ChemicalBook > CAS DataBase List > CGP77675
CGP77675
- Product Name
- CGP77675
- CAS No.
- 234772-64-6
- Chemical Name
- CGP77675
- Synonyms
- CGP77675;CGP 77675; CGP-77675;CGP77675 >=98% (HPLC);1-(4-(4-Amino-5-(3-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)phenethyl)piperidin-4-ol;1-(2-{4-[4-Amino-5-(3-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]phenyl}ethyl)piperidin-4-ol;4-Piperidinol, 1-[2-[4-[4-aMino-5-(3-Methoxyphenyl)-7H-pyrrolo[2,3-d]pyriMidin-7-yl]phenyl]ethyl]-
- CBNumber
- CB12614668
- Molecular Formula
- C26H29N5O2
- Formula Weight
- 443.54
- MOL File
- 234772-64-6.mol
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CGP77675 Property
- storage temp.
- 2-8°C
- solubility
- DMSO: >10mg/mL
- form
- powder
- color
- white to beige
- InChIKey
- WUPXZZWTHIZICK-UHFFFAOYSA-N
- SMILES
- COc1cccc(c1)-c2cn(-c3ccc(CCN4CCC(O)CC4)cc3)c5ncnc(N)c25
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Safety
- WGK Germany
- 3
- Storage Class
- 11 - Combustible Solids
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N-Bromosuccinimide Price
Sigma-Aldrich
- Product number
- SML0314
- Product name
- CGP77675
- Purity
- ≥98% (HPLC)
- Packaging
- 5mg
- Price
- $174
- Updated
- 2026/03/19
Sigma-Aldrich
- Product number
- SML0314
- Product name
- CGP77675
- Purity
- ≥98% (HPLC)
- Packaging
- 25mg
- Price
- $696
- Updated
- 2026/03/19
Cayman Chemical
- Product number
- 21089
- Product name
- CGP 77675
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $30
- Updated
- 2021/12/16
Cayman Chemical
- Product number
- 21089
- Product name
- CGP 77675
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $113
- Updated
- 2021/12/16
Cayman Chemical
- Product number
- 21089
- Product name
- CGP 77675
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $195
- Updated
- 2021/12/16
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CGP77675 Chemical Properties,Usage,Production
Uses
CGP77675 has been used in the generation of mouse expanded potential stem cells.
General Description
CGP77675 belongs to the pyrrolopyrimidine class of inhibitors.
Biochem/physiol Actions
CGP77675 is a potent Src kinase inhibitor. CGP77675 is selective toward other protein kinases including Cdc2 (>500-fold), epidermal growth factor (EGF) receptor (7.5-fold), vascular endothelial growth factor receptor (>50-fold), and for v-Abl (15-fold) and focal adhesion kinase (Fak) (>25-fold).
in vivo
CGP77675 (1, 5, and 25 mg/kg; injected s.c.; twice a day) inhibits IL-1β-induced hypercalcemia in Mice[1].
CGP77675 (10 and 50 mg/kg; administered orally; twice a day for 6 weeks) partially prevents bone loss and rescues bone microarchitectural features in young ovx rats[1].
| Animal Model: | Male mice (Tif:MAGf; Novartis Animal Farm) of 25-30 g body[1] |
| Dosage: | 1, 5, and 25 mg/kg |
| Administration: | Injected s.c.; twice a day |
| Result: | Prevented IL-1β-induced hypercalcemia in mice without affecting serum amyloid protein levels. |
| Animal Model: | Eight-week-old (175-209 g) female rats of the Sprague-Dawley-derived strain Tif:RAlf[1] |
| Dosage: | 10 and 50 mg/kg |
| Administration: | Administered orally; twice a day for 6 weeks |
| Result: | Partly prevented bone loss. |
CGP77675 Preparation Products And Raw materials
Raw materials
Preparation Products
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