Emami S - Search Results

1

Synthesis, in vitro cytotoxicity and apoptosis inducing study of 2-aryl-3-nitro-2H-chromene derivatives as potent anti-breast cancer agents.

Rahmani-Nezhad S, Safavi M, Pordeli M, Ardestani SK, Khosravani L, Pourshojaei Y, Mahdavi M, Emami S, Foroumadi A, Shafiee A. Rahmani-Nezhad S, et al. Among authors: emami s. Eur J Med Chem. 2014 Oct 30;86:562-9. doi: 10.1016/j.ejmech.2014.09.017. Epub 2014 Sep 6. Eur J Med Chem. 2014. PMID: 25216378

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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