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Compounds

COMPOUND NPA008281

STRUCTURE

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PROPERTIES

NPAID	NPA008281
CLUSTER ID	3563
NODE ID	2683
NAME	Cruentaren B
FORMULA	C33H51NO8
MOLECULAR WEIGHT (Da)	589.7700
ACCURATE MASS (Da)	589.3615
ORIGIN ORGANISM TYPE	Bacterium
ORIGIN GENUS	Byssovorax
ORIGIN SPECIES	cruenta
InChIKey	MXMBYAYSVKOAKI-XESWYYRISA-N
InChI	InChI=1S/C33H51NO8/c1-7-12-26(35)23(5)32(39)34-16-11-10-14-21(3)31(38)22(4)27(36)15-9-8-13-20(2)29-18-24-17-25(41-6)19-28(37)30(24)33(40)42-29/h8-11,17,19-23,26-27,29,31,35-38H,7,12-16,18H2,1-6H3,(H,34,39)/b9-8-,11-10-
SMILES	CCCC(C(C)C(=O)NC/C=C\CC(C)C(C(C)C(C/C=C\CC(C)C1CC2=CC(=CC(=C2C(=O)O1)O)OC)O)O)O

ORIGINAL ISOLATION REFERENCE

CITATION	Kunze, Brigitte; Steinmetz, Heinrich; Hoefle, Gerhard; Huss, Markus; Wieczorek, Helmut; Reichenbach, Hans Cruentaren, a new antifungal salicylate-type macrolide from Byssovorax cruenta (Myxobacteria) with inhibitory effect on mitochondrial ATPase activity: Fermentation and biological properties Journal of Antibiotics 2006 59 (10) 664-668.
DOI	10.1038/ja.2006.89	PMID	17191683

ORIGINAL ISOLATION TAXONOMY

RANK	NAME	DB LINK	NCBI
Domain	Bacteria	LPSN	2
Phylum	Proteobacteria	LPSN	1224
Class	Deltaproteobacteria	LPSN	28221
Order	Myxococcales	LPSN	29
Family	Polyangiaceae	LPSN	49
Genus	Byssovorax	LPSN	224459

SYNTHESES

CITATION 1	Chakraborty TK; Chattopadhyay AK Total synthesis of cruentaren B. Journal of Organic Chemistry 2008 73 (9) 3578-3581. DOI: 10.1021/jo800181n PMID: 18363370

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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