Description
CNX-774 inhibits Bruton’s tyrosine kinase (BTK) and displays potential anticancer and immunosuppressive activities.
| Product Unit Size | Cost | Quantity | Stock |
|---|
CNX-774 inhibits Bruton’s tyrosine kinase (BTK) and displays potential anticancer and immunosuppressive activities.
| Cas No. | 1202759-32-7 |
|---|---|
| Purity | ≥98% |
| Formula | C26H22FN7O3 |
| Formula Wt. | 499.50 |
| Chemical Name | 4-[4-[[5-fluoro-4-[3-(prop-2-enoylamino)anilino]pyrimidin-2-yl]amino]phenoxy]-N-methylpyridine-2-carboxamide |
| IUPAC Name | 4-[4-[[5-fluoro-4-[3-(prop-2-enoylamino)anilino]pyrimidin-2-yl]amino]phenoxy]-N-methylpyridine-2-carboxamide |
| Synonym | CNX774 |
| Solubility | DMSO 100 mg/mL (200.2 mM) Ethanol 2 mg/mL (4.0 mM) Water Insoluble |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Akinleye A, Chen Y, Mukhi N, et al. Ibrutinib and novel BTK inhibitors in clinical development. J Hematol Oncol. 2013 Aug 19;6:59. PMID: 23958373.
Prolyl hydroxylase inhibitor.
Fluoroquinolone; topoisomerase IV and bacterial...
Endogenous secondary bile acid.
2-methyl-1,4-naphthoquinone derivative
Derivative of aloe-emodin, anthraquinone found ...
Vinca alkaloid found in Catharanthus; microtubu...
PKC and PKD activator, carcinogen.
Mycotoxin derivative; actin polymerization inhi...
Degrader of IKZF1/3
MEK1/2 and Raf inhibitor.
Extract containing catechins and flavonoids fou...
Benzimidazole; microtubule polymerization inhib...
Captothecin derivative; topoisomerase I inhibit...
Coumarin, more potent isomer; VKORC1 inhibitor....
Non-specific caspase inhibitor used to prevent ...
Cyclosporin metabolite; formyl peptide inhibito...
Quinoline; PDE 3B inhibitor.
Macrolide lactone found in Bugula; TLR4 activat...
EZH2 HMT inhibitor.
MGMT inhibitor.