CAS NO: | 1430844-80-6 |
规格: | ≥98% |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
250mg | 电议 |
500mg | 电议 |
Molecular Weight (MW) | 658.81 |
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Formula | C38H38N6O3S |
CAS No. | 1430844-80-6 |
Storage | -20℃ for 3 years in powder form |
-80℃ for 2 years in solvent | |
Solubility(In vitro) | DMSO: 100 mg/mL (151.8 mM) |
Water: <1 mg/mL | |
Ethanol: <1 mg/mL | |
Solubility(In vivo) | NA |
Synonyms | A-1331852; A 1331852; A1331852 |
In Vitro | In vitroactivity: A-1331852 exhibits remarkable potency both as a single agent and in combination with TKIs in killing primary CD34+ CML cell. Also, It has remarkable potency in inducing apoptosis in these cells at low nanomolar concentrations as early as 1 h post-treatment Cell Assay: Immunoprecipitation of BCL-XL is carried out in K562 cells, exposed to A-1331852 (100 nM) for 0-2 h, and the eluted complexes are immunoblotted for the indicated proteins. The input cell lysates and the immunodepleted supernatant (labeled as Flow-through) are immunoblotted to check the efficiency of the immunoprecipitation. |
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In Vivo | Previous animal study found that A-1331852 could demonstrate antitumor efficacy in the Molt-4 xenograft model, such as tumor regressions as a single agent. In addition, in the NCI-H1963.FP5 xenograft model of SCLC, it was found that A-1331852 combined with venetoclax was able to recapitulate the efficacy of navitoclax |
Animal model | SCID and SCID-bg mice |
Formulation & Dosage | Formulated in 60% Phosal 50 PG, 27.5 % PEG 400, 10% ethanol, and 2.5% DMSO; 25 mg/kg; Oral gavage |
References | Sci Transl Med. 2015 Mar 18;7(279):279ra40; Leukemia. 2016 Jun;30(6):1273-81. |