Compounds
ID | Spectrum Quality | Annotated Name |
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COMPOUND NPA002249
PROPERTIES
NPAID | NPA002249 |
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CLUSTER ID | 1354 |
NODE ID | 1138 |
NAME | Tautomycetin |
FORMULA | C33H50O10 |
MOLECULAR WEIGHT (Da) | 606.7530 |
ACCURATE MASS (Da) | 606.3404 |
ORIGIN ORGANISM TYPE | Bacterium |
ORIGIN GENUS | Streptomyces |
ORIGIN SPECIES | griseochromogenes |
InChIKey | VAIBGAONSFVVKI-LOIRJACGSA-N |
InChI | InChI=1S/C33H50O10/c1-9-24(10-2)15-25(34)14-19(4)13-18(3)11-12-26(35)21(6)28(37)16-27(36)20(5)23(8)42-30(39)17-29(38)31-22(7)32(40)43-33(31)41/h9,15,18-21,23,26-27,29,35-36,38H,1,10-14,16-17H2,2-8H3/b24-15-/t18?,19?,20?,21?,23?,26?,27?,29-/m1/s1 |
SMILES | CC/C(=C\C(=O)CC(C)CC(C)CCC(C(C)C(=O)CC(C(C)C(C)OC(=O)C[C@H](C1=C(C(=O)OC1=O)C)O)O)O)/C=C |
ORIGINAL ISOLATION REFERENCE
CITATION | CHENG, XING-CHUN; UBUKATA, MAKOTO; ISONO, KIYOSHI; 1990, ; tautomycetin, 'The structure of; antibiotic.', a dialkylmaleic anhydride; Antibiotics</i>, <i>The Journal of; 43, vol.; 7, no.; 890-896, pp. The structure of tautomycetin, a dialkylmaleic anhydride antibiotic Journal of Antibiotics 1989 43 (7) 890-896. | ||
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DOI | 10.7164/antibiotics.43.890 | PMID | 2387780 |
SYNTHESES
CITATION 1 | Oikawa H Synthesis of specific protein phosphatase inhibitors, tautomycin and tautomycetin toward structure-activity relationship study. Current Medicinal Chemistry 2002 9 (22) 2033-53. DOI: 10.2174/0929867023368818 PMID: 12369869 |
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