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| 目录号 | 产品名称 | 产品描述 |
| 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 |
| R2101112 | BGC-20-1531 | BGC-20-1531 is a EP4 antagonist for the treatment of acute migraine. |
| R2101113 | Aka Lumine | AkaLumine is a luciferin analogue. The bioluminescence produced by AkaLumine in |
| R2101114 | SGC2085 hydrochloride | SGC2085 is a potent and selective coactivator associated arginine methyltransfer |
| R2101115 | TMP778 | TMP778 是一种有效的、RORγt 的选择性反向激动剂，其 FRET 检测出的 IC50 值为 7 nM。 |
| R2101116 | TX1-85-1 | TX1-85-1 是一种 Her3 (ErbB3) 抑制剂，IC50 值为 23 nM。TX1-85-1 可诱发 Her3 蛋白的部分降解并减弱 Her3 依赖 |
| R2101117 | Azaindole 1;TC-S 7001 | Azaindole 1 是一种高效的人 ROCK-1 和 ROCK-2 抑制剂，IC50 值分别为 0.6 和 1.1 nM，同时可抑制小鼠和大鼠 ROCK-2 |
| R2101118 | Shield-1 | Shield-1 是特异性，细胞可渗透的，高亲和力 FK506 结合蛋白-12 (FKBP) 配体，通过与突变的 FKBP (mtFKBP) 结合而逆转其不稳定 |
| R2101119 | NCGC00262650 | NCGC00262650 is a dual inhibitor of AMA1-RON2 interaction and c-Src tyrosine kin |
| R2101120 | ERDRP-0519 | ERDRP-0519 is an orally available polymerase inhibitor. It shows efficacy agains |
| R2101121 | AQX-016A | AQX-016A is a potent activator of SHIP-1 that induces apoptosis of the cancer ce |
| R2101122 | WWL229 | WWL229 is a selective Ces3 inhibitor. It acts by inhibiting recombinant Ces3 but |
| R2101123 | KLH45 | KLH45 is a selective inhibitor of DDHD2 (DDHD domain containing 2). |
| R2101124 | AA 41612 | AA 41612 is a potent, synthetic melanopsin antagonist with IC50 of 15.8 nM, atte |
| R2101125 | ML-349 | ML349 是一个有效且特异的酰基蛋白硫酯酶 2 (APT-2) 抑制剂，其 Ki 值为 120 nM。ML349 也是 LYPLA2 的抑制剂，其 IC50 |
| R2101126 | GNE-140 racemate | GNE-140外消旋体是一种新型高效乳酸脱氢酶（LDHA）抑制剂。在MIA-PaCa-2人胰腺细胞中，LDHA抑制迅速影响了整体代谢，但细胞死亡只发生在持续抑制 |
| R2101127 | Soporidine | Soporidine is a strigolactone (SL) antagonist and inhibitor of germination in th |
