1. PROTAC Epigenetics
  2. Epigenetic Reader Domain PROTACs
  3. SMD-3236

SMD-3236 是基于 SMARCA 配体和 VHL-1 配体设计的、靶向 SMARCA2 的PRAOTAC 降解剂,具有体内长效抗肿瘤活性。SMARCA2 是具有 SMARCA4 缺陷癌细胞中的合成致死靶点,SMD-3236 对 SMARCA2 的降解选择性是 SMARCA4 的 2000 倍,DC50< 1 nM,Dmax>95%。SMD-3236 可诱导肿瘤组织的 SMARCA2 缺失,同时保留 SMARCA4蛋白,在 H838 smarca4 缺陷人类癌症异种移植模型中,抑制肿瘤生长。SMD-3236 由靶蛋白配体 (red part) SMI-1074 (HY-170817),PROTAC linker (black part) (trans-4-Ethynylcyclohexyl)methyl methanesulfonate (HY-170825),E3 连接酶配体 (blue part) SMARCA2 ligand-14 (HY-170826) 组成,其中 E3 连接酶配体和 linker 组成偶联物 E3 Ligase Ligand-linker Conjugate 159 (HY-170827)。

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SMD-3236 Chemical Structure

SMD-3236 Chemical Structure

CAS No. : 3033586-31-8

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  • 生物活性

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生物活性

SMD-3236 is a SMARCA2-targeted PRAOTAC degrader designed based on SMARCA ligands and VHL-1 ligands, with long-lasting antitumor activity in vivo. SMARCA2 is a synthetic lethal target in SMARCA4-deficient cancer cells, and SMD-3236 has a 2000-fold selectivity for degradation of SMARCA2 over SMARCA4, with a DC50< 1 nM and a Dmax>95%. SMD-3236 can induce SMARCA2 loss in tumor tissues while retaining SMARCA4 protein, and inhibit tumor growth in the H838 smarca4-deficient human cancer xenograft model. SMD-3236 is composed of target protein ligand (red part) SMI-1074 (HY-170817), PROTAC linker (black part) (trans-4-Ethynylcyclohexyl)methyl methanesulfonate (HY-170825), and E3 ligase ligand (blue part) SMARCA2 ligand-14 (HY-170826), of which the E3 ligase ligand and linker form a conjugate E3 Ligase Ligand-linker Conjugate 159 (HY-170827)[1].

IC50 & Target

SMARC2, VHL-1[1]

分子量

1095.83

Formula

C61H75ClN10O5S

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

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

纯度 & 产品资料
参考文献
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产品名称:
SMD-3236
目录号:
HY-170824
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