NP-MRD
> <SMILES>
[H]OC([H])([H])[C@]([H])(O[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])O[C@@]([H])(C([H])([H])C(=O)C([H])([H])[C@]([H])(OC([H])([H])[H])C([H])([H])C([H])([H])C(\[H])=C(/[H])[C@]([H])(C([H])([H])[H])C([H])([H])[C@]([H])(O[H])[C@]([H])(O[H])C([H])([H])[C@@]([H])(C([H])([H])[H])[C@@]([H])(O[H])[C@]([H])(O[H])C([H])([H])[C@]([H])(O[H])C([H])([H])C([H])([H])[C@@]([H])(O[H])C([H])([H])C(=C(/[H])[C@@]([H])(O[H])[C@@]([H])(O[H])[C@@]2([H])O[C@]([H])(C([H])([H])[C@@]([H])(O[H])[C@@]2([H])O[H])[C@@]([H])(O[H])C([H])([H])C([H])([H])C(=C([H])[H])[C@@]([H])(O[H])[C@]([H])(O[H])[C@]2([H])O[C@@]([H])([C@]([H])(O[H])[C@@]([H])(O[H])C(\[H])=C(/[H])C([H])([H])C([H])([H])C(\[H])=C(/[H])\C(\[H])=C(/[H])\C(\[H])=C(/[H])C([H])([H])C([H])([H])C([H])=C([H])[H])[C@]([H])(O[H])[C@]([H])(O[H])C2([H])[H])\C([H])([H])[H])C([H])([H])C([H])([H])C1([H])[H]
> <INCHI_IDENTIFIER>
InChI=1S/C74H126O24/c1-7-8-9-10-11-12-13-14-15-16-17-18-30-57(81)68(90)73-71(93)63(87)43-65(98-73)72(94)67(89)47(4)31-34-56(80)64-42-62(86)70(92)74(97-64)69(91)60(84)37-46(3)35-49(76)32-33-50(77)41-61(85)66(88)48(5)38-59(83)58(82)36-45(2)24-19-21-27-54(95-6)39-52(79)40-55-29-23-28-53(96-55)26-22-20-25-51(78)44-75/h7,10-15,18-19,24,30,37,45,48-51,53-78,80-94H,1,4,8-9,16-17,20-23,25-29,31-36,38-44H2,2-3,5-6H3/b11-10+,13-12+,15-14+,24-19+,30-18+,46-37+/t45-,48+,49+,50+,51+,53+,54+,55+,56-,57-,58-,59+,60+,61+,62+,63+,64+,65+,66+,67+,68+,69+,70+,71+,72+,73-,74+/m0/s1
> <INCHI_KEY>
FMPBABOEFWIINO-DMQQLDSRSA-N
> <FORMULA>
C74H126O24
> <MOLECULAR_WEIGHT>
1399.798
> <EXACT_MASS>
1398.863904937
> <JCHEM_ACCEPTOR_COUNT>
24
> <JCHEM_ATOM_COUNT>
224
> <JCHEM_AVERAGE_POLARIZABILITY>
151.93605124732287
> <JCHEM_BIOAVAILABILITY>
0
> <JCHEM_DONOR_COUNT>
19
> <JCHEM_FORMAL_CHARGE>
0
> <JCHEM_GHOSE_FILTER>
0
> <JCHEM_IUPAC>
(4R,7E,9R,11S,12R,14R,15R,16R,18R,21R,23E,25R,26R)-26-[(2S,3R,4R,6R)-6-[(1S,5R,6S)-6-[(2R,4R,5R,6R)-6-[(1R,2S,3E,7E,9E,11E)-1,2-dihydroxyhexadeca-3,7,9,11,15-pentaen-1-yl]-4,5-dihydroxyoxan-2-yl]-1,5,6-trihydroxy-4-methylidenehexyl]-3,4-dihydroxyoxan-2-yl]-1-[(2R,6R)-6-[(5R)-5,6-dihydroxyhexyl]oxan-2-yl]-11,12,15,16,18,21,25,26-octahydroxy-4-methoxy-9,14,23-trimethylhexacosa-7,23-dien-2-one
> <ALOGPS_LOGP>
1.89
> <JCHEM_LOGP>
1.2691142066666665
> <ALOGPS_LOGS>
-4.47
> <JCHEM_MDDR_LIKE_RULE>
1
> <JCHEM_NUMBER_OF_RINGS>
3
> <JCHEM_PHYSIOLOGICAL_CHARGE>
0
> <JCHEM_PKA>
12.760619180778448
> <JCHEM_PKA_STRONGEST_ACIDIC>
12.350191706789317
> <JCHEM_PKA_STRONGEST_BASIC>
-3.34306721297974
> <JCHEM_POLAR_SURFACE_AREA>
438.3600000000001
> <JCHEM_REFRACTIVITY>
376.9588999999999
> <JCHEM_ROTATABLE_BOND_COUNT>
50
> <JCHEM_RULE_OF_FIVE>
0
> <ALOGPS_SOLUBILITY>
4.70e-02 g/l
> <JCHEM_TRADITIONAL_IUPAC>
(4R,7E,9R,11S,12R,14R,15R,16R,18R,21R,23E,25R,26R)-26-[(2S,3R,4R,6R)-6-[(1S,5R,6S)-6-[(2R,4R,5R,6R)-6-[(1R,2S,3E,7E,9E,11E)-1,2-dihydroxyhexadeca-3,7,9,11,15-pentaen-1-yl]-4,5-dihydroxyoxan-2-yl]-1,5,6-trihydroxy-4-methylidenehexyl]-3,4-dihydroxyoxan-2-yl]-1-[(2R,6R)-6-[(5R)-5,6-dihydroxyhexyl]oxan-2-yl]-11,12,15,16,18,21,25,26-octahydroxy-4-methoxy-9,14,23-trimethylhexacosa-7,23-dien-2-one
> <JCHEM_VEBER_RULE>
0
$$$$
3D-SDF for NP0038124 (carteraol E)
RDKit 3D
224226 0 0 0 0 0 0 0 0999 V2000
-3.7412 1.0088 -6.7605 C 0 0 0 0 0 0 0 0 0 0 0 0
