Weight | 489.406 g/mol |
---|---|
Formula | C27H22Cl2N4O |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 1 |
Aromatic Rings | 5 |
Rotatable Bonds | 4 |
Tipifarnib (192185-68-5, 192185-72-1)
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- Sigma-Aldrich - Tipifarnib99.00 - 399.00 USD
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- Phase III Trial of Gemcitabine Plus Tipifarnib Compared With Gemcitabine Plus Placebo in Advanced Pancreatic Cancer (Journal of Clinical Oncology, 2004)
- Farnesyltransferase inhibitor tipifarnib is well tolerated, induces stabilization of disease, and inhibits farnesylation and oncogenic/tumor survival pathways in patients with advanced multiple myeloma (Blood, 2004)
- A phase 2 study of the farnesyltransferase inhibitor tipifarnib in poor-risk and elderly patients with previously untreated acute myelogenous leukemia (Blood, 2007)
- Phase II trial of tipifarnib in patients with recurrent malignant glioma either receiving or not receiving enzyme-inducing antiepileptic drugs : a North American Brain Tumor Consortium Study (Journal of Clinical Oncology, 2006)
- Phase I Trial and Pharmacokinetic Study of the Farnesyltransferase Inhibitor Tipifarnib in Children With Refractory Solid Tumors or Neurofibromatosis Type I and Plexiform Neurofibromas (Journal of Clinical Oncology, 2006)
- A randomized phase 3 study of tipifarnib compared with best supportive care, including hydroxyurea, in the treatment of newly diagnosed acute myeloid leukemia in patients 70 years or older (Blood, 2009)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1C=NC=C1C(C2=CC=C(C=C2)Cl)(C3=CC4=C(C=C3)N(C(=O)C=C4C5=CC(=CC=C5)Cl)C)N
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InChIKeyPLHJCIYEEKOWNM-UHFFFAOYSA-N
- Pubchem - Tipifarnib
- Wikipedia - Tipifarnib
Tipifarnib (INN, proposed trade name Zarnestra) is a farnesyltransferase inhibitor that is being investigated in patients 65 years of age and older with newly diagnosed acute myeloid leukemia (AML). It inhibits the Ras kinase in a post-translational modification step before the kinase pathway becomes hyperactive. It inhibits prenylation of the CaaX tail motif, which allows Ras to bind to the membrane where it is active.
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