Chemical Structure : RITA
CAS No.: 213261-59-7
Catalog No.: PC-22936Not For Human Use, Lab Use Only.
RITA is a small molecule inhibitor of the protein-protein interaction between p53 and human double minute-2 (HDM-2), binds to p53 with an apparent Kd value of 1.5 nM and prevents the interaction between p53 and HDM-2.
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10 mg | $98 | In stock | |
25 mg | $168 | In stock | |
50 mg | $268 | In stock | |
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RITA is a small molecule inhibitor of the protein-protein interaction between p53 and human double minute-2 (HDM-2), binds to p53 with an apparent Kd value of 1.5 nM and prevents the interaction between p53 and HDM-2.
RITA induces DNA damage and apoptosis in, as well as inhibits the growth of, A498, TK-10, ACHN, and UO-31 renal carcinoma cells (GI50s = 0.017, 0.032, 22.76, and 41.71 µM, respectively).
RITA (10 mg/kg) reduces tumor volume in an HCT116 mouse xenograft model.
RITA (45 mg/kg) induces complete tumor regression in an A498 mouse xenograft model when administered at a dose of 45 mg/kg.
M.Wt | 292.37 | |
Formula | C14H12O3S2 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
(5,5'-(Furan-2,5-diyl)bis(thiophene-5,2-diyl))dimethanol |
1. Chène, P, et al. Nat. Rev. Cancer 3, 102-109 (2003).
2. Issaeva, N., et al. Nat. Med. 10(12), 1321-1328 (2004).
3. Rivera, M.I., et al. Biochem. Pharmacol. 57(11), 1283-1295 (1999).
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