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0.5518 0.4533 -5.4570 C 0 0 0 0 0 0 0 0 0 0 0 0
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2.5586 -0.4648 -4.3516 C 0 0 0 0 0 0 0 0 0 0 0 0
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5.3719 -2.6666 -1.4255 C 0 0 0 0 0 0 0 0 0 0 0 0
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2.8432 -5.1509 1.7370 C 0 0 2 0 0 0 0 0 0 0 0 0
3.0558 -5.3231 3.1464 O 0 0 0 0 0 0 0 0 0 0 0 0
2.7748 -6.5619 1.1048 C 0 0 1 0 0 0 0 0 0 0 0 0
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1.1100 3.0673 2.1548 C 0 0 1 0 0 0 0 0 0 0 0 0
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2.0688 3.4756 1.0227 C 0 0 1 0 0 0 0 0 0 0 0 0
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4.6008 2.9418 -1.0613 C 0 0 2 0 0 0 0 0 0 0 0 0
5.2151 3.6868 0.0033 O 0 0 0 0 0 0 0 0 0 0 0 0
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3.9077 3.9587 -3.3164 C 0 0 0 0 0 0 0 0 0 0 0 0
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1.3572 -1.1275 4.9398 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8180 -1.5114 4.6666 C 0 0 1 0 0 0 0 0 0 0 0 0
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3.5868 -0.3797 3.9677 C 0 0 0 0 0 0 0 0 0 0 0 0
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1.4604 1.1894 0.2912 O 0 0 0 0 0 0 0 0 0 0 0 0
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1.8350 -7.8469 -2.4608 C 0 0 1 0 0 0 0 0 0 0 0 0
3.0445 -7.7599 -3.2223 O 0 0 0 0 0 0 0 0 0 0 0 0
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2.3403 0.0009 -6.4545 H 0 0 0 0 0 0 0 0 0 0 0 0
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4.3391 -0.7757 -5.4323 H 0 0 0 0 0 0 0 0 0 0 0 0
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3.3598 -2.5395 -2.3639 H 0 0 0 0 0 0 0 0 0 0 0 0
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2.8676 -2.7692 0.3239 H 0 0 0 0 0 0 0 0 0 0 0 0
4.9811 -4.7149 1.4250 H 0 0 0 0 0 0 0 0 0 0 0 0
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3.0566 -4.4140 3.5280 H 0 0 0 0 0 0 0 0 0 0 0 0
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5.2802 3.2829 -4.8143 H 0 0 0 0 0 0 0 0 0 0 0 0
3.2022 6.0009 -3.3950 H 0 0 0 0 0 0 0 0 0 0 0 0
3.8762 5.4276 -4.8830 H 0 0 0 0 0 0 0 0 0 0 0 0
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1.8763 6.2761 -5.8798 H 0 0 0 0 0 0 0 0 0 0 0 0
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M END
PDB for NP0038124 (carteraol E)HEADER PROTEIN 20-JUN-21 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 20-JUN-21 0 HETATM 1 C UNK 0 -3.741 1.009 -6.761 0.00 0.00 C+0 HETATM 2 C UNK 0 -2.615 0.510 -6.236 0.00 0.00 C+0 HETATM 3 C UNK 0 -1.408 0.129 -7.047 0.00 0.00 C+0 HETATM 4 C UNK 0 -0.167 0.956 -6.684 0.00 0.00 C+0 HETATM 5 C UNK 0 0.552 0.453 -5.457 0.00 0.00 C+0 HETATM 6 C UNK 0 1.816 0.008 -5.500 0.00 0.00 C+0 HETATM 7 C UNK 0 2.559 -0.465 -4.352 0.00 0.00 C+0 HETATM 8 C UNK 0 3.842 -0.841 -4.465 0.00 0.00 C+0 HETATM 9 C UNK 0 4.706 -1.285 -3.398 0.00 0.00 C+0 HETATM 10 C UNK 0 4.372 -2.144 -2.424 0.00 0.00 C+0 HETATM 11 C UNK 0 5.372 -2.667 -1.426 0.00 0.00 C+0 HETATM 12 C UNK 0 5.019 -2.373 0.036 0.00 0.00 C+0 HETATM 13 C UNK 0 3.853 -3.182 0.531 0.00 0.00 C+0 HETATM 14 C UNK 0 3.984 -4.331 1.213 0.00 0.00 C+0 HETATM 15 C UNK 0 2.843 -5.151 