Structure Info
- Chemspace ID
- CSCS20620707475 (Synthesis)
- IUPAC Name
- methyl (1s,2R,3R,4S,5S,6s,7R,8s)-8-(4-{1-[4-({3-carbamoyl-5-ethyl-6-[(oxan-4-yl)amino]pyrazin-2-yl}amino)-2-methoxyphenyl]piperidin-4-yl}piperazine-1-carbonyl)cubane-1-carboxylate
- Mol formula
- C39H50N8O6
- Mol weight
- 727 Da
- Catalog Number(s)
- HY-168741
- Copy structure to query editor
- SMILES
- INCHI
- INCHI key
- MOL
Properties
- LogP
- 1.81
- Heavy atoms count
- 53
- Rotatable bond count
- 12
- Number of rings
- 10
- Carbon bond saturation, Fsp3
- 0.666
- Polar surface area (Å)
- 164
- Hydrogen bond acceptors count
- 11
- Hydrogen bond donors count
- 3
- Zoom the structure
- CSCS20620707475
Items Overall 2 items from 2 suppliers
| Supplier | Lead time | Ships from | Purity | Pack | Price, € | Qty |
|---|---|---|---|---|---|---|
| MedChemExpress | TBD | United States To: | 90 | 1 mg | POA | |
Description: Names: FLT3-ITD-IN-2; Product Description: FLT3-ITD-IN-2 (Compound A1) is an inhibitor for FLT3-ITD kinase with an IC 50 of 2.12 nM. FLT3-ITD-IN-2 inhibits the proliferation of FLT3-dependent human AML cell line MOLM-13 with an IC 50 of 25.65 nM. FLT3-ITD-IN-2 exhibits antitumor efficacy against acute myeloid leukemia .; Target: FLT3 | ||||||
| MedChemExpress EU | TBD | Sweden To: | 90 | 1 mg | POA | |
Description: Names: FLT3-ITD-IN-2; Product Description: FLT3-ITD-IN-2 (Compound A1) is an inhibitor for FLT3-ITD kinase with an IC50 of 2.12 nM. FLT3-ITD-IN-2 inhibits the proliferation of FLT3-dependent human AML cell line MOLM-13 with an IC50 of 25.65 nM. FLT3-ITD-IN-2 exhibits antitumor efficacy against acute myeloid leukemia; Target: FLT3 | ||||||
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