>>Signaling Pathways>> TGF-β / Smad Signaling>> TGF-β Receptor>>LY3200882

LY3200882

Catalog No.GC19234

LY3200882는 IC50이 38.2nM인 강력하고 고도로 선택적인 ATP 경쟁적 경구 활성 TGF-β 수용체 유형 1(ALK5) 억제제입니다.

Products are for research use only. Not for human use. We do not sell to patients.

LY3200882 Chemical Structure

Cas No.: 1898283-02-7

Size 가격 재고 수량
5mg
US$111.00
재고 있음
10mg
US$176.00
재고 있음
50mg
US$603.00
재고 있음
100mg
US$1,020.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

LY3200882 is a novel and highly selective inhibitor of TGF-β receptor type 1 (TGFβRI).

LY3200882 is a novel, highly selective inhibitor of TGF-β receptor type 1 (TGFβRI). LY3200882 potently inhibits TGFβ mediated SMAD phosphorylation in vitro in tumor and immune cells. LY3200882 has shown anti-metastatic activity in vitro in migration assays. In in vitro immune suppression assays, LY3200882 has shown the ability to rescue TGFβ1 suppressed or T regulatory cell suppressed naive T cell activity and restore proliferation[1].

LY3200882 potently inhibits TGFβ mediated SMAD phosphorylation in vivo in subcutaneous tumors in a dose dependent fashion. LY3200882 has shown anti-metastatic activity in vivo in an experimental metastasis tumor model (intravenous EMT6-LM2 model of triple negative breast cancer)[1].

References:
[1]. Huaxing Pei, et al. Abstract 955: LY3200882, a novel, highly selective TGFβRI small molecule inhibitor. AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 955.

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Average Rating: 5 ★★★★★ (Based on Reviews and 16 reference(s) in Google Scholar.)

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