Natural Products Atlas | Compounds

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Compounds

ID	Spectrum Quality	Annotated Name
CCMSLIB00004712449	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712450	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712451	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712452	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712453	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712454	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712455	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712456	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712457	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712448	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712459	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712460	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712461	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712462	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00004712458	Bronze	4-hydroxy-5-[2-[(E)-3-hydroxyprop-1-enyl]-4-methylphenyl]-3-methylhexan-2-one
CCMSLIB00000848552	Gold	1
CCMSLIB00005721888	Gold	3
CCMSLIB00005721889	Gold	3

COMPOUND NPA002050

STRUCTURE

Image structure

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PROJECT MOLECULE TO GLOBAL VIEW	See Global

EXTERNAL LINKS

PROPERTIES

NPAID	NPA002050
CLUSTER ID	1265
NODE ID	1072
NAME	NFAT-133
FORMULA	C17H24O3
MOLECULAR WEIGHT (Da)	276.3760
ACCURATE MASS (Da)	276.1725
ORIGIN ORGANISM TYPE	Bacterium
ORIGIN GENUS	Streptomyces
ORIGIN SPECIES	sp.
InChIKey	FTTQBBNJVTYJPS-AATRIKPKSA-N
InChI	InChI=1S/C17H24O3/c1-11-7-8-16(15(10-11)6-5-9-18)13(3)17(20)12(2)14(4)19/h5-8,10,12-13,17-18,20H,9H2,1-4H3/b6-5+
SMILES	CC1=CC(=C(C=C1)C(C)C(C(C)C(=O)C)O)/C=C/CO

ORIGINAL ISOLATION REFERENCE

CITATION	Burres; Premachandran; Hoselton; Cwik; Hochlowski; Ye; Sunga; Karwowski; Jackson; Whittern; McAlpine Simple aromatics identified with a NFAT-lacZ transcription assay for the detection of immunosuppressants Journal of Antibiotics 1995 48 (5) 380-386.
DOI	10.7164/antibiotics.48.380	PMID	7797439

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	Sato H; Kwon E; Taguchi Y; Yoshida S; Kuwahara S; Ogura Y Synthesis and Stereochemical Revision of the Aromatic Polyketide NFAT-133. Journal of Natural Products 2019 82 (7) 1791-1796. DOI: 10.1021/acs.jnatprod.8b01063 PMID: 31268714

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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