PI3K/VEGFR2-IN-1

SKU:BHB21901543
Overview
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PI3K/VEGFR2-IN-1 (CAS 2851067-08-6) is an inhibitor. Reported to act on PI3K, VEGFR2. Relevant to PI3K/Akt/mTOR and Protein Tyrosine Kinase/RTK research. Molecular formula C17H14ClN3OS, molecular weight 343.83 g/mol.
CAS Number 2851067-08-6
Molecular Weight 343.83 g/mol
Target PI3K, VEGFR2
Storage See Certificate of Analysis
Options selector
Catalog no. Size
HY-151635-50MG 50 mg
HY-151635-100MG 100 mg
HY-151635-250MG 250 mg
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  • Storage: Please store the product under the recommended conditions in the Certificate of Analysis.
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Field Specification
Target PI3K, VEGFR2
CAS no. 2851067-08-6
Applications
  • Functional Assay (In Vitro)
Molecular weight 343.83
Molecular formula C17H14ClN3OS
SMILES S=C(N/N=C(C1=CC2=CC=CC=C2O1)\C)NC3=CC=C(Cl)C=C3
Storage Refer to Certificate of Analysis (CoA) for storage conditions
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-151635
Main SKU BHB21901543
Inhibitors

Compound Overview

PI3K/VEGFR2-IN-1 is a potent dual inhibitor of PI3K and VEGFR2, with IC50 values of 2.21 μM and 68 μM, respectively. It induces apoptosis and can be used in cancer research[1]. Its molecular formula is C17H14ClN3OS, with a molecular weight of 343.83 g/mol.

Physical & Chemical Properties

CAS Number 2851067-08-6
Molecular Formula C17H14ClN3OS
Molecular Weight 343.83 g/mol
SMILES S=C(N/N=C(C1=CC2=CC=CC=C2O1)\C)NC3=CC=C(Cl)C=C3
Target PI3K, VEGFR2
Signaling Pathway PI3K/Akt/mTOR; Protein Tyrosine Kinase/RTK; Apoptosis
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Shipping Room temperature in continental US; may vary elsewhere.

Biological Activity

IC50 & Target[1]

PI3K

2.21 μM (IC50)

VEGFR2

68 μM (IC50)

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. El-Khouly OA, et al. Design, synthesis and computational study of new benzofuran hybrids as dual PI3K/VEGFR2 inhibitors targeting cancer. Sci Rep. 2022 Oct 12;12(1):17104.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with your institution's chemical hygiene plan.

In Vitro

In HePG2, MCF-7, Hela, and PC3 cells, PI3K/VEGFR2-IN-1 at 1.56-100 μM for 24 h inhibits cell proliferation in a dose-dependent manner[1]. In MCF-7 and Hela cells, PI3K/VEGFR2-IN-1 (10 mg/mL; 24 h) arrests the cell cycle at G1/S phase and induces apoptosis[1].

Cell Viability Assay[1]

Cell LineHePG2, MCF-7, Hela, and PC3 cells
Concentration1.56-100 μM
Incubation Time24 hours
ResultHad antitumor activity with IC50 values of 7.94, 9.73, 11.58, and 17.49 μM for Hela, HePG2, MCF-7 and PC3 cells, respectively.

Cell Cycle Analysis[1]

Cell LineMCF-7 cells
Concentration10 mg/mL
Incubation Time24 hours
ResultArrested cell cycle in G1/S phase at 24 h by 51.23%.

Cell Cycle Analysis[1]

Cell LineMCF-7 and Hela cells
Concentration10 mg/mL
Incubation Time24 hours
ResultEnhanced late apoptotic induction with 14.11% at Hela cells.

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price listed?
A.Every size of this product is quoted on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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