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Compounds

COMPOUND NPA021255

STRUCTURE

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PROJECT MOLECULE TO GLOBAL VIEW	See Global

EXTERNAL LINKS

PROPERTIES

NPAID	NPA021255
CLUSTER ID	217
NODE ID	204
NAME	30-di-(O-methyl)actamycin25
FORMULA	C41H49NO10
MOLECULAR WEIGHT (Da)	715.8400
ACCURATE MASS (Da)	715.3356
ORIGIN ORGANISM TYPE	Bacterium
ORIGIN GENUS	Streptomyces
ORIGIN SPECIES	sp. E/784
InChIKey	AWDFLSTVICEQJQ-AWYKWAPWSA-N
InChI	InChI=1S/C41H49NO10/c1-21-12-10-9-11-13-24(4)41(51)42-34-38(49)29-19-27(7)37(48)33(32(29)39(50)40(34)52-8)36(47)26(6)18-25(5)35(46)23(3)15-17-28(43)16-14-22(2)31(45)20-30(21)44/h9-15,17-19,21,23,25,28,30,35,43-44,46,48H,16,20H2,1-8H3,(H,42,51)/b11-9-,12-10+,17-15+,22-14+,24-13-,26-18+/t21-,23-,25-,28-,30-,35-/m0/s1
SMILES	C[C@H]1/C=C/C=C\C=C(/C(=O)NC2=C(C(=O)C3=C(C(=C(C=C3C2=O)C)O)C(=O)/C(=C/[C@@H]([C@H]([C@H](/C=C/[C@H](C/C=C(/C(=O)C[C@@H]1O)\C)O)C)O)C)/C)OC)\C

ORIGINAL ISOLATION REFERENCE

CITATION	Hooper AM; Rickards RW 3-Amino-5-hydroxybenzoic Acid in Antibiotic Biosynthesis Journal of Antibiotics 1998 51 (10) 958-962.
DOI	10.7164/antibiotics.51.958	PMID	9917011

ORIGINAL ISOLATION TAXONOMY

RANK	NAME	DB LINK	NCBI
Domain	Bacteria	LPSN	2
Phylum	Actinobacteria	LPSN	201174
Class	Actinobacteria	LPSN	-
Order	Streptomycetales	LPSN	85011
Family	Streptomycetaceae	LPSN	2062
Genus	Streptomyces	LPSN	1883

CLASSYFIRE

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DESCRIPTION	[[ getValue('description') ]]
KINGDOM	[[ getValue('kingdom') ]]
SUPER CLASS	[[ getValue('superclass') ]]
CLASS	[[ getValue('class') ]]
SUB CLASS	[[ getValue('subclass') ]]
MOLECULAR FRAMEWORK	[[ getValue('molecular_framework') ]]

NP CLASSIFIER

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SUPER CLASS	[[ getValue('superclass_results') ]]
CLASS	[[ getValue('class_results') ]]
PATHWAY	[[ getValue('pathway_results') ]]
IS GLYCOSIDE?	[[ getValue('isglycoside') ]]

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