V M Girijavallabhan - JoVE Visualize

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Current Medicinal Chemistry|September 20, 2001

Farnesyl protein transferase inhibition: a novel approach to anti-tumor therapy. the discovery and development of SCH 66336A K Ganguly, R J Doll, V M Girijavallabhan

The Journal of Antimicrobial Chemotherapy|June 1, 1985

Synthesis and preliminary in-vitro profile of Sch 34343--a new penem antibacterial agentA K Ganguly, A Afonso, V M Girijavallabhan, et al.

The Journal of Antibiotics|May 1, 1982

Chemical modification of everninomicinsA K Ganguly, V M Girijavallabhan, G H Miller, et al.

Bioorganic & Medicinal Chemistry Letters|January 1, 1999

Novel HIV-protease inhibitors containing beta-hydroxyether and -thioether dipeptide isostere surrogates: modification of the P3 ligandN M Patel, F Bennett, V M Girijavallabhan, et al.

Bioorganic & Medicinal Chemistry|October 1, 1994

The synthesis of novel HIV-protease inhibitorsV M Girijavallabhan, F Bennett, N M Patel, et al.

The Journal of Organic Chemistry|September 2, 2000

Enzymatic kinetic resolution of piperidine atropisomers: synthesis of a key intermediate of the farnesyl protein transferase inhibitor, SCH66336B Morgan, A Zaks, D R Dodds, et al.

Journal of Medicinal Chemistry|October 30, 1992

Isobenzofurans as conformationally constrained miconazole analogues with improved antifungal potencyR G Lovey, A J Elliott, J J Kaminski, et al.

Bioorganic & Medicinal Chemistry|July 10, 1999

Atropisomeric trihalobenzocycloheptapyridine analogues provide stereoselective FPT inhibitors with antitumor activityF G Njoroge, B Vibulbhan, W R Bishop, et al.

Cancer Chemotherapy and Pharmacology|January 29, 1999

Effects of SCH 59228, an orally bioavailable farnesyl protein transferase inhibitor, on the growth of oncogene-transformed fibroblasts and a human colon carcinoma xenograft in nude miceM Liu, M S Bryant, J Chen, et al.

Journal of Medicinal Chemistry|June 23, 1999

Tricyclic farnesyl protein transferase inhibitors: crystallographic and calorimetric studies of structure-activity relationshipsC L Strickland, P C Weber, W T Windsor, et al.

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Showing results (1-10 of 14) with videos related to

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Pageof 2

Current Medicinal Chemistry|September 20, 2001

Farnesyl protein transferase inhibition: a novel approach to anti-tumor therapy. the discovery and development of SCH 66336A K Ganguly, R J Doll, V M Girijavallabhan

The Journal of Antimicrobial Chemotherapy|June 1, 1985

Synthesis and preliminary in-vitro profile of Sch 34343--a new penem antibacterial agentA K Ganguly, A Afonso, V M Girijavallabhan, et al.

The Journal of Antibiotics|May 1, 1982

Chemical modification of everninomicinsA K Ganguly, V M Girijavallabhan, G H Miller, et al.

Bioorganic & Medicinal Chemistry Letters|January 1, 1999

Novel HIV-protease inhibitors containing beta-hydroxyether and -thioether dipeptide isostere surrogates: modification of the P3 ligandN M Patel, F Bennett, V M Girijavallabhan, et al.

Bioorganic & Medicinal Chemistry|October 1, 1994

The synthesis of novel HIV-protease inhibitorsV M Girijavallabhan, F Bennett, N M Patel, et al.

The Journal of Organic Chemistry|September 2, 2000

Enzymatic kinetic resolution of piperidine atropisomers: synthesis of a key intermediate of the farnesyl protein transferase inhibitor, SCH66336B Morgan, A Zaks, D R Dodds, et al.

Journal of Medicinal Chemistry|October 30, 1992

Isobenzofurans as conformationally constrained miconazole analogues with improved antifungal potencyR G Lovey, A J Elliott, J J Kaminski, et al.

Bioorganic & Medicinal Chemistry|July 10, 1999

Atropisomeric trihalobenzocycloheptapyridine analogues provide stereoselective FPT inhibitors with antitumor activityF G Njoroge, B Vibulbhan, W R Bishop, et al.

Cancer Chemotherapy and Pharmacology|January 29, 1999

Effects of SCH 59228, an orally bioavailable farnesyl protein transferase inhibitor, on the growth of oncogene-transformed fibroblasts and a human colon carcinoma xenograft in nude miceM Liu, M S Bryant, J Chen, et al.

Journal of Medicinal Chemistry|June 23, 1999

Tricyclic farnesyl protein transferase inhibitors: crystallographic and calorimetric studies of structure-activity relationshipsC L Strickland, P C Weber, W T Windsor, et al.

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