Cyclisation of 3-[cyclopent-2-enyl]-4-hydroxy[1]benzopyran-2-one [PDF]
1248-12523-[Cyclopent-2-enyl]-4-hydroxy[1]benzopyran-2-one 3 has been prepared by the reaction of 3-chlorocyclopent-2-ene 2 and 4-hydroxy[1]benzopyran-2-one 1. Compound 3 or its acetate 4 on treatment with pyridine hydrotribromide in dichloromethane
Biswas, P, Majumdar, K C, Choudhury, P K
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Synthesis and cytotoxity of novel benzopyran derivatives
1619-1629In-vitro cytotoxic activity of benzopyrones and benzopyran derivatives has been evaluated against a panel of several human cancer cell lines.
Tripathi, Anil K +6 more
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En este trabajo se presenta el estudio de síntesis, caracterización y aplicación catalítica de hidróxidos doble laminares y Iodo en la obtención de benzopiran-2-onas.
Miguel Vázquez Guevara +5 more
doaj
2-(3,4-Dimethoxyphenyl)-5,7-dimethoxy-3,8-dimethyl-4H-1-benzopyran-4-one
The crystal structure of 2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-3,8-dimethyl-4H-1-benzopyran-4-one (alternatively 3',4'-dimethoxyphenyl-5,7-dimethoxy-3,8-dimethylflavone),C21H22O6, known to be a potent and selective inhibitor of rat heart cytosolic cyclic
Stomberg, Rolf +2 more
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From biomass to bioactivity: <i>Butea monosperma</i> bark-derived carbon quantum dots for benzopyran synthesis and their <i>in silico</i> studies. [PDF]
Teli S +4 more
europepmc +1 more source
Development of a Second-Generation RARα Selective Antagonist as an Orally Bioavailable, Effective, Safe, and Reversible Male Contraceptive. [PDF]
Shi R +8 more
europepmc +1 more source
Synthesis of Benzopyrans and Quinolines with Nitrogenated Chain and Their Cytotoxicity Against Human Cancer Cell Lines. [PDF]
Álvaro BS +8 more
europepmc +1 more source
Nordihydroguaiaretic acid attenuates TNFα-dependent intercellular adhesion molecule-1 expression in cultured human umbilical vein endothelial cells via targeting TNFα-PI3K-NF-κB-ICAM1 pathway. [PDF]
Mukherjee TK +4 more
europepmc +1 more source
A series of optically active tetrahydro-oxazino[2,3-c] benzopyran derivatives have been synthesized and evaluated for potassium channel opening activity. (4aR,11bR)-1-Benzoyl -5,5-dimethyl-2,3,4a,11b-tetrahydro -oxazino[2,3-c]benzopyran -9-carbonitrile ((
TSAI, MING-CHENG, 蔡明正
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Rational Design and Evaluation of Novel TGR5 Agonists for Diabetes. [PDF]
Bhimanwar RS +9 more
europepmc +1 more source

