Company Name: |
TargetMol Chemicals Inc.
|
Tel: |
15002134094 |
Email: |
marketing@targetmol.cn |
Products Intro: |
Product Name:BIM-46050 CAS:201487-52-7 Purity:详情请点击官网 Package:1 mg
|
|
| BIM-46050 Basic information |
Product Name: | BIM-46050 | Synonyms: | BIM-46050;L-Methionine, N-[[(4R)-3-[(2S,3S)-2-[[(2R)-2-amino-3-mercaptopropyl]amino]-3-methylpentyl]-5,5-dimethyl-4-thiazolidinyl]carbonyl]- | CAS: | 201487-52-7 | MF: | C20H40N4O3S3 | MW: | 480.75 | EINECS: | | Product Categories: | | Mol File: | 201487-52-7.mol | |
| BIM-46050 Chemical Properties |
Boiling point | 699.7±55.0 °C(Predicted) | density | 1.162±0.06 g/cm3(Predicted) | pka | 3.32±0.10(Predicted) |
| BIM-46050 Usage And Synthesis |
Description | BIM-46050 is a potent and specific inhibitor of human farnesyltransferase. BIM-46050 is free acidic form of BIM-46068. The IC50 values for in vitro inhibition of human brain FTase indicate that BIM-46050 and the ester form BIM-46068 are potent inhibitors of farnesyltransferase. Their potencies are in the nanomolar range and compare favorably with the compounds B581, FTI-277 and L745,631. B581 is an analog of the tetrapeptide Cys-Val-Phe-Met obtained by replacement of the amino-terminal amide bonds inhibiting processing of farnesylated proteins specifically. FTI-277 is a methyl ester of FTI-276, reported as a preferential inhibitor of FTase over GGTase I (100-fold). L745,631 is a 2-substituted piperazine reported to be a highly selective inhibitor of FTase over GGTase (2,000-fold). The selectivity of BIM-46050 and BIM-46068 for FTase over GGTase is very similar for both compounds (3,000-fold). |
| BIM-46050 Preparation Products And Raw materials |
|