1.737 0.00 0.00 C+0 HETATM 16 O UNK 0 3.056 -5.323 3.146 0.00 0.00 O+0 HETATM 17 C UNK 0 2.775 -6.562 1.105 0.00 0.00 C+0 HETATM 18 O UNK 0 1.858 -7.369 1.872 0.00 0.00 O+0 HETATM 19 C UNK 0 2.348 -6.546 -0.379 0.00 0.00 C+0 HETATM 20 O UNK 0 1.151 -5.747 -0.518 0.00 0.00 O+0 HETATM 21 C UNK 0 0.223 -6.171 -1.541 0.00 0.00 C+0 HETATM 22 C UNK 0 -0.781 -5.019 -1.794 0.00 0.00 C+0 HETATM 23 O UNK 0 -1.549 -4.891 -0.582 0.00 0.00 O+0 HETATM 24 C UNK 0 -0.113 -3.653 -2.137 0.00 0.00 C+0 HETATM 25 O UNK 0 0.780 -3.241 -1.100 0.00 0.00 O+0 HETATM 26 C UNK 0 -1.120 -2.535 -2.357 0.00 0.00 C+0 HETATM 27 C UNK 0 -1.658 -2.314 -3.570 0.00 0.00 C+0 HETATM 28 C UNK 0 -1.522 -1.680 -1.168 0.00 0.00 C+0 HETATM 29 C UNK 0 -0.596 -0.469 -0.989 0.00 0.00 C+0 HETATM 30 C UNK 0 -0.825 0.266 0.344 0.00 0.00 C+0 HETATM 31 O UNK 0 -2.205 0.650 0.444 0.00 0.00 O+0 HETATM 32 C UNK 0 0.074 1.522 0.434 0.00 0.00 C+0 HETATM 33 C UNK 0 -0.131 2.297 1.732 0.00 0.00 C+0 HETATM 34 C UNK 0 1.110 3.067 2.155 0.00 0.00 C+0 HETATM 35 O UNK 0 1.851 2.263 3.102 0.00 0.00 O+0 HETATM 36 C UNK 0 2.069 3.476 1.023 0.00 0.00 C+0 HETATM 37 O UNK 0 3.270 3.880 1.696 0.00 0.00 O+0 HETATM 38 C UNK 0 2.236 2.367 -0.054 0.00 0.00 C+0 HETATM 39 C UNK 0 3.654 1.884 -0.436 0.00 0.00 C+0 HETATM 40 O UNK 0 4.335 1.317 0.702 0.00 0.00 O+0 HETATM 41 C UNK 0 4.601 2.942 -1.061 0.00 0.00 C+0 HETATM 42 O UNK 0 5.215 3.687 0.003 0.00 0.00 O+0 HETATM 43 C UNK 0 3.970 3.957 -1.969 0.00 0.00 C+0 HETATM 44 C UNK 0 3.908 3.959 -3.316 0.00 0.00 C+0 HETATM 45 C UNK 0 4.468 2.881 -4.200 0.00 0.00 C+0 HETATM 46 C UNK 0 3.240 5.115 -4.044 0.00 0.00 C+0 HETATM 47 C UNK 0 1.816 4.828 -4.566 0.00 0.00 C+0 HETATM 48 O UNK 0 1.288 6.019 -5.150 0.00 0.00 O+0 HETATM 49 C UNK 0 0.882 4.362 -3.444 0.00 0.00 C+0 HETATM 50 C UNK 0 -0.585 4.217 -3.864 0.00 0.00 C+0 HETATM 51 C UNK 0 -1.364 3.429 -2.806 0.00 0.00 C+0 HETATM 52 O UNK 0 -1.314 4.138 -1.564 0.00 0.00 O+0 HETATM 53 C UNK 0 -2.818 3.164 -3.217 0.00 0.00 C+0 HETATM 54 C UNK 0 -3.469 2.124 -2.286 0.00 0.00 C+0 HETATM 55 O UNK 0 -3.480 2.656 -0.955 0.00 0.00 O+0 HETATM 56 C UNK 0 -4.873 1.678 -2.768 0.00 0.00 C+0 HETATM 57 O UNK 0 -5.608 2.789 -3.273 0.00 0.00 O+0 HETATM 58 C UNK 0 -5.657 0.823 -1.736 0.00 0.00 C+0 HETATM 59 C UNK 0 -6.721 -0.023 -2.460 0.00 0.00 C+0 HETATM 60 C UNK 0 -6.272 1.549 -0.506 0.00 0.00 C+0 HETATM 61 C UNK 0 -7.016 2.872 -0.747 0.00 0.00 C+0 HETATM 62 O UNK 0 -7.890 2.710 -1.879 0.00 0.00 O+0 HETATM 63 C UNK 0 -7.899 3.338 0.431 0.00 0.00 C+0 HETATM 64 O UNK 0 -8.964 2.375 0.579 0.00 0.00 O+0 HETATM 65 C UNK 0 -7.197 3.510 1.778 0.00 0.00 C+0 HETATM 66 C UNK 0 -6.042 4.529 1.813 0.00 0.00 C+0 HETATM 67 C UNK 0 -6.455 5.912 1.309 0.00 0.00 C+0 HETATM 68 C UNK 0 -5.558 4.647 3.241 0.00 0.00 C+0 HETATM 69 C UNK 0 -4.314 4.349 3.649 0.00 0.00 C+0 HETATM 70 C UNK 0 -3.884 4.408 5.091 0.00 0.00 C+0 HETATM 71 C UNK 0 -3.552 3.008 5.622 0.00 0.00 C+0 HETATM 72 C UNK 0 -2.126 2.569 5.237 0.00 0.00 C+0 HETATM 73 C UNK 0 -1.972 1.049 5.291 0.00 0.00 C+0 HETATM 74 C UNK 0 -2.860 0.363 4.270 0.00 0.00 C+0 HETATM 75 O UNK 0 -2.849 0.701 3.083 0.00 0.00 O+0 HETATM 76 C UNK 0 -3.772 -0.737 4.777 0.00 0.00 C+0 HETATM 77 C UNK 0 -3.420 -2.114 4.228 0.00 0.00 C+0 HETATM 78 C UNK 0 -3.877 -2.316 2.783 0.00 0.00 