(Q104984816)

English

streptonigrin

chemical compound

In more languages

Statements

type of chemical entity

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quinoline alkaloid

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506.143763664 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₂₅H₂₂N₄O₈

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canonical SMILES

O=C(O)C=1NC(C=2N=C3C(=O)C(N)=C(OC)C(=O)C3=CC2)=C(N)C(=C4C=CC(OC)=C(OC)C4=O)C1C

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isomeric SMILES

COC1=C(OC)C(=O)/C(=C2/C(C)=C(C(=O)O)NC(c3ccc4c(n3)C(=O)C(N)=C(OC)C4=O)=C2N)C=C1

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Streptomyces flocculus

5 references

Ammonium effects on streptonigrin biosynthesis by Streptomyces flocculus

A tryptophan C-methyltransferase involved in streptonigrin biosynthesis in Streptomyces flocculus

Streptonigrin biosynthesis. 2. The isolation of β-methyltryptophan and its intermediacy in the streptonigrin pathway

Streptonigrin biosynthesis. 8. Evidence for the involvement of a new shikimate pathway product and a new route to quinolines

S-adenosylhomocysteine metabolism in Streptomyces flocculus

2 references

Biological properties of streptonigrin derivatives. I. Antimicrobial and cytocidal activities

The structure of streptonigrone, and a comment on the biosynthesis of the streptonigrin antibiotics.

Streptomyces albus

5 references

Streptonigrin biosynthesis. 2. The isolation of β-methyltryptophan and its intermediacy in the streptonigrin pathway

Ammonium effects on streptonigrin biosynthesis by Streptomyces flocculus

A tryptophan C-methyltransferase involved in streptonigrin biosynthesis in Streptomyces flocculus

S-adenosylhomocysteine metabolism in Streptomyces flocculus

Streptonigrin biosynthesis. 8. Evidence for the involvement of a new shikimate pathway product and a new route to quinolines

Identifiers

InChI=1S/C25H22N4O8/c1-9-14(10-6-8-13(35-2)23(36-3)20(10)30)15(26)19(29-17(9)25(33)34)12-7-5-11-18(28-12)22(32)16(27)24(37-4)21(11)31/h5-8,29H,26-27H2,1-4H3,(H,33,34)/b14-10-

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DLWOTOMWYCRPLK-UVTDQMKNSA-N

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1 reference

17 September 2022

based on heuristic

inferred from InChIKey

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

DLWOTOMWYCRPLK-UVTDQMKNSA-N

Probes And Drugs ID

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