(Q82881657)

English

Olivoretin E

chemical compound

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Statements

type of chemical entity

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indolactam alkaloid

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465.335527616 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₂₉H₄₃N₃O₂

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canonical SMILES

C=CC1(C)CCC(C(C)(C)C)c2c1cc1c3c(c[nH]c23)CC(COC)NC(=O)C(C(C)C)N1C

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isomeric SMILES

CC(C)[C@H]1C(=O)N[C@@H](CC2=CNC3=C4[C@H](CC[C@](C4=CC(=C23)N1C)(C)C=C)C(C)(C)C)COC

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Streptomyces blastmyceticus

1 reference

Biosynthesis of indole alkaloid tumor promoters teleocidins (I) possible biosynthetic pathway of the monoterpenoid moieties of teleocidins

Streptomyces abikoensis

1 reference

The structures of additional teleocidin class tumor promoters

Identifiers

InChI=1S/C29H43N3O2/c1-10-29(7)12-11-20(28(4,5)6)24-21(29)14-22-23-18(15-30-25(23)24)13-19(16-34-9)31-27(33)26(17(2)3)32(22)8/h10,14-15,17,19-20,26,30H,1,11-13,16H2,2-9H3,(H,31,33)/t19-,20-,26-,29-/m0/s1

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XVXFTYXRGYNKBI-JKRNNPMPSA-N

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CAS Registry Number

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1 reference

matched by identifier from

XVXFTYXRGYNKBI-JKRNNPMPSA-N

mapping relation type

1 reference

matched by identifier from

International Chemical Identifier

InChI=1S/C29H43N3O2/c1-10-29(7)12-11-20(28(4,5)6)24-21(29)14-22-23-18(15-30-25(23)24)13-19(16-34-9)31-27(33)26(17(2)3)32(22)8/h10,14-15,17,19-20,26,30H,1,11-13,16H2,2-9H3,(H,31,33)/t19-,20-,26-,29-/m0/s1

UniChem compound ID

1 reference

DSSTox substance ID

1 reference

matched by identifier from

XVXFTYXRGYNKBI-JKRNNPMPSA-N

DSSTOX compound identifier

DTXCID501340553

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Natural Product Atlas ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

XVXFTYXRGYNKBI-JKRNNPMPSA-N

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