C+0 HETATM 79 C UNK 0 -3.521 -3.725 2.329 0.00 0.00 C+0 HETATM 80 C UNK 0 -2.042 -3.993 2.570 0.00 0.00 C+0 HETATM 81 C UNK 0 -1.623 -3.663 4.008 0.00 0.00 C+0 HETATM 82 C UNK 0 -0.100 -3.819 4.126 0.00 0.00 C+0 HETATM 83 C UNK 0 0.490 -3.533 5.511 0.00 0.00 C+0 HETATM 84 C UNK 0 0.621 -2.061 5.913 0.00 0.00 C+0 HETATM 85 C UNK 0 1.357 -1.127 4.940 0.00 0.00 C+0 HETATM 86 C UNK 0 2.818 -1.511 4.667 0.00 0.00 C+0 HETATM 87 O UNK 0 2.858 -2.650 3.797 0.00 0.00 O+0 HETATM 88 C UNK 0 3.587 -0.380 3.968 0.00 0.00 C+0 HETATM 89 O UNK 0 3.003 -0.130 2.684 0.00 0.00 O+0 HETATM 90 O UNK 0 -2.008 -2.325 4.344 0.00 0.00 O+0 HETATM 91 O UNK 0 -1.258 3.172 6.213 0.00 0.00 O+0 HETATM 92 C UNK 0 0.076 3.350 5.759 0.00 0.00 C+0 HETATM 93 O UNK 0 1.460 1.189 0.291 0.00 0.00 O+0 HETATM 94 C UNK 0 0.972 -6.624 -2.787 0.00 0.00 C+0 HETATM 95 C UNK 0 1.835 -7.847 -2.461 0.00 0.00 C+0 HETATM 96 O UNK 0 3.045 -7.760 -3.222 0.00 0.00 O+0 HETATM 97 C UNK 0 2.167 -7.960 -0.959 0.00 0.00 C+0 HETATM 98 O UNK 0 3.335 -8.774 -0.812 0.00 0.00 O+0 HETATM 99 H UNK 0 -3.854 1.172 -7.828 0.00 0.00 H+0 HETATM 100 H UNK 0 -4.582 1.279 -6.128 0.00 0.00 H+0 HETATM 101 H UNK 0 -2.553 0.371 -5.161 0.00 0.00 H+0 HETATM 102 H UNK 0 -1.621 0.278 -8.113 0.00 0.00 H+0 HETATM 103 H UNK 0 -1.210 -0.942 -6.915 0.00 0.00 H+0 HETATM 104 H UNK 0 -0.436 2.008 -6.534 0.00 0.00 H+0 HETATM 105 H UNK 0 0.515 0.935 -7.544 0.00 0.00 H+0 HETATM 106 H UNK 0 0.009 0.477 -4.515 0.00 0.00 H+0 HETATM 107 H UNK 0 2.340 0.001 -6.455 0.00 0.00 H+0 HETATM 108 H UNK 0 2.052 -0.497 -3.389 0.00 0.00 H+0 HETATM 109 H UNK 0 4.339 -0.776 -5.432 0.00 0.00 H+0 HETATM 110 H UNK 0 5.735 -0.935 -3.473 0.00 0.00 H+0 HETATM 111 H UNK 0 3.360 -2.539 -2.364 0.00 0.00 H+0 HETATM 112 H UNK 0 5.475 -3.749 -1.575 0.00 0.00 H+0 HETATM 113 H UNK 0 6.361 -2.235 -1.628 0.00 0.00 H+0 HETATM 114 H UNK 0 5.899 -2.585 0.656 0.00 0.00 H+0 HETATM 115 H UNK 0 4.799 -1.309 0.173 0.00 0.00 H+0 HETATM 116 H UNK 0 2.868 -2.769 0.324 0.00 0.00 H+0 HETATM 117 H UNK 0 4.981 -4.715 1.425 0.00 0.00 H+0 HETATM 118 H UNK 0 1.881 -4.637 1.634 0.00 0.00 H+0 HETATM 119 H UNK 0 3.057 -4.414 3.528 0.00 0.00 H+0 HETATM 120 H UNK 0 3.751 -7.053 1.206 0.00 0.00 H+0 HETATM 121 H UNK 0 2.008 -7.081 2.799 0.00 0.00 H+0 HETATM 122 H UNK 0 3.137 -6.031 -0.943 0.00 0.00 H+0 HETATM 123 H UNK 0 -0.347 -7.012 -1.123 0.00 0.00 H+0 HETATM 124 H UNK 0 -1.481 -5.308 -2.586 0.00 0.00 H+0 HETATM 125 H UNK 0 -0.916 -4.545 0.076 0.00 0.00 H+0 HETATM 126 H UNK 0 0.493 -3.769 -3.043 0.00 0.00 H+0 HETATM 127 H UNK 0 1.256 -4.045 -0.813 0.00 0.00 H+0 HETATM 128 H UNK 0 -2.392 -1.531 -3.724 0.00 0.00 H+0 HETATM 129 H UNK 0 -1.385 -2.911 -4.436 0.00 0.00 H+0 HETATM 130 H UNK 0 -2.555 -1.330 -1.298 0.00 0.00 H+0 HETATM 131 H UNK 0 -1.532 -2.287 -0.257 0.00 0.00 H+0 HETATM 132 H UNK 0 0.454 -0.773 -1.053 0.00 0.00 H+0 HETATM 133 H UNK 0 -0.770 0.220 -1.823 0.00 0.00 H+0 HETATM 134 H UNK 0 -0.593 -0.426 1.164 0.00 0.00 H+0 HETATM 135 H UNK 0 -2.418 0.654 1.409 0.00 0.00 H+0 HETATM 136 H UNK 0 -0.216 2.176 -0.395 0.00 0.00 H+0 HETATM 137 H UNK 0 -0.976 2.984 1.598 0.00 0.00 H+0 HETATM 138 H UNK 0 -0.408 1.608 2.538 0.00 0.00 H+0 HETATM 139 H UNK 0 0.814 3.961 2.714 0.00 0.00 H+0 HETATM 140 H UNK 0 2.728 2.715 3.122 0.00 0.00 H+0 HETATM 141 