ETP-46321

Modify Date: 2024-01-08 16:17:46

ETP-46321 Structure
ETP-46321 structure
Common Name ETP-46321
CAS Number 1252594-99-2 Molecular Weight 473.55200
Density N/A Boiling Point N/A
Molecular Formula C20H27N9O3S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of ETP-46321


ETP-46321 is a potent and orally bioavailable PI3Kα and PI3Kδ inhibitor with Kiapps of 2.3 and 14.2 nM, respectively.

 Names

Name 5-(2-((4-methylsulfonylpiperazin-1-yl)methyl)-8-morpholinoimidazo[1,2-a]pyrazin-6-yl)pyrimidin-2-amine
Synonym More Synonyms

 ETP-46321 Biological Activity

Description ETP-46321 is a potent and orally bioavailable PI3Kα and PI3Kδ inhibitor with Kiapps of 2.3 and 14.2 nM, respectively.
Related Catalog
Target

p110α:2.3 nM (Ki)

PI3Kα-E545K:1.77 nM (Ki)

PI3Kα-E542K:1.89 nM (Ki)

PI3Kα-H1047R:2.33 nM (Ki)

p110δ:14.2 nM (Ki)

p110β:170 nM (Ki)

p110γ:179 nM (Ki)

In Vitro ETP-46321 is selected to be screened against other PI3K isoforms. ETP-46321 is more potent against isoform α (Kiapp=2.3 nM). ETP-4632, has been profiled and shown to be a potent PI3K α and δ inhibitor, highly selective versus mTOR and 288 representative kinases. ETP-46321 is also tested against three of the p110α mutant enzymes detected in human cancers (E542K, E545K and H1047R), being equipotent against these mutants when compared to the wild type protein (Kiapp=2.33, 1.77 and 1.89 nM for PI3Kα-H1047R, PI3Kα-E545K and PI3Kα-E542K, respectively). ETP-46321 inhibits the phosphorilation of AKT in U2OS cell line with an IC50 of 8.3 nM[1].
In Vivo ETP-46321, is selected for in vivo studies based on its appealing pharmacokinetic profile in BALB-C mice, low in vivo Clearance (0.6 L/h/Kg) and good oral bioavailability (90%). ETP-46321 demonstrates a good pharmacokinetic profile in mice and is selected for preliminary in vivo evaluation in a lung tumor mouse model driven by a K-RasG12V oncogenic mutation, showing significant tumor growth inhibition, and reduction of the tumor metabolic activity as measured by positron emission tomography (PET) techniques[1].
Animal Admin Mice[1] BALB/C mice are treated daily with ETP-46321 (50 mg/kg, p.o.) for three weeks. Tumor volumes of four mice in each treatment group are measured and compared to the starting volume at the beginning of the treatment.
References

[1]. Martínez González S, et al. Identification of ETP-46321, a potent and orally bioavailable PI3K α, δ inhibitor. Bioorg Med Chem Lett. 2012 May 15;22(10):3460-6.

 Chemical & Physical Properties

Molecular Formula C20H27N9O3S
Molecular Weight 473.55200
Exact Mass 473.19600
PSA 143.46000
LogP 1.28510
Storage condition 2-8℃

 Synonyms

5-(2-((4-sulfonylmethylpiperazin-1-yl)methyl)-8-morpholinoimidazo[1,2-a]pyrazin-6-yl)pyrimidin-2-amine
ETP-46321
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Price: $462/10mM*1mLinDMSO

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