streptonigrin

Metabolite details

Identifier

PVYJZLYGTZKPJE-UHFFFAOYSA-N

InChI Key

PVYJZLYGTZKPJE-UHFFFAOYSA-N

IUPAC name

5-amino-6-(7-amino-6-methoxy-5,8-dioxo-5,8-dihydroquinolin-2-yl)-4-(2-hydroxy-3,4-dimethoxyphenyl)-3-methylpyridine-2-carboxylic acid

Preferred name

streptonigrin

INN name

rufocromomycin

Synonym

5-Amino-6-(7-amino-5,8-dihydro-6-methoxy-5,8-dioxo-2-quinolyl)-4-(2-hydroxy-3,4-dimethoxyphenyl)-3-methylpicolinic acid

ChEBI

CHEBI:9287

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• Transcriptomics and metabolomics of engineered Synechococcus elongatus during photomixotrophic growth
• Metabolic profilings of rat INS-1 β-cells under changing levels of essential amino acids
• Unraveling the metabolic effects of benzophenone-3 on the endosymbiotic dinoflagellate Cladocopium goreaui
• L-leucine increases the sensitivity of drug-resistant Salmonella to sarafloxacin by stimulating central carbon metabolism and increasing intracellular reactive oxygen species level (LC-MS positive mode)

Observed in differential profiles

• Wild_Type_vs_YQ2-gal
• Wild_Type_vs_YQ2-gal
• G1_Control_vs_G2_Arginine_Addition
• Control_vs_BP3_Low_Concentration
• SAR-S_vs_SAR-R