H UNK 0 1.668 4.368 0.526 0.00 0.00 H+0 HETATM 142 H UNK 0 3.915 4.182 1.020 0.00 0.00 H+0 HETATM 143 H UNK 0 1.782 2.746 -0.976 0.00 0.00 H+0 HETATM 144 H UNK 0 3.538 1.067 -1.160 0.00 0.00 H+0 HETATM 145 H UNK 0 3.696 0.708 1.139 0.00 0.00 H+0 HETATM 146 H UNK 0 5.430 2.426 -1.558 0.00 0.00 H+0 HETATM 147 H UNK 0 5.516 2.982 0.622 0.00 0.00 H+0 HETATM 148 H UNK 0 3.528 4.806 -1.445 0.00 0.00 H+0 HETATM 149 H UNK 0 3.692 2.496 -4.868 0.00 0.00 H+0 HETATM 150 H UNK 0 4.864 2.032 -3.639 0.00 0.00 H+0 HETATM 151 H UNK 0 5.280 3.283 -4.814 0.00 0.00 H+0 HETATM 152 H UNK 0 3.202 6.001 -3.395 0.00 0.00 H+0 HETATM 153 H UNK 0 3.876 5.428 -4.883 0.00 0.00 H+0 HETATM 154 H UNK 0 1.847 4.064 -5.352 0.00 0.00 H+0 HETATM 155 H UNK 0 1.876 6.276 -5.880 0.00 0.00 H+0 HETATM 156 H UNK 0 0.933 5.071 -2.608 0.00 0.00 H+0 HETATM 157 H UNK 0 1.237 3.392 -3.078 0.00 0.00 H+0 HETATM 158 H UNK 0 -0.646 3.699 -4.827 0.00 0.00 H+0 HETATM 159 H UNK 0 -1.025 5.213 -3.990 0.00 0.00 H+0 HETATM 160 H UNK 0 -0.861 2.468 -2.653 0.00 0.00 H+0 HETATM 161 H UNK 0 -2.137 3.899 -1.082 0.00 0.00 H+0 HETATM 162 H UNK 0 -2.853 2.803 -4.250 0.00 0.00 H+0 HETATM 163 H UNK 0 -3.375 4.107 -3.160 0.00 0.00 H+0 HETATM 164 H UNK 0 -2.836 1.229 -2.265 0.00 0.00 H+0 HETATM 165 H UNK 0 -3.216 1.907 -0.371 0.00 0.00 H+0 HETATM 166 H UNK 0 -4.693 1.047 -3.647 0.00 0.00 H+0 HETATM 167 H UNK 0 -6.559 2.667 -3.067 0.00 0.00 H+0 HETATM 168 H UNK 0 -4.948 0.089 -1.326 0.00 0.00 H+0 HETATM 169 H UNK 0 -6.243 -0.698 -3.179 0.00 0.00 H+0 HETATM 170 H UNK 0 -7.276 -0.648 -1.752 0.00 0.00 H+0 HETATM 171 H UNK 0 -7.440 0.584 -3.015 0.00 0.00 H+0 HETATM 172 H UNK 0 -6.951 0.841 -0.014 0.00 0.00 H+0 HETATM 173 H UNK 0 -5.479 1.730 0.229 0.00 0.00 H+0 HETATM 174 H UNK 0 -6.298 3.661 -0.992 0.00 0.00 H+0 HETATM 175 H UNK 0 -8.684 2.267 -1.508 0.00 0.00 H+0 HETATM 176 H UNK 0 -8.398 4.271 0.143 0.00 0.00 H+0 HETATM 177 H UNK 0 -9.549 2.702 1.286 0.00 0.00 H+0 HETATM 178 H UNK 0 -7.959 3.796 2.518 0.00 0.00 H+0 HETATM 179 H UNK 0 -6.836 2.532 2.126 0.00 0.00 H+0 HETATM 180 H UNK 0 -5.226 4.164 1.178 0.00 0.00 H+0 HETATM 181 H UNK 0 -5.642 6.636 1.438 0.00 0.00 H+0 HETATM 182 H UNK 0 -7.331 6.291 1.848 0.00 0.00 H+0 HETATM 183 H UNK 0 -6.698 5.889 0.242 0.00 0.00 H+0 HETATM 184 H UNK 0 -6.292 4.975 3.976 0.00 0.00 H+0 HETATM 185 H UNK 0 -3.574 4.025 2.919 0.00 0.00 H+0 HETATM 186 H UNK 0 -4.691 4.830 5.704 0.00 0.00 H+0 HETATM 187 H UNK 0 -3.027 5.083 5.192 0.00 0.00 H+0 HETATM 188 H UNK 0 -4.306 2.301 5.257 0.00 0.00 H+0 HETATM 189 H UNK 0 -3.639 3.028 6.716 0.00 0.00 H+0 HETATM 190 H UNK 0 -1.875 2.939 4.236 0.00 0.00 H+0 HETATM 191 H UNK 0 -0.943 0.747 5.079 0.00 0.00 H+0 HETATM 192 H UNK 0 -2.188 0.690 6.303 0.00 0.00 H+0 HETATM 193 H UNK 0 -3.692 -0.769 5.870 0.00 0.00 H+0 HETATM 194 H UNK 0 -4.808 -0.463 4.552 0.00 0.00 H+0 HETATM 195 H UNK 0 -3.930 -2.851 4.863 0.00 0.00 H+0 HETATM 196 H UNK 0 -4.957 -2.155 2.691 0.00 0.00 H+0 HETATM 197 H UNK 0 -3.375 -1.605 2.117 0.00 0.00 H+0 HETATM 198 H UNK 0 -3.759 -3.849 1.266 0.00 0.00 H+0 HETATM 199 H UNK 0 -4.123 -4.456 2.882 0.00 0.00 H+0 HETATM 200 H UNK 0 -1.808 -5.036 2.333 0.00 0.00 H+0 HETATM 201 H UNK 0 -1.469 -3.360 1.882 0.00 0.00 H+0 HETATM 202 H UNK 0 -2.109 -4.352 4.710 0.00 0.00 H+0 HETATM 203 H UNK 