Emami S - Search Results

1

Synthesis and anti-Helicobacter pylori activity of 5-(nitroaryl)-1,3,4-thiadiazoles with certain sulfur containing alkyl side chain.

Foroumadi A, Rineh A, Emami S, Siavoshi F, Massarrat S, Safari F, Rajabalian S, Falahati M, Lotfali E, Shafiee A. Foroumadi A, et al. Among authors: emami s. Bioorg Med Chem Lett. 2008 Jun 1;18(11):3315-20. doi: 10.1016/j.bmcl.2008.04.033. Epub 2008 Apr 15. Bioorg Med Chem Lett. 2008. PMID: 18442909

2

Synthesis and antibacterial activity of some novel N-substituted piperazinyl-quinolones.

Foroumadi A, Davood A, Mirzaei M, Emami S, Moshafi MH. Foroumadi A, et al. Among authors: emami s. Boll Chim Farm. 2001 Nov-Dec;140(6):411-6. Boll Chim Farm. 2001. PMID: 11822230

3

Antituberculosis agents. III. In vitro evaluation of antimycobacterial activity and cytotoxicity of some N-piperazinyl quinolone derivatives.

Foroumadi A, Soltani F, Emami S, Davood A. Foroumadi A, et al. Among authors: emami s. Boll Chim Farm. 2002 May-Jun;141(3):247-9. Boll Chim Farm. 2002. PMID: 12197426

4

Stereoselective synthesis and in vitro antifungal evaluation of (E)- and (Z)-imidazolylchromanone oxime ethers.

Emami S, Falahati M, Banifatemi A, Moshiri K, Shafiee A. Emami S, et al. Arch Pharm (Weinheim). 2002 Jul;335(7):318-24. doi: 10.1002/1521-4184(200209)335:7<318::AID-ARDP318>3.0.CO;2-O. Arch Pharm (Weinheim). 2002. PMID: 12207281

5

Antituberculosis agents. V. Synthesis, evaluation of in vitro antituberculosis activity and cytotoxicity of some 2-(5-nitro-2-furyl)-1,3,4-thiadiazole derivatives.

Foroumadi A, Asadipour A, Mirzaei M, Karimi J, Emami S. Foroumadi A, et al. Among authors: emami s. Farmaco. 2002 Sep;57(9):765-9. doi: 10.1016/s0014-827x(02)01277-6. Farmaco. 2002. PMID: 12385528

6

Synthesis and in vitro antibacterial activity of N-[5-(5-nitro-2-furyl)-1,3,4-thiadiazole-2-yl] piperazinyl quinolone derivatives.

Foroumadi A, Ashraf-Askari R, Moshafi MH, Emami S, Zeynali A. Foroumadi A, et al. Among authors: emami s. Pharmazie. 2003 Jun;58(6):432-3. Pharmazie. 2003. PMID: 12857013 No abstract available.

7

(E)- and (Z)-1,2,4-triazolylchromanone oxime ethers as conformationally constrained antifungals.

Emami S, Falahati M, Banifatemi A, Amanlou M, Shafiee A. Emami S, et al. Bioorg Med Chem. 2004 Aug 1;12(15):3971-6. doi: 10.1016/j.bmc.2004.06.010. Bioorg Med Chem. 2004. PMID: 15246073

8

Stereoselective synthesis and antifungal activity of (Z)-trans-3-azolyl-2-methylchromanone oxime ethers.

Emami S, Falahati M, Banifatemi A, Shafiee A. Emami S, et al. Bioorg Med Chem. 2004 Nov 15;12(22):5881-9. doi: 10.1016/j.bmc.2004.08.030. Bioorg Med Chem. 2004. PMID: 15498664

9

Synthesis and in vitro leishmanicidal activity of 2-(1-methyl-5-nitro-1H-imidazol-2-yl)-5-substituted-1,3,4-thiadiazole derivatives.

Foroumadi A, Emami S, Pournourmohammadi S, Kharazmi A, Shafiee A. Foroumadi A, et al. Among authors: emami s. Eur J Med Chem. 2005 Dec;40(12):1346-50. doi: 10.1016/j.ejmech.2005.07.002. Epub 2005 Aug 10. Eur J Med Chem. 2005. PMID: 16095763

10

Synthesis and antibacterial activity of N-(5-benzylthio-1,3,4-thiadiazol-2-yl) and N-(5-benzylsulfonyl-1,3,4-thiadiazol-2-yl)piperazinyl quinolone derivatives.

Foroumadi A, Emami S, Hassanzadeh A, Rajaee M, Sokhanvar K, Moshafi MH, Shafiee A. Foroumadi A, et al. Among authors: emami s. Bioorg Med Chem Lett. 2005 Oct 15;15(20):4488-92. doi: 10.1016/j.bmcl.2005.07.016. Bioorg Med Chem Lett. 2005. PMID: 16105736

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