For research use only. Not for therapeutic Use.
<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">N-Deshydroxyethyl Dasatinib (CAS 910297-51-7) is a metabolite of Dasatinib. It is used in the treatment of cancers and immune diseases. </span></span></span><span style="color: rgb(0, 0, 0); font-family: arial, helvetica, sans-serif;">Dasatinib is a </span><span style="color: rgb(0, 0, 0); font-family: "Helvetica Neue", Helvetica, Arial, sans-serif;">Bcr-abl tyrosine kinase inhibitor and an </span><span style="color: rgb(0, 0, 0); font-family: "Helvetica Neue", Helvetica, Arial, sans-serif;">EphA2 receptor antagonist.</span>
Catalog Number | R008570 |
CAS Number | 910297-51-7 |
Synonyms | N-(2-Chloro-6-methylphenyl)-2-[[2-methyl-6-(1-piperazinyl)-4-pyrimidinyl]amino]-5-thiazolecarboxamide; Dasatinib metabolite M4; |
Molecular Formula | C20H22ClN7OS |
Purity | ≥95% |
Target | Drug Metabolite |
Storage | Store at -20°C |
Overview of Clinical Research | <span style="color:#000000;"><span style="font-size:12px;"><span style="font-family: arial, helvetica, sans-serif;">Dasatinib is a </span><span style="font-family: "Helvetica Neue", Helvetica, Arial, sans-serif;">Bcr-abl tyrosine kinase inhibitor and an </span><span style="font-family: "Helvetica Neue", Helvetica, Arial, sans-serif;">EphA2 receptor antagonist. It has been granted for thr orphan drug status in </span><span style="font-family: "Helvetica Neue", Helvetica, Arial, sans-serif;">Chronic myeloid leukaemia and Precursor cell lymphoblastic leukaemia-lymphoma. </span><span style="font-family: "Helvetica Neue", Helvetica, Arial, sans-serif;">Bristol-Myers Squibb and the M.D. Anderson Cancer Center completed a phase I/II trial in Breast cancer (Combination therapy, Metastatic disease, Second-line therapy or greater) in USA (NCT00566618) in Nov, 2020. </span></span></span> |
IUPAC Name | N-(2-chloro-6-methylphenyl)-2-[(2-methyl-6-piperazin-1-ylpyrimidin-4-yl)amino]-1,3-thiazole-5-carboxamide |
InChI | InChI=1S/C20H22ClN7OS/c1-12-4-3-5-14(21)18(12)27-19(29)15-11-23-20(30-15)26-16-10-17(25-13(2)24-16)28-8-6-22-7-9-28/h3-5,10-11,22H,6-9H2,1-2H3,(H,27,29)(H,23,24,25,26) |
InChIKey | DOBZFFWLHXORTB-UHFFFAOYSA-N |
SMILES | CC1=C(C(=CC=C1)Cl)NC(=O)C2=CN=C(S2)NC3=NC(=NC(=C3)N4CCNCC4)C |
Reference | <span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.Trentham, D. R., et al. "Elementary processes of the magnesium ion-dependent adenosine triphosphatase activity of heavy meromysin. A transient kinetic approach to the study of kinases and adenosine triphosphatases and a colorimetric inorganic phosphate assay in situ." <i style="font-family: Arial, sans-serif; font-size: 13px;">Biochemical Journal</i> 126.3 (1972): 635-644.<br /> |