RO5126766 (CH5126766)
Catalog No. A14019
RO5126766 (CH5126766)是对Raf和MEK丝裂原激活的蛋白激酶(MAPK)具有特异性的蛋白激酶抑制剂,具有潜在的抗肿瘤活性。
- Yuki Shimizu, .et al. Acquired resistance to BRAF inhibitors is mediated by BRAF splicing variants in BRAF V600E mutation-positive colorectal neuroendocrine carcinoma, Cancer Lett, 2022, Sep 1;543 PMID: 35724767
Catalog Num | A14019 |
---|---|
M. Wt | 471.5 |
Formula | C21H18FN5O5S |
Purity | >98% |
Storage | at -20°C 3 years Powder |
CAS No. | 946128-88-7 |
Synonyms | RO 5126766, RO-5126766, CH5126766, CH-5126766, CH 5126766. |
SMILES | CC1=C(C(=O)OC2=C1C=CC(=C2)OC3=NC=CC=N3)CC4=C(C(=NC=C4)NS(=O)(=O)NC)F |
RO5126766 (CH5126766)是对Raf和MEK丝裂原激活的蛋白激酶(MAPK)具有特异性的蛋白激酶抑制剂,具有潜在的抗肿瘤活性。
Targets
BRAF V600E | BRAF | CRAF | MEK1 | |
8.2 nM | 19 nM | 56 nM | 160 nM |
In vitro (25°C) | DMSO | 93 mg/mL (197.26 mM) | |
Water | Insoluble | ||
Ethanol | Insoluble | ||
In vivo | 5% DMSO+45% PEG 300+ddH2O | 19 mg/mL | |
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.1 mM | 21.21 mL | 106.04 mL | 212.09 mL |
0.5 mM | 4.24 mL | 21.21 mL | 42.42 mL |
1 mM | 2.12 mL | 10.6 mL | 21.21 mL |
5 mM | 0.42 mL | 2.12 mL | 4.24 mL |
*The above data is based on the productmolecular weight 471.5. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.