(Q105347765)

English

[(3S)-10-hydroxy-1-methyl-9-oxo-3H,4H-naphtho[2,3-c]pyran-3-yl]acetic acid

chemical compound

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No description defined

Statements

type of chemical entity

0 references

chemical compound

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286.084123548 dalton

1 reference

based on heuristic

inferred from SMILES

chemical formula

C₁₆H₁₄O₅

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canonical SMILES

O=C(O)CC1OC(=C2C(O)=C3C(=O)C=CC=C3C=C2C1)C

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isomeric SMILES

CC1=c2c(cc3c(c2O)C(=O)C=CC=3)C[C@@H](CC(=O)O)O1

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Streptomyces albidoflavus

2 references

Chemical Characterisation of Disruptants of the Streptomyces coelicolor A3(2). ActVI Genes Involved in Actinorhodin Biosynthesis.

A new mode of stereochemical control revealed by analysis of the biosynthesis of dihydrogranaticin in Streptomyces violaceoruber Tü22.

Streptomyces coelicolor

2 references

Chemical Characterisation of Disruptants of the Streptomyces coelicolor A3(2). ActVI Genes Involved in Actinorhodin Biosynthesis.

A new mode of stereochemical control revealed by analysis of the biosynthesis of dihydrogranaticin in Streptomyces violaceoruber Tü22.

Streptomyces violaceoruber

2 references

Chemical Characterisation of Disruptants of the Streptomyces coelicolor A3(2). ActVI Genes Involved in Actinorhodin Biosynthesis.

A new mode of stereochemical control revealed by analysis of the biosynthesis of dihydrogranaticin in Streptomyces violaceoruber Tü22.

Identifiers

InChI=1S/C16H14O5/c1-8-14-10(6-11(21-8)7-13(18)19)5-9-3-2-4-12(17)15(9)16(14)20/h2-5,11,20H,6-7H2,1H3,(H,18,19)/t11-/m0/s1

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YFRUSKASGPDFBR-NSHDSACASA-N

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1 reference

17 September 2022

based on heuristic

inferred from InChIKey

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