XL177A - 10mM in DMSO , CAS No.2417089-74-6

CAS: 2417089-74-6 Cat. No.: X655412 분자식: C₄₈H₅₇ClN₈O₅ 분자량: 861.47 PubChem CID: 153002269

GRADE & PURITY 10mM in DMSO

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

개요

XL177A is a highly potent and selective irreversible USP7 inhibitor with an IC 50 of 0.34 nM. XL177A elicits cancer cell killing through a p53-dependent mechanism.

In Vitro

XL177A is a potent USP7 inhibitor and p53 stabilizer in cyto. XL177A suppresses cancer cell growth predominantly through a p53-dependent mechanism. XL177A labels the catalytic cysteine, C223, of USP7 with exquisite selectivity for USP7 across the DUBome and human proteome. ?\nXL177A (1 μM) induces complete G1 arrest in MCF7 cells after 24?hours. ?\nTreatment of MCF7 cells, which express WT TP53, with XL177A (0.001- 10 μM) induces rapid degradation of HDM2 within 2?hours, followed by increases in p53 and downstream p21 protein levels. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: MCF7 cells Concentration: 0.001, 0.01, 0.1, 1, 10 μM Incubation Time: 18-24 hours Result: The p53 and p21 protein levels remained high, but MDM2 protein levels matched DMSO control.

Specifications

사양 및 순도

10mM in DMSO

생화학 및 생리적 메커니즘

XL177A is a highly potent and selective irreversible USP7 inhibitor with an IC 50 of 0.34u2009nM. XL177A elicits cancer cell killing through a p53-dependent mechanism.

보관 조건

Store at -80°C

배송

Dry ice packs + Cold packs

이 제품은 콜드 체인 배송이 필요합니다.지상 및 기타 경제 서비스는 사용할 수 없습니다.

이름과 식별자

PubChem CID

153002269

분자량

861.47