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            目錄:MedChemExpress LLC>>生化試劑>> H3B-6545 | MCE

            H3B-6545 | MCE
            • H3B-6545 | MCE
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            更新時間:2023-06-20 09:35:43瀏覽次數(shù):261評價

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            CAS 2052130-80-8 純度 ≥99.0%
            分子量 567.58 分子式 C??H??F?N?O?
            供貨周期 現(xiàn)貨 規(guī)格 5 mg
            貨號 HY-112596 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥/生物制藥
            H3B-6545 | MCEH3B-6545 is an oral, selective <b>estrogen receptor</b> covalent antagonist (<b>SERCA</b>) for the research of metastatic ER-positive, HER2-negative breast cancer<sup>[1]</sup><sup>[2]</sup>.

            MCE 的所有產(chǎn)品僅用作科學研究或藥證申報,我們不為任何個人用途提供產(chǎn)品和服務(wù)。

            H3B-6545

            CAS No. : 2052130-80-8

            產(chǎn)品活性:H3B-6545 is an oral, selective estrogen receptor covalent antagonist (SERCA) for the research of metastatic ER-positive, HER2-negative breast cancer.

            研究領(lǐng)域:Vitamin D Related/Nuclear Receptor

            作用靶點:Estrogen Receptor/ERR

            In Vitro: H3B-6545 is a highly selective small molecule that potently antagonizes wild-type and mutant ERα in biochemical and cell based assays. In vitro comparisons with standard of care and other experimental agents confirm increased cell potency of H3B-6545 under continuous as well as washout treatment conditions. H3B-6545, a member of a novel class of ERα antagonists refer to as selective ER covalent antagonist (SERCA), which inactivates both wild-type and mutant ERα by targeting C530 and enforcing a unique antagonist conformation. H3B-6545 is a first-in-class selective ER covalent antagonist (SERCA). H3B-6545 inhibits ERαWT activity and growth of ERαWT -positive breast cancer lines. H3B-6545 potently inhibits ERαWT activity and suppresses proliferation of ERαWT -positive breast cancer lines. With GI50s of 0.3-0.4, 1.0, 0.5, 5.2, and 0.2 nM for MCF7, HCC1428, BT483, T47D and CAMA-1 cell lines.

            In Vivo: In vivo, once daily oral dosing of H3B-6545 shows potent activity and superior efficacy to fulvestrant in the MCF-7 xenograft model with maximal antitumor activity at doses >10x below the maximum tolerated dose in mice. In addition, H3B-6545 shows superior antitumor activity to Tamoxifen and Fulvestrant in patient derived xenograft models of estrogen receptor positive breast cancer including models carrying ERα mutations in rat and monkeys, H3B-6545 is well tolerated across a broad dose range and at exposures that significantly exceed those required for efficacy in mouse xenograft models.

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