- Bafetinib USP/EP/BP
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- $1.10 / 1g
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2021-07-07
- CAS:859212-16-1
- Min. Order: 1g
- Purity: 99.9%
- Supply Ability: 100 Tons Min
- Bafetinib
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- $1.00 / 1kg
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2019-07-06
- CAS:859212-16-1
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 100KG
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| Bafetinib Basic information |
Product Name: | Bafetinib | Synonyms: | Benzamide, N-(3-((4,5'-bipyrimidin)-2-ylamino)-4-methylphenyl)-4-(((3S)-3-(dimethylamino)-1-pyrrolidinyl)methyl)-3-(trifluoromethyl)-;Inno 406;Inno-406;4-[[(3S)-3-Dimethylaminopyrrolidin-1-yl]methyl]-N-[4-methyl-3-[(4-pyrimidin-5-ylpyrimidin-2-yl)amino]phenyl]-3-(trifluoromethyl)benzamide;Ns 187;Unii-nvw4Z03I9b;Bafetinib (INNO-406);N-[3-([4,5'-BipyriMidin]-2-ylaMino)-4-Methylphenyl]-4-[[(3S)-3-(diMethylaMino)-1-pyrrolidinyl]Methyl]-3-(trifluoroMethyl)benzaMide | CAS: | 859212-16-1 | MF: | C30H31F3N8O | MW: | 576.62 | EINECS: | | Product Categories: | Aromatics;Chiral Reagents;Heterocycles;Inhibitors;Intermediates & Fine Chemicals;Pharmaceuticals | Mol File: | 859212-16-1.mol | |
| Bafetinib Chemical Properties |
Melting point | 166-168°C | density | 1.36±0.1 g/cm3(Predicted) | storage temp. | Refrigerator | solubility | DMSO:42.0(Max Conc. mg/mL);72.84(Max Conc. mM) | form | A crystalline solid | pka | 12.72±0.70(Predicted) |
| Bafetinib Usage And Synthesis |
Description | Bcr-Abl, a fusion protein with deregulated tyrosine kinase activity, is highly expressed in chronic myelogenous leukemia (CML). Bafetinib is a rationally developed tyrosine kinase inhibitor based on the chemical structure of imatinib , with modifications added to improve binding and potency against Bcr-Abl kinase (IC50 = 5.8 nM). It is 25- to 55-fold more potent than imatinib in vitro and ≥10-fold more potent in vivo. Bafetinib inhibits 12 out of the 13 most frequent imatinib-resistant Bcr-Abl point mutations, but not the T315I mutation and also targets the Src family kinase Lyn (IC50 = 19 nM), which has been associated with resistance to imatinib in CML. | Chemical Properties | Pale Yellow Solid | Uses | A substituted benzamide derivative structurally related to STI-571 (Imatinib Mesylate). It was identified as highly potent Bcr-Abl kinase inhibitor. |
| Bafetinib Preparation Products And Raw materials |
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