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Compounds

COMPOUND NPA011436

STRUCTURE

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PROPERTIES

NPAID	NPA011436
CLUSTER ID	1049
NODE ID	904
NAME	Pamamycin 621A
FORMULA	C36H63NO7
MOLECULAR WEIGHT (Da)	621.9000
ACCURATE MASS (Da)	621.4605
ORIGIN ORGANISM TYPE	Bacterium
ORIGIN GENUS	Streptomyces
ORIGIN SPECIES	alboniger IFO 12738
InChIKey	MMFMMXXZYTWNGM-ZZSWZHNPSA-N
InChI	InChI=1S/C36H63NO7/c1-10-12-26(37(8)9)20-27-14-15-30(40-27)22(4)34-23(5)31-17-19-32(42-31)24(6)35(38)43-28(13-11-2)21(3)29-16-18-33(41-29)25(7)36(39)44-34/h21-34H,10-20H2,1-9H3/t21-,22+,23+,24+,25-,26+,27-,28-,29-,30+,31-,32+,33+,34-/m0/s1
SMILES	CCC[C@H]1[C@@H]([C@@H]2CC[C@@H](O2)[C@@H](C(=O)O[C@H]([C@@H]([C@@H]3CC[C@@H](O3)[C@H](C(=O)O1)C)C)[C@H](C)[C@H]4CC[C@H](O4)C[C@@H](CCC)N(C)C)C)C

ORIGINAL ISOLATION REFERENCE

CITATION	Natsume; Tazawa; Yagi; Abe; Kondo; Marumo Structure-activity relationship of pamamycins: Effects of alkyl substituents Journal of Antibiotics 1995 48 (10) 1159-1164.
DOI	10.7164/antibiotics.48.1159	PMID	7490225

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

SYNTHESES

CITATION 1	Ren GB; Huang YX; Sun YP; Li ZH; Wu Y An enantioselective convergent route to pamamycin 621A. Journal of Organic Chemistry 2010 75 (15) 5048-5064. DOI: 10.1021/jo100774n PMID: 20597495

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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