Compounds
ID | Spectrum Quality | Annotated Name |
---|
COMPOUND NPA017600
PROPERTIES
NPAID | NPA017600 |
---|---|
CLUSTER ID | 1662 |
NODE ID | 1358 |
NAME | Durhamycin B |
FORMULA | C56H82O25 |
MOLECULAR WEIGHT (Da) | 1155.2470 |
ACCURATE MASS (Da) | 1154.5145 |
ORIGIN ORGANISM TYPE | Bacterium |
ORIGIN GENUS | Actinoplanes |
ORIGIN SPECIES | durhamensis |
InChIKey | ICFBIVXFINBMRC-DBYMNNJYSA-N |
InChI | InChI=1S/C56H82O25/c1-11-20(2)42-33(77-39-17-34(48(64)24(6)73-39)78-37-15-31(59)46(62)22(4)71-37)14-29-12-28-13-30(55(70-10)53(69)45(61)21(3)57)56(52(68)44(28)51(67)43(29)50(42)66)81-41-18-35(49(65)25(7)74-41)79-40-19-36(54(26(8)75-40)76-27(9)58)80-38-16-32(60)47(63)23(5)72-38/h12,14,20-26,30-32,34-41,45-49,54-57,59-67H,11,13,15-19H2,1-10H3/t20?,21?,22-,23-,24-,25-,26-,30?,31-,32-,34-,35-,36-,37+,38+,39+,40+,41+,45?,46-,47-,48-,49-,54+,55?,56?/m1/s1 |
SMILES | CCC(C)C1=C(C2=C(C3=C(CC(C(C3=O)O[C@H]4C[C@H]([C@@H]([C@H](O4)C)O)O[C@H]5C[C@H]([C@H]([C@H](O5)C)OC(=O)C)O[C@H]6C[C@H]([C@@H]([C@H](O6)C)O)O)C(C(=O)C(C(C)O)O)OC)C=C2C=C1O[C@H]7C[C@H]([C@@H]([C@H](O7)C)O)O[C@H]8C[C@H]([C@@H]([C@H](O8)C)O)O)O)O |
ORIGINAL ISOLATION REFERENCE
CITATION | Jayasuriya, Hiranthi; Lingham, Russell B; Graham, Pia; Quamina, Donette; Herranz, Lucia; Genilloud, Olga; Gagliardi, Magda; Danzeisen, Renee; Tomassini, Joanne E; Zink, Deborah L; Guan, Ziqiang; Singh, Sheo B Durhamycin A, a potent inhibitor of HIV Tat transactivation Journal of Natural Products 2002 65 (8) 1091-1095. | ||
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DOI | 10.3410/f.1003977.152960 | PMID | 12193009 |