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Restrict the search for
alpha-tocopherol acetate
to a specific field?
Class (Stereo):
CHEMICAL (ACHIRAL)
Etarotene (Ro 15-1570) is an arotinoid sulfone. Etarotene inhibits RNase P, a ribonucleoprotein that endonucleolytically cleaves all tRNA precursors to produce the mature 5' end, thereby affecting tRNA biogenesis. Etarotene has antikeratinizing potential. It was undergoing phase III clinical trials with Roche in the US for the treatment of psoriasis and other skin.
Status:
Investigational
Source:
NCT02272478: Phase 2/Phase 3 Interventional Unknown status Acute Myeloid Leukaemia
(2014)
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Targets:
Ganetespib (formerly called STA-9090) is a novel, injectable resorcinolic triazolone small molecule inhibitor of Hsp90, developed by Synta Pharmaceuticals. Ganetespib inhibits the growth of many tumor types in vitro and in vivo including AML, ALL, CML, NHL, neuroblastoma, Ewing sarcoma, rhabdoid cancer, rhabdomyosarcoma, melanoma, and carcinomas of the breast, lung, prostate, bladder and colon7-10,14-27. Ganetespib has being studied in multiple adult oncology indications. The 50% inhibitory concentrations (IC50) for Ganetespib against malignant mast cell lines are 10-50 times lower than that for 17-AAG, indicating that triazolone class of HSP90 inhibitors likely exhibits greater potency than geldanamycin based inhibitors. Ganetespib inhibits MG63 cell lines with IC50 of 43 nM. Ganetespib binds to the ATP-binding domain at the N-terminus of Hsp90 and serves as a potent Hsp90 inhibitor by causing degradation of multiple oncogenic Hsp90 client proteins including HER2/neu, mutated EGFR, Akt, c-Kit, IGF-1R, PDGFRα, Jak1, Jak2, STAT3, STAT5, HIF-1α, CDC2 and c-Met as well as Wilms' tumor 1. Ganetespib, at low nanomolar concentrations, potently arrests cell proliferation and induces apoptosis in a wide variety of human cancer cell lines, including many receptor tyrosine kinase inhibitor- and tanespimycin-resistant cell lines. Ganetespib exhibits potent cytotoxicity in a range of solid and hematologic tumor cell lines, including those that express mutated kinases that confer resistance to small-molecule tyrosine kinase inhibitors. Ganetespib has been studied in 5 completed Synta-sponsored clinical trials (Studies 9090-02, 9090-03, 9090-04, 9090-05, and 9090-07) and 3 completed Synta-sponsored studies in normal healthy volunteers (9090-12, 9090-13, and 9090-15). Ganetespib is currently being studied in 6 Synta-sponsored clinical trials. Studies include: one Phase 1 study, three Phase 2 studies, one Phase 2b study, and one Phase 3 study. Ganetespib is also being studied in 24 Investigator Sponsored Trials (ISTs)
Status:
Investigational
Source:
INN:tocofenoxate [INN]
Source URL:
Class (Stereo):
CHEMICAL (MIXED)
Tocofenoxate is a semisynthetic tocopherol derivative. Vitamin E supplement.
Class (Stereo):
CHEMICAL (UNKNOWN)
Dioxethedrin is the ephedrine derivative. It is the beta-adrenergic agonist. As a bronchodilator and sympathomimetic agent is was used in antitussive syrup Bexol.
Class (Stereo):
CHEMICAL (UNKNOWN)
Menabitan is a synthetic cannabinoid exerting analgesic activity.
Class (Stereo):
CHEMICAL (RACEMIC)
Acridorex (BS 7573a) is an anorectic agent.
Class (Stereo):
CHEMICAL (ABSOLUTE)
Medorubicin is an antineoplastic agent.
Status:
Investigational
Source:
INN:mecloxamine [INN]
Source URL:
Class (Stereo):
CHEMICAL (MIXED)
Mecloxamine is an anticholinergic exerting sedative and hypnotic activity.
Status:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Algestone acetonide is a cyclic ketal that is the 16α,17α-acetonide derivative of algestone. It is a steroidal progestin used as a contraceptive drug and anti-inflammatory agent (topical).
Class (Stereo):
CHEMICAL (ABSOLUTE)
Targets:
Conditions:
Vinrosidine (leurosidine) is a leurosine-like alkaloid originally isolated from Vinca rosea Linn. Vinrosidine exerts antitumor activity in animal models.
