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Compounds

COMPOUND NPA007949

STRUCTURE

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PROPERTIES

NPAID	NPA007949
CLUSTER ID	46
NODE ID	11
NAME	Saquayamycin J
FORMULA	C43H52O16
MOLECULAR WEIGHT (Da)	824.8730
ACCURATE MASS (Da)	824.3255
ORIGIN ORGANISM TYPE	Bacterium
ORIGIN GENUS	Streptomyces
ORIGIN SPECIES	sp. KY40-1
InChIKey	CVLVPRNGMHOWPC-QEBONLAISA-N
InChI	InChI=1S/C43H52O16/c1-18-25(44)8-10-32(53-18)57-27-9-11-33(54-20(27)3)59-41(5)16-31(46)43(51)35-24(12-13-42(43,50)17-41)37(48)34-23(38(35)49)7-6-22(36(34)47)28-15-29-39(21(4)52-28)58-40-30(56-29)14-26(45)19(2)55-40/h6-7,12-13,18-21,25,27-30,32-33,39-40,44,47,50-51H,8-11,14-17H2,1-5H3/t18-,19-,20-,21+,25-,27-,28+,29+,30-,32-,33-,39+,40-,41-,42-,43-/m0/s1
SMILES	C[C@H]1[C@H](CC[C@@H](O1)O[C@H]2CC[C@@H](O[C@H]2C)O[C@]3(CC(=O)[C@@]4(C5=C(C=C[C@@]4(C3)O)C(=O)C6=C(C5=O)C=CC(=C6O)[C@H]7C[C@@H]8[C@@H]([C@H](O7)C)O[C@H]9[C@@H](O8)CC(=O)[C@@H](O9)C)O)C)O

ORIGINAL ISOLATION REFERENCE

CITATION	Shaaban, Khaled A.; Ahmed, Tamer A.; Leggas, Markos; Rohr, Juergen Saquayamycins G-K, cytotoxic angucyclines from streptomyces sp. including two analogues bearing the aminosugar rednose Journal of Natural Products 2012 75 (7) 1383-1392.
DOI	10.1021/np300316b	PMID	22758660

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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