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1013-69-0,MFCD03001435
Catalog No.:AA000443
1013-69-0 | Noreugenin
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  • Technical Information
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Technical Information
Catalog Number:
AA000443
Chemical Name:
Noreugenin
CAS Number:
1013-69-0
Molecular Formula:
C10H8O4
Molecular Weight:
192.1681
MDL Number:
MFCD03001435
IUPAC Name:
5,7-dihydroxy-2-methylchromen-4-one
InChI:
InChI=1S/C10H8O4/c1-5-2-7(12)10-8(13)3-6(11)4-9(10)14-5/h2-4,11,13H,1H3
InChI Key:
NCUJRUDLFCGVOE-UHFFFAOYSA-N
SMILES:
Oc1cc(O)c2c(c1)oc(cc2=O)C
UNII:
M0KFC1Q5JC
Properties
Computed Properties
 
Complexity:
284  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
192.042g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
192.17g/mol
Monoisotopic Mass:
192.042g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
66.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.8  

Synonyms
 
Noreugenin 
1013-69-0 
CHEBI:67375 
NCUJRUDLFCGVOE-UHFFFAOYSA-N 
Chromone, 5,7-dihydroxy-2-methyl- 
AC1NT9FP 
SCHEMBL168822 
2-Methyl-5,7-dihydroxychromon 
CHEMBL507707 
5,7-Dihydroxy-2-methylchromome 
DTXSID80143828 
ZINC5765136 
5,7-Dihydroxy-2-methyl-4H-chromen-4-one 
MFCD03001435 
AKOS006277487 
5,7-dihydroxy-2-methyl-chromen-4-one 
4CN-1509 
W2044 
5,7-Dihydroxy-2-methyl-4H-chromen-4-one # 
C20462 
4H-1-Benzopyran-4-one,5,7-dihydroxy-2-methyl- 
C10H8O4 
AIDS051921 
5,7-Dihydroxy-2-methylchromone 
C10-H8-O4 
ACN-057338 
CID5375252 
UNII-M0KFC1Q5JC 
5,7-Dihydroxy-2-methyl-4H-1-benzopyran-4-one 
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-methyl- 
M0KFC1Q5JC 
5,7-dihydroxy-2-methylchromen-4-one 
2-Methyl-5,7-dihydroxychromone 
Literature

Title: Antitubercular chromones and flavonoids from Pisonia aculeata.

Journal: Journal of natural products 20110527

Title: Ceramide and Cerebroside from the stem bark of Ficus mucuso (Moraceae).

Journal: Chemical & pharmaceutical bulletin 20101201

Title: Engineered biosynthesis of plant polyketides: structure-based and precursor-directed approach.

Journal: Topics in current chemistry 20100101

Title: Chrotacumines A-D, chromone alkaloids from Dysoxylum acutangulum.

Journal: Journal of natural products 20091001

Title: Cytotoxic and HIF-1alpha inhibitory compounds from Crossosoma bigelovii.

Journal: Journal of natural products 20090522

Title: [Study on chemical constituents from roots of Saussurea lappa].

Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20090501

Title: Structure-based engineering of a plant type III polyketide synthase: formation of an unnatural nonaketide naphthopyrone.

Journal: Journal of the American Chemical Society 20070509

Title: Crystallization and preliminary crystallographic analysis of a novel plant type III polyketide synthase that produces pentaketide chromone.

Journal: Acta crystallographica. Section F, Structural biology and crystallization communications 20060901

Title: [Study on the constituents from Neonauclea sessilifolia].

Journal: Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials 20021201

Title: Anti-AIDS agents, 10. Acacetin-7-O-beta-D-galactopyranoside, an anti-HIV principle from Chrysanthemum morifolium and a structure-activity correlation with some related flavonoids.

Journal: Journal of natural products 19940101

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