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BLU-667
- Pralsetinib - RG 6396- Optical Purity: Optically pure
- Soluble in DMSO and EtOH
- MF: C27H32FN9O2
- MW: 533.6
Description
BLU-667 is a highly potent and selective RET inhibitor with an IC50 value of 0.4 nM. In vivo, BLU-667 potently inhibited growth of NSCLC and thyroid cancer xenografts driven by various RET mutations and fusions without inhibiting VEGFR2.
More Information
| Parent CAS No. | 2097132-94-8 |
|---|---|
| Chemical Name | (1s,4R)-N-((S)-1-(6-(4-fluoro-1H-pyrazol-1-yl)pyridin-3-yl)ethyl)-1-methoxy-4-(4-methyl-6-(5-methyl-1H-pyrazol-3-ylamino)pyrimidin-2-yl)cyclohexanecarboxamide |
| SMILES | C1(C)C=C(NC2C=C(C)NN=2)N=C([C@@H]2CC[C@@](OC)(C(=O)N[C@@H](C)C3C=NC(N4C=C(F)C=N4)=CC=3)CC2)N=1 |&1:13,16,22,r| |
| MFCD | N.A. |
| InChi | InChI=1S/C27H32FN9O2/c1-16-11-22(33-23-12-17(2)35-36-23)34-25(31-16)19-7-9-27(39-4,10-8-19)26(38)32-18(3)20-5-6-24(29-13-20)37-15-21(28)14-30-37/h5-6,11-15,18-19H,7-10H2,1-4H3,(H,32,38)(H2,31,33,34,35,36)/t18-,19?,27?/m0/s1 |
| InChiKey | GBLBJPZSROAGMF-SIYOEGHHSA-N |
| CID | 129073603 |
| Short Description | RET inhibitor |
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