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Compounds

COMPOUND NPA014173

STRUCTURE

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PROPERTIES

NPAID	NPA014173
CLUSTER ID	664
NODE ID	590
NAME	(3Z,5E,7R,8S,9R,11E,13E,15S,16R)-16-{(2S,3E)-4-[(2R)-2-ethyl-3-methyl-2H-pyran-6-yl]-3-penten-2-yl}-8-hydroxy-3,15-dimethoxy-5,7,9,11-tetramethyloxacyclohexadeca-3,5,11,13-tetraen-2-one
FORMULA	C34H50O6
MOLECULAR WEIGHT (Da)	554.7680
ACCURATE MASS (Da)	554.3607
ORIGIN ORGANISM TYPE	Bacterium
ORIGIN GENUS	Streptomyces
ORIGIN SPECIES	sp. CS
InChIKey	JXMOXMDSHOTTME-SWDJTEKNSA-N
InChI	InChI=1S/C34H50O6/c1-11-28-23(4)15-16-29(39-28)24(5)20-27(8)33-30(37-9)14-12-13-21(2)17-25(6)32(35)26(7)18-22(3)19-31(38-10)34(36)40-33/h12-16,18-20,25-28,30,32-33,35H,11,17H2,1-10H3/b14-12-,21-13-,22-18-,24-20+,31-19+/t25-,26+,27-,28+,30-,32-,33+/m0/s1
SMILES	CC[C@@H]1C(=CC=C(O1)/C(=C/[C@H](C)[C@@H]2[C@H](/C=C\C=C(/C[C@@H]([C@@H]([C@@H](/C=C(\C=C(/C(=O)O2)\OC)/C)C)O)C)\C)OC)/C)C

ORIGINAL ISOLATION REFERENCE

CITATION	Lu, Chunhua; Shen, Yuemao Two new macrolides produced by Streptomyces sp. CS Journal of Antibiotics 2004 57 (9) 597.
DOI	10.7164/antibiotics.57.597	PMID	15580961

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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