0 0.388 -3.188 3.377 0.00 0.00 H+0 HETATM 204 H UNK 0 0.154 -4.855 3.866 0.00 0.00 H+0 HETATM 205 H UNK 0 1.487 -3.990 5.558 0.00 0.00 H+0 HETATM 206 H UNK 0 -0.106 -4.053 6.270 0.00 0.00 H+0 HETATM 207 H UNK 0 1.135 -2.022 6.883 0.00 0.00 H+0 HETATM 208 H UNK 0 -0.376 -1.648 6.100 0.00 0.00 H+0 HETATM 209 H UNK 0 0.794 -1.069 4.001 0.00 0.00 H+0 HETATM 210 H UNK 0 1.339 -0.124 5.382 0.00 0.00 H+0 HETATM 211 H UNK 0 3.325 -1.776 5.600 0.00 0.00 H+0 HETATM 212 H UNK 0 2.760 -2.261 2.900 0.00 0.00 H+0 HETATM 213 H UNK 0 3.595 0.543 4.557 0.00 0.00 H+0 HETATM 214 H UNK 0 4.621 -0.689 3.786 0.00 0.00 H+0 HETATM 215 H UNK 0 2.321 0.568 2.825 0.00 0.00 H+0 HETATM 216 H UNK 0 0.658 3.788 6.574 0.00 0.00 H+0 HETATM 217 H UNK 0 0.094 4.043 4.914 0.00 0.00 H+0 HETATM 218 H UNK 0 0.531 2.396 5.486 0.00 0.00 H+0 HETATM 219 H UNK 0 1.613 -5.815 -3.159 0.00 0.00 H+0 HETATM 220 H UNK 0 0.275 -6.873 -3.595 0.00 0.00 H+0 HETATM 221 H UNK 0 1.332 -8.766 -2.783 0.00 0.00 H+0 HETATM 222 H UNK 0 3.674 -8.353 -2.759 0.00 0.00 H+0 HETATM 223 H UNK 0 1.331 -8.467 -0.461 0.00 0.00 H+0 HETATM 224 H UNK 0 3.337 -9.081 0.116 0.00 0.00 H+0 CONECT 1 2 99 100 CONECT 2 3 1 101 CONECT 3 4 2 102 103 CONECT 4 5 3 104 105 CONECT 5 6 4 106 CONECT 6 7 5 107 CONECT 7 8 6 108 CONECT 8 9 7 109 CONECT 9 10 8 110 CONECT 10 11 9 111 CONECT 11 12 10 112 113 CONECT 12 13 11 114 115 CONECT 13 14 12 116 CONECT 14 15 13 117 CONECT 15 17 14 16 118 CONECT 16 15 119 CONECT 17 19 15 18 120 CONECT 18 17 121 CONECT 19 20 17 97 122 CONECT 20 19 21 CONECT 21 94 20 22 123 CONECT 22 24 21 23 124 CONECT 23 22 125 CONECT 24 26 22 25 126 CONECT 25 24 127 CONECT 26 28 24 27 CONECT 27 26 128 129 CONECT 28 29 26 130 131 CONECT 29 30 28 132 133 CONECT 30 32 29 31 134 CONECT 31 30 135 CONECT 32 30 93 33 136 CONECT 33 32 34 137 138 CONECT 34 33 36 35 139 CONECT 35 34 140 CONECT 36 38 34 37 141 CONECT 37 36 142 CONECT 38 93 39 36 143 CONECT 39 41 38 40 144 CONECT 40 39 145 CONECT 41 43 39 42 146 CONECT 42 41 147 CONECT 43 44 41 148 CONECT 44 46 43 45 CONECT 45 44 149 150 151 CONECT 46 47 44 152 153 CONECT 47 48 46 49 154 CONECT 48 47 155 CONECT 49 50 47 156 157 CONECT 50 51 49 158 159 CONECT 51 52 53 50 160 CONECT 52 51 161 CONECT 53 54 51 162 163 CONECT 54 55 56 53 164 CONECT 55 54 165 CONECT 56 57 58 54 166 CONECT 57 56 167 CONECT 58 59 60 56 168 CONECT 59 58 169 170 171 CONECT 60 61 58 172 173 CONECT 61 62 63 60 174 CONECT 62 61 175 CONECT 63 64 65 61 176 CONECT 64 63 177 CONECT 65 66 63 178 179 CONECT 66 68 65 67 180 CONECT 67 66 181 182 183 CONECT 68 69 66 184 CONECT 69 70 68 185 CONECT 70 71 69 186 187 CONECT 71 72 70 188 189 CONECT 72 73 71 91 190 CONECT 73 74 72 191 192 CONECT 74 76 73 75 CONECT 75 74 CONECT 76 77 74 193 194 CONECT 77 76 90 78 195 CONECT 78 77 79 196 197 CONECT 79 78 80 198 199 CONECT 80 81 79 200 201 CONECT 81 82 90 80 202 CONECT 82 83 81 203 204 CONECT 83 84 82 205 206 CONECT 84 85 83 207 208 CONECT 85 86 84 209 210 CONECT 86 88 85 87 211 CONECT 87 86 212 CONECT 88 89 86 213 214 CONECT 89 88 215 CONECT 90 81 77 CONECT 91 72 92 CONECT 92 91 216 217 218 CONECT 93 38 32 CONECT 94 21 95 219 220 CONECT 95 94 97 96 221 CONECT 96 95 222 CONECT 97 95 19 98 223 CONECT 98 97 224 CONECT 99 1 CONECT 100 1 CONECT 101 2 CONECT 102 3 CONECT 103 3 CONECT 