[CAS NO. 2999763-09-4]  VT02956

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PRODUCTS SPECIFICATIONS [2999763-09-4]

Catalog
HY-147165
Brand
MCE
CAS
2999763-09-4

DESCRIPTION [2999763-09-4]

Overview

MDL-
Molecular Weight373.45
Molecular FormulaC22H23N5O
SMILESNCC1CCN(CC1)C2=NC(C3=CC=NC=C3)=NC4=C2C=CC=C4C#CCO

For research use only. We do not sell to patients.

Summary

VT02956 is a LATS inhibitor ( IC 50 : 0.76 nM for LATS1, 0.52 nM for LATS2). VT02956 targets the Hippo pathway. VT02956 inhibits ESR1 expression and growth of ER+ breast cancer cell lines and patient-derived tumor organoids [1] .


IC50 & Target

IC50: 0.76 nM for LATS1, 0.52 nM for LATS2 [1]


In Vitro

VT02956 (2 μM, 0-30 min) reduces YAP/TAZ phosphorylation in HEK293A cells and 4T1 cells [1] .
VT02956 (2 μM, 2 days) reduces ERα and its target genes TFF1 and GREB1 in breast tumor organoids BTO-02 [1] .
VT02956 (2 μM, 4 days) inhibits the proliferation of ER+ breast cancer cells, such as MCF-7 and T47D cells [1] .
VT02956 (2 μM, 7 days) dramatically reduces MCF-7 growth when combined with Palbociclib (HY-50767) (0.1 and 0.3 μM) [1] .
VT02956 (2 μM, 9 days) results in a much more drastic reduction in colony formation of MCF-7 cells when combined with Palbociclib (HY-50767) (0.1 μM) [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay [1]

Cell Line: MCF-7 and T47D cells
Concentration: 2 μM
Incubation Time: 4 days
Result: Inhibited the proliferation of ER+ breast cancer cells by targeting the LATS-YAP/TAZ-ERα.

Western Blot Analysis [1]

Cell Line: HEK293A cells and 4T1 cells
Concentration: 2 μM
Incubation Time: 0-30 min
Result: Inhibited YAP/TAZ phosphorylation with IC 50 s of 0.16 μM and 0.43 μM respectively.

Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Please store the product under the recommended conditions in the Certificate of Analysis.