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CN1[C@@H]2C[C@@H](O)C[C@H]1[C@@H]1O[C@H]21
Solubility: DMSO: 56 mg/mL(201
binds convincingly within the ATP-binding site of Pim-1 suggesting an ATP-competitive inhibitory mechanism
is efficacious therapy for microbiologically proven chancroid in patients who do not have concurrent HIV-1 infection
Liproxstatin-1 (10 mg/kg
Telotristat 845 CN1[C@@H]2C[C@@H](O)C[C@H]1[C@@H]1O[C@H]21Telotristat, also known as LP 778902, is the acid form of Telotristat ethyl, and the active metabolite of LX1606 (Telotristat etiprate), which is an orally bioavailable, small molecule, tryptophan hydroxylase (TPH) inhibitor and serotonin synthesis inhibitor with potential antiserotonergic activity. Blocking peripheral serotonin synthesis by telotristat reduces severity of both chemical and infection induced intestinal inflammation. Product