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首页 > 产品展示
| 目录号 | 产品名称 | 产品描述 |
| R2101087 | CMPD101 | CMPD101，一种新型膜通透性 GRK2 和 GRK3 的小分子抑制剂，IC50 值分别为 18 nM 和 5.4 nM。CMPD101 还抑制 ROCK-2 |
| R2101088 | GSK121 trifluoroacetate | GSK121 is a selective inhibitor of PAD4. |
| R2101089 | GSK106 hydrochloride | GSK106 is a negative control compound that can be used in binding and functional |
| R2101090 | MSBN | MSBN是一种高选择性的硫醇荧光探针，选择性地成像活体细胞中的硫醇，并用一个启动信号特别标记蛋白质硫醇，以确定各种可逆的蛋白质硫醇修饰。 |
| R2101091 | ONO-8130 | ONO-8130 is an orally available EP1 receptor antagonist. |
| R2101092 | ML311 | ML311 是 Mcl-1/Bim 蛋白之间相互作用的有效选择性抑制剂。 |
| R2101093 | RO5203648 | A potent and selective TAAR1 partial agonist with Ki of 0.5, 1.0, 6.8 and 2.6 nM |
| R2101094 | PF-CBP1 | PF-CBP1是一种CREB结合蛋白溴区的高度选择性抑制剂。 |
| R2101095 | PF-CBP1 hydrochloride | PF-CBP1盐酸盐是一种CREB结合蛋白溴区的高度选择性抑制剂。 |
| R2101096 | TSPC | TSPC is an inhibitor for GA perception by in vitro and in planta evaluations. |
| R2101097 | SHA68 | SHA 68 是一种有效的选择性非肽神经肽 S 受体 (NPSR) 拮抗剂，对 NPSR Asn107 和 NPSR Ile107 的 IC50 分别为 22. |
| R2101098 | GSK963 | GSK963 是一种手性的、强效的、选择性的受体相互作用蛋白 1 (RIP1) 酶的抑制剂，其 IC50 值为 29 nM。GSK963 对体外小鼠和人细胞的坏 |
| R2101099 | GSK962 | GSK962 是 GSK963 的非活性对映异构体，可用于确认靶点作用。 |
| R2101100 | NSC45586 | A selective protein phosphatase PHLPP inhibitor with IC50 of 4 uM for PP2C domai |
| R2101101 | ML198 | ML198 is a novel activator and non-inhibitory chaperone of glucocerebrosidase. M |
| R2101102 | Ribocil | Ribocil是一种高度选择性的化学调节剂, 调节细菌核糖核黄素核开关, Ribocil强烈抑制GFP表达, EC50值为0.3 μM。 |
| R2101103 | Farampator (CX-691;Org24448) | Farampator (CX-691;Org24448) 是一种AMPA受体正调节剂。 |
| R2101104 | GSK3 Inhibitor XIII | GSK3 Inhibitor XIII (GSK3i XIII) is an ATP-binding site inhibitor of GSK-3. |
| R2101105 | pythiDC | PythiDC is a selective inhibitor of collagen prolyl 4-hydroxylase. |
| R2101106 | (S)SHA-68 | SHA-68 is a selective neuropeptide S receptor (NPSR) antagonist that displays no |
| R2101107 | NCGC607 | NCGC607 is a a small-molecule noninhibitory chaperone of glucocerebrosidase. |
| R2101108 | ML266 (CID-46943215) | ML266 (CID-46943215) is a activator of glucocerebrosidase (GCase) that does not |
| R2101109 | BMS986187 | BMS-986187 is a novel potent, positive allosteric modulator of δ-opioid receptor |
| R2101110 | BMS986188 | BMS-986188 is a positive allosteric modulator (PAM) of δ-opioid receptors with E |
| R2101111 | R243 | R243是一种有效的小分子CCR8拮抗剂，可抑制CCR8信号传导和趋化性，抑制CCL1诱导的Ca2+通量和CCL1驱动的腹膜巨噬细胞在0.2μM时聚集；减弱TN |
