Antitumor Activity of SCH 66336, an Orally Bioavailable Tricyclic Inhibitor of Farnesyl Protein Transferase, in Human Tumor Xenograft Models and Wap-ras Transgenic Mice (original) (raw)

Characterization of the antitumor effects of the selective farnesyl protein transferase inhibitor R115777 in vivo and in vitro

Alison Todd

Cancer research, 2001

View PDFchevron_right

Inhibitors of farnesyl:protein transferase—A possible cancer chemotherapeutic

Daniele Leonard

1996

View PDFchevron_right

Farnesyl Transferase Inhibitors as Potential Anticancer Agents

Sounak Bagchi

Mini Reviews in Medicinal Chemistry, 2018

View PDFchevron_right

Tricyclic Farnesyl Protein Transferase Inhibitors: Crystallographic and Calorimetric Studies of Structure−Activity Relationships †

Hung Le

Journal of Medicinal Chemistry, 1999

View PDFchevron_right

Structure−Activity Relationship of 3-Substituted N -(Pyridinylacetyl)-4- (8-chloro-5,6-dihydro-11 H -benzo[5,6]cyclohepta[1,2- b ]pyridin-11-ylidene)- piperidine Inhibitors of Farnesyl-Protein Transferase: Design and Synthesis of in Vivo Active Antitumor Compounds

Ming Liu, Amin Nomeir

Journal of Medicinal Chemistry, 1997

View PDFchevron_right

Preclinical antitumor activity and pharmacodynamic studies with the farnesyl protein transferase inhibitor R115777 in human breast cancer

Melanie Valenti

Clinical Cancer Research

View PDFchevron_right

Novel Tricyclic Inhibitors of Farnesyl Protein Transferase

George Njoroge

Journal of Biological Chemistry, 1995

View PDFchevron_right

NMR studies of novel inhibitors bound to farnesyl-protein transferase

Charles Omer

Protein Science, 2008

View PDFchevron_right

Conformation of a novel tetrapeptide inhibitor NH2-d-Trp-d-Met-Phe(pCl)-Gla-NH2 bound to farnesyl-protein transferase

A. Pessi

Journal of Peptide Research, 1999

View PDFchevron_right

Potent, Selective, and Orally Bioavailable Tricyclic Pyridyl Acetamide N -Oxide Inhibitors of Farnesyl Protein Transferase with Enhanced in Vivo Antitumor Activity

George Njoroge

Journal of Medicinal Chemistry, 1998

View PDFchevron_right

Farnesyl protein transferase inhibitors as targeted therapies for hematologic malignancies

Judith Karp

Seminars in Hematology, 2001

View PDFchevron_right

Potent and Selective Farnesyl Transferase Inhibitors

Juozas Domarkas

Journal of Medicinal Chemistry, 2004

View PDFchevron_right

Activity of SCH 66336, a tricyclic farnesyltransferase inhibitor, against human tumor colony-forming units

Elzbieta Izbicka

Annals of oncology : official journal of the European Society for Medical Oncology / ESMO, 1999

View PDFchevron_right

Non-thiol 3-aminomethylbenzamide inhibitors of farnesyl-protein transferase

Christopher Dinsmore

Bioorganic & Medicinal Chemistry Letters, 1999

View PDFchevron_right

Farnesyl Diphosphate-Based Inhibitors of Ras Farnesyl Protein Transferase

Veeraswamy Manne

Journal of Medicinal Chemistry, 1995

View PDFchevron_right

Preparation of a clinically investigated ras farnesyl transferase inhibitor

David Askin

Journal of Heterocyclic Chemistry, 2003

View PDFchevron_right

The synthesis and biological evaluation of a series of potent dual inhibitors of farnesyl and geranyl-Geranyl protein transferases

Michelle Ellis-Hutchings

Bioorganic & Medicinal Chemistry Letters, 2002

View PDFchevron_right

Evaluation of farnesyl:protein transferase and geranylgeranyl:protein transferase inhibitor combinations in preclinical models

Charles Omer

Cancer research, 2001

View PDFchevron_right

Streamlined Processes for the Synthesis of a Farnesyl Transferase Inhibitor Drug Candidate

Karl Ng

Organic Process Research & Development, 2004

View PDFchevron_right

Farnesyl transferase inhibitors: the next targeted therapies for breast cancer?

Fadlo Khuri

Endocrine Related Cancer, 2004

View PDFchevron_right

Synthesis and evaluation of a novel series of farnesyl protein transferase inhibitors as non-peptidic CAAX tetrapeptide analogues

Michel Cubas Perez

Bioorganic & Medicinal Chemistry Letters, 2003

View PDFchevron_right

The farnesyl protein transferase inhibitor SCH66336 is a potent inhibitor of MDR1 product P-glycoprotein

Christopher Casciano

Cancer research, 2001

View PDFchevron_right