Patel M - Search Results

1

Synthesis and evaluation of analogs of Efavirenz (SUSTIVA) as HIV-1 reverse transcriptase inhibitors.

Patel M, Ko SS, McHugh RJ Jr, Markwalder JA, Srivastava AS, Cordova BC, Klabe RM, Erickson-Viitanen S, Trainor GL, Seitz SP. Patel M, et al. Bioorg Med Chem Lett. 1999 Oct 4;9(19):2805-10. doi: 10.1016/s0960-894x(99)00486-2. Bioorg Med Chem Lett. 1999. PMID: 10522695

2

Synthesis, antiviral activity and pharmacokinetics of P1/P1' substituted 3-aminoindazole cyclic urea HIV protease inhibitors.

Kaltenbach RF 3rd, Patel M, Waltermire RE, Harris GD, Stone BR, Klabe RM, Garber S, Bacheler LT, Cordova BC, Logue K, Wright MR, Erickson-Viitanen S, Trainor GL. Kaltenbach RF 3rd, et al. Among authors: patel m. Bioorg Med Chem Lett. 2003 Feb 24;13(4):605-8. doi: 10.1016/s0960-894x(02)01064-8. Bioorg Med Chem Lett. 2003. PMID: 12639540

3

Preparation and structure-activity relationship of novel P1/P1'-substituted cyclic urea-based human immunodeficiency virus type-1 protease inhibitors.

Nugiel DA, Jacobs K, Kaltenbach RF, Worley T, Patel M, Meyer DT, Jadhav PK, De Lucca GV, Smyser TE, Klabe RM, Bacheler LT, Rayner MM, Seitz SP. Nugiel DA, et al. Among authors: patel m. J Med Chem. 1996 May 24;39(11):2156-69. doi: 10.1021/jm960083n. J Med Chem. 1996. PMID: 8667359

4

The synthesis and evaluation of cyclic ureas as HIV protease inhibitors: modifications of the P1/P1' residues.

Patel M, Bacheler LT, Rayner MM, Cordova BC, Klabe RM, Erickson-Viitanen S, Seitz SP. Patel M, et al. Bioorg Med Chem Lett. 1998 Apr 7;8(7):823-8. doi: 10.1016/s0960-894x(98)00119-x. Bioorg Med Chem Lett. 1998. PMID: 9871548

5

The synthesis of symmetrical and unsymmetrical P1/P1' cyclic ureas as HIV protease inhibitors.

Patel M, Kaltenbach RF 3rd, Nugiel DA, McHugh RJ Jr, Jadhav PK, Bacheler LT, Cordova BC, Klabe RM, Erickson-Viitanen S, Garber S, Reid C, Seitz SP. Patel M, et al. Bioorg Med Chem Lett. 1998 May 5;8(9):1077-82. doi: 10.1016/s0960-894x(98)00175-9. Bioorg Med Chem Lett. 1998. PMID: 9871711

6

Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: novel biaryl indazoles as P2/P2' substituents.

Patel M, Rodgers JD, McHugh RJ Jr, Johnson BL, Cordova BC, Klabe RM, Bacheler LT, Erickson-Viitanen S, Ko SS. Patel M, et al. Bioorg Med Chem Lett. 1999 Nov 15;9(22):3217-20. doi: 10.1016/s0960-894x(99)00564-8. Bioorg Med Chem Lett. 1999. PMID: 10576691

7

Synthesis and evaluation of benzoxazinones as HIV-1 reverse transcriptase inhibitors. Analogs of Efavirenz (SUSTIVA).

Patel M, McHugh RJ Jr, Cordova BC, Klabe RM, Erickson-Viitanen S, Trainor GL, Ko SS. Patel M, et al. Bioorg Med Chem Lett. 1999 Nov 15;9(22):3221-4. doi: 10.1016/s0960-894x(99)00565-x. Bioorg Med Chem Lett. 1999. PMID: 10576692

8

Synthesis and evaluation of quinoxalinones as HIV-1 reverse transcriptase inhibitors.

Patel M, McHugh RJ Jr, Cordova BC, Klabe RM, Erickson-Viitanen S, Trainor GL, Rodgers JD. Patel M, et al. Bioorg Med Chem Lett. 2000 Aug 7;10(15):1729-31. doi: 10.1016/s0960-894x(00)00321-8. Bioorg Med Chem Lett. 2000. PMID: 10937734

9

Synthesis and evaluation of novel quinolinones as HIV-1 reverse transcriptase inhibitors.

Patel M, McHugh RJ Jr, Cordova BC, Klabe RM, Bacheler LT, Erickson-Viitanen S, Rodgers JD. Patel M, et al. Bioorg Med Chem Lett. 2001 Jul 23;11(14):1943-5. doi: 10.1016/s0960-894x(01)00331-6. Bioorg Med Chem Lett. 2001. PMID: 11459666

10

Hydrophobicity, a physicochemical factor in the inhibition of the enzyme estrone sulfatase (ES).

Ahmed S, James K, Owen CP, Patel CK, Patel M. Ahmed S, et al. Among authors: patel m, patel ck. Bioorg Med Chem Lett. 2001 Sep 17;11(18):2525-8. doi: 10.1016/s0960-894x(01)00482-6. Bioorg Med Chem Lett. 2001. PMID: 11549461

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