GNE-490
- Product Name
- GNE-490
- CAS No.
- 1033739-92-2
- Chemical Name
- GNE-490
- Synonyms
- GNE-490;CS-2657;GNE490;GNE 490;GNE-490, 10 mM in DMSO;2-(2-(2-amino-4-methylpyrimidin-5-yl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)propan-2-ol;2-[2-(2-amino-4-methylpyrimidin-5-yl)-4-(morpholin-4-yl)thieno[3,2-d]pyrimidin-6-yl]propan-2-ol;Thieno[3,2-d]pyrimidine-6-methanol, 2-(2-amino-4-methyl-5-pyrimidinyl)-α,α-dimethyl-4-(4-morpholinyl)-;2-(2-Amino-4-methyl-5-pyrimidinyl)-alpha,alpha-dimethyl-4-(4-morpholinyl)thieno[3,2-d]pyrimidine-6-methanol;PI3Kβ,GNE 490,PI3Kδ,Mammalian target of Rapamycin,mTOR,GNE-490,MCF7.1,PI3K,PI3Kα,Phosphoinositide 3-kinase,PI3Kγ,breast cancer,Inhibitor,GNE490,inhibit
- CBNumber
- CB92621136
- Molecular Formula
- C18H22N6O2S
- Formula Weight
- 386.47
- MOL File
- 1033739-92-2.mol
GNE-490 Property
- storage temp.
- 4°C, protect from light
- solubility
- DMSO : ≥ 100 mg/mL (258.75 mM)
- form
- Solid
- color
- White to off-white
N-Bromosuccinimide Price
- Product number
- KIN0001422
- Product name
- GNE-490
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $500.76
- Updated
- 2021/12/16
- Product number
- SYN1114
- Product name
- GNE-490
- Packaging
- 10mg
- Price
- $560
- Updated
- 2021/12/16
- Product number
- SYN-1114-M010
- Product name
- GNE-490
- Purity
- ≥95%
- Packaging
- 10mg
- Price
- $583
- Updated
- 2021/12/16
- Product number
- DC8502
- Product name
- GNE-490
- Purity
- >98%
- Packaging
- 100mg
- Price
- $800
- Updated
- 2021/12/16
- Product number
- DC8502
- Product name
- GNE-490
- Purity
- >98%
- Packaging
- 250mg
- Price
- $1500
- Updated
- 2021/12/16
GNE-490 Chemical Properties,Usage,Production
Description
GNE-490 is a highly selective pan-PI3K inhibitor, demonstrating selectivity over mTOR.
Uses
GNE-490, a (thienopyrimidin-2-yl)aminopyrimidine, is a potent pan-PI3K inhibitor with IC50s of 3.5 nM, 25 nM, 5.2 nM, 15 nM for ?PI3Kα, PI3Kβ, PI3Kδ and PI3Kγ, respectively. GNE-490 has >200 fold selectivity for mTOR (IC50=750 nM). GNE-490 shows potent suppression efficacy profile against MCF7.1 breast cancer xenograft model[1].
IC 50
PI3Kα: 3.5 nM (IC50); PI3Kβ: 25 nM (IC50); PI3Kδ: 5.2 nM (IC50); PI3Kγ: 15 nM (IC50); mTOR: 750 nM (IC50)
References
[1] Daniel P Sutherlin, et al. Discovery of (thienopyrimidin-2-yl)aminopyrimidines as potent, selective, and orally available pan-PI3-kinase and dual pan-PI3-kinase/mTOR inhibitors for the treatment of cancer. J Med Chem. 2010 Feb 11;53(3):1086-97. DOI:10.1021/jm901284w
GNE-490 Preparation Products And Raw materials
Raw materials
Preparation Products
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