A66

Item no.	S2636-5
Manufacturer	Selleckchem
CASRN	1166227-08-2
Amount	5 mg
Quantity options	10 mg 100 mg 1 g 10 g 10 mM/1 ml 200 mg 5 mg 50 mg 5 g
Category	Neuroscience Metabolism Diabetes Cholesterol & Lipid Metabolism Regulation of Appetite Neural Signaling Inhibitors & Compound Libraries Small Molecules
Type	Inhibitors
Specific against	other
Smiles	CC1=C(SC(=N1)NC(=O)N2CCCC2C(=O)N)C3=CSC(=N3)C(C)(C)C
ECLASS 10.1	32160490
ECLASS 11.0	32160490
UNSPSC	12000000
Alias	1166227-08-2 '
Similar products	A66
Available
Manufacturer - Targets	PI3K
Storage Conditions	2 years -80 in solvent
Molecular Weight	393, 53
Administration	Intraperitoneal injection
Animal Models	Age-matched specific pathogen-free Rag1-/- or NIH-III mice inoculated subcutaneously with U87MG, SK-OV-3 or HCT-116 cells
Dosages	100 mg/kg once daily (QD) or 75 mg/kg twice daily (BID)
Formulation	Formulated in 20% 2-hydroxypropyl-beta-cyclodextrin in water
IC50	32 nM [1], 32 nM [1], 32 nM [1], 32 nM [1], 32 nM [1], 32 nM [1]
In vitro	In addition to the wild-type p110alpha, A66 also potently inhibits the oncogenic forms of p110alpha such as p110alpha E545K and p110alpha H1047R with IC50 of 30 nM and 43 nM, respectively. Unlike PIK-75, A66 displays >100 fold selectivity for p110alpha over other class-I PI3K isoforms. Among the class-II PI3Ks, class-III PI3K and PI4Ks, A66 only exhibits limited cross-reactivity with the class-II PI3K PI3KC2beta and the PI4Kbeta isoform of PI4K with IC50 of 462 nM and 236 nM, respectively. A66 exhibits no inhibitory activity against other lipid kinases or the related kinases DNA-PK and mTOR. A66 has a higher degree of specificity compared with PIK-75 when tested at 10 uM against two large panels of 110 protein kinases and 318 kinases. Inhibition of p110alpha alone by A66 treatment is sufficient to block insulin signalling to Akt/PKB in certain cell lines that harbor H1047R mutations in PIK3CA and have high levels of p110alpha and class-Ia PI3K activity. [1] A66 treatment at 0.7 uM induces a 75-80% reduction in focus formation by the highly transforming p85alpha iSH2 mutants KS459delN, DKRMN-S560del, and K379E, and reduces the phosphorylation of Akt on T308 by all p85 mutants. [2]
In vivo	A single dose of A66 at 100 mg/kg induces a profound reduction in the phosphorylation of Akt/PKB and p70 S6 kinase, but not of ERK, in SK-OV-3 tumour tissue in vivo at both 1 hour and 6 hours after dosing. A66 dosed at 100 mg/kg once daily (QD) for 21 days or 75 mg/kg twice daily (BID) for 16 days induces a significant delay in growth of SK-OV-3 xenografted tumors with average TGI of 45.9% and 29.9%, respectively, which is even greater than that induced by the well-established pan-PI3K inhibitor BEZ-235. QD dosing of A66 in the HCT-116 xenograft model also induces a significant reduction in tumour volume with TGI of 77.2%, but causes a non-significant reduction in tumor volume in the U87MG xenograft model. [1] Administration of A66 at 10 mg/kg in male CD1 mice induces significant impairments in the ITT (insulin tolerance test) and GTT (glucose tolerance test), and an increase in glucose production during a PTT (pyruvate tolerance test), almost to the same level as the pan-PI3K inhibitors. [3]
Kinase Assay	PI3K (human) HTRF Assay, The p110alpha isoform is produced in-house by co-expressing full-length human p85alpha with the indicated human full-length catalytic subunit containing a histidine tag at the N-terminus to allow purification. The p110alpha is titrated and used at a concentration between EC65-EC80 values. IC50 value is evaluated using the PI3K (human) HTRF Assay.
Solubility (25C)	DMSO 79 mg/mL, Water <1 mg/mL, Ethanol 1 mg/mL
Information	A66 is a potent and specific p110α inhibitor with IC50 of 32 nM in a cell-free assay, >100 fold selectivity for p110α over other class-I PI3K isoforms.
Chemical Name	(2S)-N1-(5-(2-tert-butylthiazol-4-yl)-4-methylthiazol-2-yl)pyrrolidine-1, 2-dicarboxamide
Features	A66 is highly selective for p110alpha isoform.

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