95903-37-0Relevant academic research and scientific papers
Targeting Tumor Associated Carbonic Anhydrases IX and XII: Highly Isozyme Selective Coumarin and Psoralen Inhibitors
Melis, Claudia,Distinto, Simona,Bianco, Giulia,Meleddu, Rita,Cottiglia, Filippo,Fois, Benedetta,Taverna, Domenico,Angius, Rossella,Alcaro, Stefano,Ortuso, Francesco,Gaspari, Marco,Angeli, Andrea,Del Prete, Sonia,Capasso, Clemente,Supuran, Claudiu T.,Maccioni, Elias
supporting information, p. 725 - 729 (2018/06/18)
A small library of psoralen carboxylic acids and their corresponding benzenesulfonamide derivatives were designed and synthesized to evaluate their activity and selectivity toward tumor associated human carbonic anhydrase (hCA) isoforms IX and XII. Both p
Novel photochromic 3-(3-coumarinyl)-4-(3-thienyl)maleic acid cyclic derivatives
Traven, Valery F.,Bochkov, Andrei Yu.,Krayushkin, Mikhail M.,Yarovenko, Vladimir N.,Barachevsky, Valery A.,Beletskaya, Irina P.
experimental part, p. 22 - 24 (2010/04/23)
Novel unsymmetrical photosensitive derivatives of maleic acid, anhydride and N-alkylimide, including coumarin and thiophene moieties, have been designed and synthesized; their photochromism study and fatigue resistance estimation are reported.
Modified coumarins. 10. Synthesis of substituted 2-(7-oxofuro[3,2-g] chromen-6-yl) acetic acids
Nagorichna,Dubovik,Garazd,Khilya
, p. 253 - 261 (2007/10/03)
Substituted 2-(7-oxofuro[3,2-g]chromen-6-yl) acetic acids, modified psoralen analogs, were synthesized by linear fusion of a furan ring to the coumarin system.
4-oxo-benzopyran carboxylic acids
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, (2008/06/13)
Compounds of the Formula I: STR1 and pharmaceutically acceptable salts thereof are leukotriene antagonists. These compounds inhibit SRS-A and leukotriene synthesis and are antagonists of SRS-A and are thus useful in the treatment of asthma, allergic disorders, inflammation, skin diseases and certain cardiovascular disorders.
