Evaluation of Novel 7-(hetero)aryl-substituted Pyrazolo[1, 5-a]pyrimidines as Phosphodiesterase-4 Inhibitors

By  

Letters in Drug Design & Discovery, Vol. 7, Iss. 6, 2010-07 ,pp. : 402-408

Bentham Science Publishers

Access to resources Recommend Favorite

Syntheses, Urease Inhibition, and Antimicrobial Studies of Some Chiral 3-Substituted-4-amino-5-thioxo-1H,4H-1,2,4-triazoles

By  

Medicinal Chemistry, Vol. 4, Iss. 6, 2008-11 ,pp. : 539-543

Bentham Science Publishers

Access to resources Recommend Favorite

Synthesis and Antitubercular Evaluation on Novel 1-Ethyl-5-(hetero)aryl- 1,6-dihydropyrazine-2,3-dicarbonitriles and 3-Cyano-1-ethyl-5-(hetero) aryl-2(1H)-pyrazinones

By  

Anti-Infective Agents, Vol. 14, Iss. 2, 2016-09 ,pp. : 139-144

Bentham Science Publishers

Access to resources Recommend Favorite

Design, Synthesis and in silico Studies of New 5-substituted-2-(2-(5-aryl- 1H-1, 2, 4-triazole-3-ylthio) acetyl) Hydrazine Carbothioamide/ Carboxamides for Anticonvulsant Activity

By  

Letters in Drug Design & Discovery, Vol. 14, Iss. 10, 2017-09 ,pp. : 1155-1163

Bentham Science Publishers

Access to resources Recommend Favorite

6-Substituted 1H-quinolin-2-ones and 2-methoxy-quinolines: Synthesis and evaluation as inhibitors of steroid 5 reductases types 1 and 2

By Baston E.   Palusczak A.   Hartmann R.W.  

European Journal of Medicinal Chemistry, Vol. 35, Iss. 10, 2000-10 ,pp. : 931-940

Elsevier

Access to resources Recommend Favorite