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10140-70-2

10140-70-2 | 2H-3-Benzoxacyclododecin-2,10(1H)-dione, 4,5,6,7,8,9-hexahydro-11,13-dihydroxy-4-methyl-, (4S)-

CAS No: 10140-70-2 Catalog No: AG0004ER MDL No:

Product Description

Catalog Number:
AG0004ER
Chemical Name:
2H-3-Benzoxacyclododecin-2,10(1H)-dione, 4,5,6,7,8,9-hexahydro-11,13-dihydroxy-4-methyl-, (4S)-
CAS Number:
10140-70-2
Molecular Formula:
C16H20O5
Molecular Weight:
292.3270
IUPAC Name:
(5S)-13,15-dihydroxy-5-methyl-4-oxabicyclo[10.4.0]hexadeca-1(12),13,15-triene-3,11-dione
InChI:
InChI=1S/C16H20O5/c1-10-5-3-2-4-6-13(18)16-11(8-15(20)21-10)7-12(17)9-14(16)19/h7,9-10,17,19H,2-6,8H2,1H3/t10-/m0/s1
InChI Key:
VDUIGYAPSXCJFC-JTQLQIEISA-N
SMILES:
C[C@H]1CCCCCC(=O)c2c(CC(=O)O1)cc(O)cc2O
UNII:
WT39K5T3BX

Properties

Complexity:
381  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
292.131g/mol
Formal Charge:
0
Heavy Atom Count:
21  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
292.331g/mol
Monoisotopic Mass:
292.131g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
83.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.1  

Literature

Title Journal
[Biological activity of Penicillium sp. 10-51 exometabolites]. Mikrobiolohichnyi zhurnal (Kiev, Ukraine : 1993) 20120101
Aryne acyl-alkylation in the general and convergent synthesis of benzannulated macrolactone natural products: an enantioselective synthesis of (-)-curvularin. Organic letters 20100402
Transcriptional and post-transcriptional regulation of iNOS expression in human chondrocytes. Biochemical pharmacology 20100301
Isolation and difference in anti-Staphylococcus aureus bioactivity of curvularin derivates from fungus Eupenicillium sp. Applied biochemistry and biotechnology 20091001
Metabolite production by different Ulocladium species. International journal of food microbiology 20080815
Inhibitors of inducible NO synthase expression: total synthesis of (S)-curvularin and its ring homologues. ChemMedChem 20080601
First total syntheses and spectral data corrections of 11-alpha-methoxycurvularin and 11-beta-methoxycurvularin. The Journal of organic chemistry 20071207
A concise synthetic approach to beta,gamma-dehydrocurvularin: synthesis of (+/-)-di-O-methyl-beta,gamma-dehydrocurvularin. Bioscience, biotechnology, and biochemistry 20070601
Microbial transformation of curvularin. Journal of natural products 20050801
A new anthraquinone and cytotoxic curvularins of a Penicillium sp. from the rhizosphere of Fallugia paradoxa of the Sonoran desert. The Journal of antibiotics 20040501
Betagamma-dehydrocurvularin and related compounds as nematicides of Pratylenchus penetrans from the fungus Aspergillus sp. Bioscience, biotechnology, and biochemistry 20030601
Total synthesis of (s)-(+)-citreofuran by ring closing alkyne metathesis. The Journal of organic chemistry 20030221
Sporogen, S14-95, and S-curvularin, three inhibitors of human inducible nitric-oxide synthase expression isolated from fungi. Molecular pharmacology 20030201
Online analysis of xestodecalactones A-C, novel bioactive metabolites from the fungus Penicillium cf. montanense and their subsequent isolation from the sponge Xestospongia exigua. Journal of natural products 20021101

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