ChemicalBook > CAS DataBase List > GW441756
GW441756
GW441756
- CAS No.504433-23-2
- Chemical Name:GW441756
- CBNumber:CB1839809
- Molecular Formula:C17H13N3O
- Formula Weight:275.3
- MOL File:504433-23-2.mol
GW441756 Property
- Boiling point 568.0±50.0 °C(Predicted)
- Density 1.31±0.1 g/cm3(Predicted)
- storage temp. Store at RT
- solubility Soluble in DMSO (up to 5 mg/ml).
- pka 11.04±0.20(Predicted)
- form solid
- color Orange
- Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
Safety
-
Symbol(GHS)
- Signal wordWarning
- Hazard statements H302-H315-H319-H335
- Precautionary statements P261-P305+P351+P338
GW441756 Chemical Properties,Usage,Production
- Description GW-441756 (504433-23-2) is a potent and selective TrkA kinase inhibitor (IC50 = 2 nM).
- Uses GW 441756 is an effective Trk binder, a novel bioactive molecule used in the treatment of neuroblastoma in infants.
- Definition ChEBI: 3-[(1-methyl-3-indolyl)methylidene]-1H-pyrrolo[3,2-b]pyridin-2-one is a member of indoles.
- Biological Activity Potent, selective inhibitor of the NGF receptor tyrosine kinase A (TrkA) (IC 50 = 2 nM). Displays > 100-fold selectivity over a range of other kinases.
- storage Store at RT
- References 1) Wood et al. (2004) Discovery and in vitro evaluation of potent TrkA kinase inhibitors: oxindole and aza-oxindoles. Bioorg. Med. Chem. Lett. 14 953 2) Takemoto et al. (2015) Neuroprotection elicited by nerve growth factor and brain-derived neurotrophic factor released from astrocytes in response to methylmercury; Environ. Toxicol. Pharmacol. 40 199 [Focus Citation]
GW441756 Preparation Products And Raw materials
Raw materials
Preparation Products
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504433-23-2, GW441756Related Search:
- QNZ (EVP4593) Bosutinib PF 573228 BAY 87-2243 Raltitrexed Tie2 kinase inhibitor GW284543 GW788388 GW9662 GW5074 GW 284543 hydrochloride - UNC 10225170 hydrochloride 5-[3-Methoxy-4-(4-methoxy-benzyloxy)-benzyl]-pyrimidine-2,4-diamine GW9508 2,4-Thiazolidinedione, 5-[[5-[6-(4-acetyl-1-piperazinyl)-3-nitro-2-pyridinyl]-2-fluorophenyl]methylene]- 1756-L71 1756-OF4 GW441756 1,3-Dihydro-2H-pyrrolo[3,2-b]pyridin-2-one
- Inhibitors
- Angiogenesis and Metastasis
- 药靶配体
- 抑制剂
- 细胞生物学试剂
- 小分子抑制剂,天然产物
- 蛋白酪氨酸激酶
- 504433-23-3
- 化合物GW 441756,10 MM DMSO 溶液
- GW-441756 HYDROCHLORIDE,TRKA RECEPTOR TYROSINE KINASE抑制剂
- GW441756,TRKA受体酪氨酸激酶抑制剂
- TRKA抑制剂(GW 441756)
- 1,3-二氢-3-[(1-甲基-1H-吲哚-3-基)亚甲基]-2H-吡咯并[3,2-B]吡啶-2-酮
- 504433-23-2
- GW 441756, 10 mM in DMSO
- GW 441756/GW 441758
- GW-441756 hydrochloride, TrKA receptor tyrosine kinase inhibitor
- GW441758
- 3-((1-methyl-1H-indol-3-yl)methylene)-1,3-dihydro-2H-pyrrolo[3,2-b]pyridin-2-one
- GW441756 USP/EP/BP
- W 441756
- GW441756, >98%
- CS-1085
- GW 441756; GW-441756
- 3-[(1-METHYLINDOL-3-YL)METHYLIDENE]-1H-PYRROLO[3,2-B]PYRIDIN-2-ONE;HYDROCHLORIDE
- 3-[(1-methylindol-3-yl)methylidene]-1H-pyrrolo[3,2-b]pyridin-2-one
- -3-((1-methyl-1H-indol-3-yl)methylene)-1H-pyrrolo[3,2-b]pyridin-2(3H)-one
- (Z)-3-((1-methyl-1H-indol-3-yl)methylene)-1H-pyrrolo[3,2-b]pyridin-2(3H)-one
- 2H-Pyrrolo[3,2-b]pyridin-2-one, 1,3-dihydro-3-[(1-methyl-1H-indol-3-yl)methylene]-
- Gw
- GW 441756
- 1,3-DIHYDRO-3-[(1-METHYL-1H-INDOL-3-YL)METHYLENE]-2H-PYRROLO[3,2-B]PYRIDIN-2-ONE