Pictilisib
Cat.No:IP1360 Solarbio
CAS:957054-30-7
Molecular Formula:C23H27N7O3S2
Molecular Weight:513.64
Storage:Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:HPLC≥98%
Appearance:Off-white to yellow Solid
Qty:
Size:
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My Cart> Small Molecule Compounds > Inhibitors & Antagonists & Agonists > PI3K/Akt/mTOR > PictilisibCAS:957054-30-7
Molecular Formula:C23H27N7O3S2
Molecular Weight:513.64
Storage:Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year
Purity:HPLC≥98%
Appearance:Off-white to yellow Solid
Qty:
Size:
| CAS | 957054-30-7 |
| Name | Pictilisib |
| Molecular Formula | C23H27N7O3S2 |
| Molecular Weight | 513.64 |
| Solubility | Soluble in DMSO |
| Purity | HPLC≥98% |
| Appearance | Off-white to yellow Solid |
| Storage | Powder:2-8℃,2 years;Insolvent(Mother Liquid):-20℃,6 months;-80℃,1 year |
| EC | EINECS 1312995-182-4 |
| MDL | MFCD11616196 |
| SMILES | CS(N1CCN(CC2=CC3=C(C(N4CCOCC4)=NC(C5=CC=CC6=C5C=NN6)=N3)S2)CC1)(=O)=O |
| Target Point | PI3K |
| Passage | PI3K/Akt/mTOR |
| Background | GDC-0941 is a potent PI3Kα/δ inhibitor. |
| Biological Activity | GDC-0941 是有效的 PI3Kα/δ 抑制剂, IC50为 3 nM; 对110β (11倍) 和 p110γ (25倍) 具有适度的选择性[1-7]。 |
| IC50 | p110α:3nM (IC50) p110α-H1047R:3nM (IC50) p110α-E545K:3nM (IC50) p110δ:3nM (IC50) p110β:33nM (IC50) p110γ:75nM (IC50)mTOR:0.58μM (Ki) DNA-PK:1.23μM (IC50) [1-7] |
| Data Literature Source | [1]. Wallin JJ, et al. GDC-0941, a novel class I selective PI3K inhibitor, enhances the efficacy of docetaxel in human breast cancer models by increasing cell death in vitro and in vivo.Clin Cancer Res. 2012 Jul 15; 18 (14) :3901-11. Epub 2012 May 14. [2]. Wullschleger S, et al. Quantitative MRI establishes the efficacy of PI3K inhibitor (GDC-0941) multi-treatments in PTEN-deficient mice lymphoma.Anticancer Res. 2012 Feb; 32 (2) :415-20. [3]. Zou ZQ, et al. The novel dual PI3K/mTOR inhibitor GDC-0941 synergizes with the MEK inhibitor U0126 in non-small cell lung cancer cells.Mol Med Report. 2012 Feb; 5 (2) :503-8. [4]. Burrows N, et al. GDC-0941 inhibits metastatic characteristics of thyroid carcinomas by targeting both the phosphoinositide-3 kinase (PI3K) and hypoxia-inducible factor-1α (HIF-1α) pathways.J Clin Endocrinol Metab. 2011 Dec; 96 (12) :E1934-43. Epub 2011 Oct [5]. Folkes AJ, et al. The identification of 2- (1H-indazol-4-yl) -6- (4-methanesulfonyl-piperazin-1-ylmethyl) -4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer . J Med Chem. 2008 Sep 25; 51 (18) :5522-32. [6]. Ni J, et al. Functional characterization of an isoform-selective inhibitor of PI3K-p110β as a potential anticancer agent. Cancer Discov. 2012 May; 2 (5) :425-33. [7]. Cheng H, et al. A genetic mouse model of invasive endometrial cancer driven by concurrent loss of Pten and Lkb1 Is highly responsive to mTOR inhibition. Cancer Res. 2014 Jan 1; 74 (1) :15-23. |
| Unit | Bottle |
| Specification | 10mg 50mg 100mg |
Remark:These protocols are for reference only. Solarbio does not independently validate these methods.
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