Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Atul Khandwala"'
Autor:
Mark Holodniy, Jamey M Schmidt, James E Pennington, Mark Mistal, Steven B. Porter, Atul Khandwala, Johannes Koch
Publikováno v:
American Journal of Gastroenterology. 94:3267-3273
The aim of this study was to investigate the safety and effectiveness of orally administered SP-303 in patients with AIDS and diarrhea.This is a multicenter, phase II, randomized, double blind, placebo-controlled study. HIV-positive subjects with a h
Publikováno v:
Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons. 51(3)
A double-blind trial of amlexanox (C16H14N2O4) was carried out in 32 patients with recurrent oral aphthous ulcerations. During the treatment period, which lasted for 3 days, patients received either placebo topical paste or 5% amlexanox paste. The pa
Publikováno v:
Biochemical Pharmacology. 36:673-682
REV 2871 (CHBZ) was taken up by rat mast cells and human leukocytes in a specific and saturable manner. The compound can be hydrolyzed by a granule-associated enzyme in the mast cell to an ionic metabolite (REV 3579) whose in vitro profile is identic
Publikováno v:
Drug Development Research. 3:213-219
In vitro models of anaphylaxis such as the release of mediators from the mast cell can do more than identify compounds with intrinsic anti-allergic activity; they have the potential for development of a detailed profile of activity that may be compar
Autor:
Howard Jones, Ira Weinryb, Theaddeus Pruss, Atul Khandwala, Stephen M. Coutts, Edward S. Neiss
Publikováno v:
Biochemical Pharmacology. 36:663-672
REV 2871 (CHBZ) and its putative metabolite REV 3579-Z (also designated in the literature as RHC 3579-Z) were shown to be potent and orally effective inhibitors of passive cutaneous anaphylaxis (PCA) in the rat (ED 50 = 12 mg/kg). The activity profil
Publikováno v:
Journal of Cardiovascular Pharmacology. 8:S29-S32
Celiprolol HC1 is a new cardioselective beta-blocker with properties which may make it the next advance in the evolution of this class of compounds. Its cardioselectivity has been demonstrated both in vitro and in vivo, with an intravenous potency eq
Autor:
John H. Musser, S. Sciortino, Mitchell J. Leibowitz, P. Sonnino-Goldman, Kevin Bailey, Atul Khandwala, Howard Jones, Stephen M. Coutts, Edward S. Neiss, P. S. Wolf
Publikováno v:
Journal of Medicinal Chemistry. 28:1255-1259
A series of new 1,3-oxazolo[4,5-h]quinolines has been prepared. These compounds were tested as inhibitors of antigen-induced release of histamine (AIR) in vitro from rat peritoneal mast cells (RMC) and as inhibitors of IgE-mediated passive cutaneous
Autor:
J. Bernard L. Gee, Atul Khandwala
Publikováno v:
Biochemical Pharmacology. 23:1781-1786
Autor:
Atul Khandwala, J. Bernard L. Gee
Publikováno v:
Chest. 67:60S-63S
Autor:
Shoupe T Scott, Atul Khandwala, Ira Weinryb, Lewis J. Klunk, Stephen M. Coutts, John H. Musser
Publikováno v:
Agents and Actions. 18:318-324
CHBZ is a novel, non-disodium cromoglycate (DSCG)-like, antiallergic drug in vitro. Whereas DSCG loses antisecretory activity with increasing time of preincubation with rat mast cells (RMC) before antigen challenge, and does not inhibit non-immunolog