104 4 CONECT 105 4 CONECT 106 5 CONECT 107 6 CONECT 108 7 CONECT 109 8 CONECT 110 9 CONECT 111 10 CONECT 112 11 CONECT 113 11 CONECT 114 12 CONECT 115 12 CONECT 116 13 CONECT 117 14 CONECT 118 15 CONECT 119 16 CONECT 120 17 CONECT 121 18 CONECT 122 19 CONECT 123 21 CONECT 124 22 CONECT 125 23 CONECT 126 24 CONECT 127 25 CONECT 128 27 CONECT 129 27 CONECT 130 28 CONECT 131 28 CONECT 132 29 CONECT 133 29 CONECT 134 30 CONECT 135 31 CONECT 136 32 CONECT 137 33 CONECT 138 33 CONECT 139 34 CONECT 140 35 CONECT 141 36 CONECT 142 37 CONECT 143 38 CONECT 144 39 CONECT 145 40 CONECT 146 41 CONECT 147 42 CONECT 148 43 CONECT 149 45 CONECT 150 45 CONECT 151 45 CONECT 152 46 CONECT 153 46 CONECT 154 47 CONECT 155 48 CONECT 156 49 CONECT 157 49 CONECT 158 50 CONECT 159 50 CONECT 160 51 CONECT 161 52 CONECT 162 53 CONECT 163 53 CONECT 164 54 CONECT 165 55 CONECT 166 56 CONECT 167 57 CONECT 168 58 CONECT 169 59 CONECT 170 59 CONECT 171 59 CONECT 172 60 CONECT 173 60 CONECT 174 61 CONECT 175 62 CONECT 176 63 CONECT 177 64 CONECT 178 65 CONECT 179 65 CONECT 180 66 CONECT 181 67 CONECT 182 67 CONECT 183 67 CONECT 184 68 CONECT 185 69 CONECT 186 70 CONECT 187 70 CONECT 188 71 CONECT 189 71 CONECT 190 72 CONECT 191 73 CONECT 192 73 CONECT 193 76 CONECT 194 76 CONECT 195 77 CONECT 196 78 CONECT 197 78 CONECT 198 79 CONECT 199 79 CONECT 200 80 CONECT 201 80 CONECT 202 81 CONECT 203 82 CONECT 204 82 CONECT 205 83 CONECT 206 83 CONECT 207 84 CONECT 208 84 CONECT 209 85 CONECT 210 85 CONECT 211 86 CONECT 212 87 CONECT 213 88 CONECT 214 88 CONECT 215 89 CONECT 216 92 CONECT 217 92 CONECT 218 92 CONECT 219 94 CONECT 220 94 CONECT 221 95 CONECT 222 96 CONECT 223 97 CONECT 224 98 MASTER 0 0 0 0 0 0 0 0 224 0 452 0 END SMILES for NP0038124 (carteraol E)[H]OC([H])([H])[C@]([H])(O[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])O[C@@]([H])(C([H])([H])C(=O)C([H])([H])[C@]([H])(OC([H])([H])[H])C([H])([H])C([H])([H])C(\[H])=C(/[H])[C@]([H])(C([H])([H])[H])C([H])([H])[C@]([H])(O[H])[C@]([H])(O[H])C([H])([H])[C@@]([H])(C([H])([H])[H])[C@@]([H])(O[H])[C@]([H])(O[H])C([H])([H])[C@]([H])(O[H])C([H])([H])C([H])([H])[C@@]([H])(O[H])C([H])([H])C(=C(/[H])[C@@]([H])(O[H])[C@@]([H])(O[H])[C@@]2([H])O[C@]([H])(C([H])([H])[C@@]([H])(O[H])[C@@]2([H])O[H])[C@@]([H])(O[H])C([H])([H])C([H])([H])C(=C([H])[H])[C@@]([H])(O[H])[C@]([H])(O[H])[C@]2([H])O[C@@]([H])([C@]([H])(O[H])[C@@]([H])(O[H])C(\[H])=C(/[H])C([H])([H])C([H])([H])C(\[H])=C(/[H])\C(\[H])=C(/[H])\C(\[H])=C(/[H])C([H])([H])C([H])([H])C([H])=C([H])[H])[C@]([H])(O[H])[C@]([H])(O[H])C2([H])[H])\C([H])([H])[H])C([H])([H])C([H])([H])C1([H])[H] INCHI for NP0038124 (carteraol E)InChI=1S/C74H126O24/c1-7-8-9-10-11-12-13-14-15-16-17-18-30-57(81)68(90)73-71(93)63(87)43-65(98-73)72(94)67(89)47(4)31-34-56(80)64-42-62(86)70(92)74(97-64)69(91)60(84)37-46(3)35-49(76)32-33-50(77)41-61(85)66(88)48(5)38-59(83)58(82)36-45(2)24-19-21-27-54(95-6)39-52(79)40-55-29-23-28-53(96-55)26-22-20-25-51(78)44-75/h7,10-15,18-19,24,30,37,45,48-51,53-78,80-94H,1,4,8-9,16-17,20-23,25-29,31-36,38-44H2,2-3,5-6H3/b11-10+,13-12+,15-14+,24-19+,30-18+,46-37+/t45-,48+,49+,50+,51+,53+,54+,55+,56-,57-,58-,59+,60+,61+,62+,63+,64+,65+,66+,67+,68+,69+,70+,71+,72+,73-,74+/m0/s1 3D Structure for NP0038124 (carteraol E) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Synonyms | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Chemical Formula | C74H126O24 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Average Mass | 1399.7980 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Monoisotopic Mass | 1398.86390 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| IUPAC Name | (4R,7E,9R,11S,12R,14R,15R,16R,18R,21R,23E,25R,26R)-26-[(2S,3R,4R,6R)-6-[(1S,5R,6S)-6-[(2R,4R,5R,6R)-6-[(1R,2S,3E,7E,9E,11E)-1,2-dihydroxyhexadeca-3,7,9,11,15-pentaen-1-yl]-4,5-dihydroxyoxan-2-yl]-1,5,6-trihydroxy-4-methylidenehexyl]-3,4-dihydroxyoxan-2-yl]-1-[(2R,6R)-6-[(5R)-5,6-dihydroxyhexyl]oxan-2-yl]-11,12,15,16,18,21,25,26-octahydroxy-4-methoxy-9,14,23-trimethylhexacosa-7,23-dien-2-one | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Traditional Name | (4R,7E,9R,11S,12R,14R,15R,16R,18R,21R,23E,25R,26R)-26-[(2S,3R,4R,6R)-6-[(1S,5R,6S)-6-[(2R,4R,5R,6R)-6-[(1R,2S,3E,7E,9E,11E)-1,2-dihydroxyhexadeca-3,7,9,11,15-pentaen-1-yl]-4,5-dihydroxyoxan-2-yl]-1,5,6-trihydroxy-4-methylidenehexyl]-3,4-dihydroxyoxan-2-yl]-1-[(2R,6R)-6-[(5R)-5,6-dihydroxyhexyl]oxan-2-yl]-11,12,15,16,18,21,25,26-octahydroxy-4-methoxy-9,14,23-trimethylhexacosa-7,23-dien-2-one | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| SMILES | [H]OC([H])([H])[C@]([H])(O[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])O[C@@]([H])(C([H])([H])C(=O)C([H])([H])[C@]([H])(OC([H])([H])[H])C([H])([H])C([H])([H])C(\[H])=C(/[H])[C@]([H])(C([H])([H])[H])C([H])([H])[C@]([H])(O[H])[C@]([H])(O[H])C([H])([H])[C@@]([H])(C([H])([H])[H])[C@@]([H])(O[H])[C@]([H])(O[H])C([H])([H])[C@]([H])(O[H])C([H])([H])C([H])([H])[C@@]([H])(O[H])C([H])([H])C(=C(/[H])[C@@]([H])(O[H])[C@@]([H])(O[H])[C@@]2([H])O[C@]([H])(C([H])([H])[C@@]([H])(O[H])[C@@]2([H])O[H])[C@@]([H])(O[H])C([H])([H])C([H])([H])C(=C([H])[H])[C@@]([H])(O[H])[C@]([H])(O[H])[C@]2([H])O[C@@]([H])([C@]([H])(O[H])[C@@]([H])(O[H])C(\[H])=C(/[H])C([H])([H])C([H])([H])C(\[H])=C(/[H])\C(\[H])=C(/[H])\C(\[H])=C(/[H])C([H])([H])C([H])([H])C([H])=C([H])[H])[C@]([H])(O[H])[C@]([H])(O[H])C2([H])[H])\C([H])([H])[H])C([H])([H])C([H])([H])C1([H])[H] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Identifier | InChI=1S/C74H126O24/c1-7-8-9-10-11-12-13-14-15-16-17-18-30-57(81)68(90)73-71(93)63(87)43-65(98-73)72(94)67(89)47(4)31-34-56(80)64-42-62(86)70(92)74(97-64)69(91)60(84)37-46(3)35-49(76)32-33-50(77)41-61(85)66(88)48(5)38-59(83)58(82)36-45(2)24-19-21-27-54(95-6)39-52(79)40-55-29-23-28-53(96-55)26-22-20-25-51(78)44-75/h7,10-15,18-19,24,30,37,45,48-51,53-78,80-94H,1,4,8-9,16-17,20-23,25-29,31-36,38-44H2,2-3,5-6H3/b11-10+,13-12+,15-14+,24-19+,30-18+,46-37+/t45-,48+,49+,50+,51+,53+,54+,55+,56-,57-,58-,59+,60+,61+,62+,63+,64+,65+,66+,67+,68+,69+,70+,71+,72+,73-,74+/m0/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| InChI Key | FMPBABOEFWIINO-DMQQLDSRSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Experimental Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Predicted Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| External Links | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| References | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| General References |
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