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| 目录号 | 产品名称 | 产品描述 |
| R2101003 | Nicardipine (YC-93 hydrochloride) | Nicardipine hydrochloride (YC-93) 是一种钙通道 (calcium channel) 阻滞剂，可阻断心脏钙通道，IC50 为 1 |
| R2101004 | 24-Norursodeoxycholic acid | 24-norursodeoxycholic acid (norUDCA) 是侧链缩短的 UDCA 的 C23 同系物，具有有效的抗胆汁淤积，抗炎和抗纤维化特性。 |
| R2101005 | MALAT1-IN-1 (compounds 5) | MALAT1-IN-1 (化合物5) 是一种有效且特异性的 Malat1 (转移相关的肺腺癌转录本 1) 抑制剂。MALAT1-IN-1 以剂量依赖性方式调节 |
| R2101006 | CRANAD-2 | CRANAD-2 is a curcumin-derivatized near-infrared (NIR) probe that meets all the |
| R2101007 | LDN-192960 hydrochlorid | LDN-192960 hydrochloride 是 Haspin 和 DYRK2 的双重抑制剂，IC50 值分别为 10 nM 和 48 nM。 |
| R2101008 | PF9601N | PF9601N is a selective and potent monoamine oxidase B inhibitor that exhibit ant |
| R2101009 | A286982 | A286982 is an inhibitor that blocks the integrin-ligand interaction between leuk |
| R2101010 | ML-180 | ML-180 (SR1848) 是一种有效的 orphan nuclear receptor NR5A2 (Liver receptor homologue-1 |
| R2101011 | ML095 (MLS-0315848;CID-25067483) hydrochloride | ML095 (MLS-0315848, CID-25067483) hydrochloride is a specific inhibitor of place |
| R2101012 | Dafadine-A | Dafadine-A是dafadine类似物，是C. elegans DAF-9 细胞色素P450抑制剂，还能抑制哺乳动物的CYP27A1。 |
| R2101013 | Fluxapyroxad | Fluxapyroxad is a broad-spectrum fungicide that inhibits the succinate dehydroge |
| R2101014 | WIKI4 | WIKI4是Wnt/_beta_-catenin信号转到抑制剂，EC50值约75nM。 |
| R2101015 | PCNA-I 1 | PCNA-I1 is a proliferating cell nuclear antigen (PCNA) inhibitor. It inhibits gr |
| R2101016 | CYM50308 | CYM50308 是一种有效的，选择性和高亲和力的鞘氨醇-1-磷酸受体 4 (S1P4-R) 激动剂，EC50 为 56 nM。CYM50308 对 S1P4- |
| R2101017 | BC-1215 | BC-1215 是 F-box protein 3 (FBXO3) 的抑制剂，IL-1β 释放时，IC50 值为 0.9 μg/mL。 BC-1215 降低 F |
| R2101018 | BC-1258 | 密度 1.2±0.1 g/cm3 沸点 599.9±60.0 °C at 760 mmHg 闪点 316.6±32.9 °C 蒸汽压 0.0±1.7 mmHg |
| R2101019 | BMS-191011 | BMS-191011 (BMS-A) 是一种大电导钙激活钾通道 (large-conductance, Ca2++-activated potassium (m |
| R2101020 | CRT0066101 dihydrochloride | CRT0066101 is a specific inhibitor of all Protein kinase D (PKD) isoforms. |
| R2101021 | AA92593 | AA92593 (Opn4 Antagonist) is a potent antagonist of melanopsin-mediated phototra |
| R2101022 | ML335 | ML335 (CYM 51010, CID-23723457) is an agonist for OPRM1(μ-opioid receptor)-OPRD1 |
| R2101023 | VK-II-36 | VK-II-36 is a carvedilol analog that suppresses sarcoplasmic reticulum (SR) Ca(2 |
| R2101024 | YMU1 | ML335 (CYM 51010, CID-23723457) is an agonist for OPRM1(μ-opioid receptor)-OPRD1 |
| R2101025 | ML254 | ML254 is shown to competitively interact with the MPEP allosteric binding site. |
| R2101026 | PU-H54 | A potent, selective Grp94 inhibitor. |
| R2101027 | ML303 | ML303 是一种吡唑并吡啶类化合物， 是流感病毒非结构蛋白 1 (NS1) 的拮抗剂 (IC90 为 155 nM)，其对流感病毒H1N1亚型的 EC50 值 |
