4-[2-(2-amino-2-oxoethyl)-2,7-dihydroxy-4-oxochroman-5-yl]-3-hydroxybut-2-enoic acid (Q43394722)

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group of stereoisomers

• 4-(2-carbamoyl-2,7-dihydroxy-4- oxo-chroman-5-yl)-3-hydroxy-but-2-enoic acid
• LH-4

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Language	Label	Description	Also known as
English	4-[2-(2-amino-2-oxoethyl)-2,7-dihydroxy-4-oxochroman-5-yl]-3-hydroxybut-2-enoic acid	group of stereoisomers	4-(2-carbamoyl-2,7-dihydroxy-4- oxo-chroman-5-yl)-3-hydroxy-but-2-enoic acid LH-4

Statements

instance of

group of stereoisomers

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subclass of

chemical compound

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chemical structure

LH-4 structure.svg
398 × 233; 17 KB

media legend

struktura LH-4 bez wskazanej stereochemii cząsteczki (Polish)

structure of LH-4 with undefined stereochemistry (English)

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mass

337.07976644 dalton

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based on heuristic

inferred from isomeric SMILES

chemical formula

C₁₅H₁₅NO₈

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canonical SMILES

O=C(N)CC1(O)CC(C2=C(O1)C=C(O)C=C2CC(O)=CC(O)=O)=O

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isomeric SMILES

NC(=O)CC1(O)CC(=O)c2c(C/C(O)=C/C(=O)O)cc(O)cc2O1

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described by source

Disruption of an aromatase/cyclase from the oxytetracycline gene cluster of Streptomyces rimosus results in production of novel polyketides with shorter chain lengths.

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Identifiers

InChI

InChI=1S/C15H15NO8/c16-12(20)6-15(23)5-10(19)14-7(2-9(18)4-13(21)22)1-8(17)3-11(14)24-15/h1,3-4,17-18,23H,2,5-6H2,(H2,16,20)(H,21,22)/b9-4-

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InChIKey

QDABZIRVKNHPLW-WTKPLQERSA-N

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CAS Registry Number

254733-00-1

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