S. Ahmad

发表

Design and synthesis of 4-substituted benzamides as potent, selective, and orally bioavailable I(Ks) blockers.

A. Mathur, P. Stein, M. Conder, 2001, Journal of Medicinal Chemistry.

Arylcyclopropanecarboxyl guanidines as novel, potent, and selective inhibitors of the sodium hydrogen exchanger isoform-1.

K. J. Yost, M. Kirby, N. Grazier, 2001, Journal of medicinal chemistry.

A convenient method for the synthesis of 3.beta.-hydroxy 4-en-6-one steroids

Shafiullah, Shamsuzzaman, S. Ahmad, 1991 .

Inhibition of pig kidney L-aromatic amino acid decarboxylase by 2,3-methano-m-tyrosines.

R. Phillips, C. Stammer, S. Ahmad, 1992, Journal of medicinal chemistry.

Synthesis of the 11-membered cytochalasin ring system by modified reformatsky cyclization

E. Vedejs, S. Ahmad, 1988 .

Inhibition of steel corrosion by some new triazole derivatives in boiling hydrochloric acid

M. Quraishi, S. Ahmad, M. Ansari, 1997 .

Facile synthesis of 1-alkoxy-1H-benzo- and 7-azabenzotriazoles from peptide coupling agents, mechanistic studies, and synthetic applications

M. Singh, Mukesh Kumar, Raghu Ram Chamala, 2014, Beilstein journal of organic chemistry.

A facile method for synthesis of N-acyloxymethyl-5-fluorouracils, as a class of antitumor agents.

M. Iigo, A. Hoshi, S. Ozaki, 1987, Chemical & pharmaceutical bulletin.

New guanine deaminase inhibitors.

A. Saxena, K. Shanker, S. Ahmad, 1984, Pharmacological research communications.

Anticonvulsant & MAO inhibitory activity of substituted quinazolones.

K. Bhargava, K. K. Tangri, J. Barthwal, 1981, Indian journal of experimental biology.