编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
2071538 | CM-272 | 1846570-31-7 | 98% Min. | ![]() |
CM-272 is a first-in-class reversible dual small molecule inhibitor against G9a and D | ||||
2062317 | 2-Cyano-4-fluorobenzaldehyde | 77532-90-2 | 98% Min. | |
2062306 | 3-chloro-1-benzothiophene-2-carbonyl chloride | 21815-91-8 | 98% Min. | |
2062026 | 5-chloro-2,6-dimethoxy-4-methyl-8-nitroquinoline | 189746-21-2 | 96% Min. | ![]() |
2062022 | 4-(3-Chloro-2-fluoroanilino)-6-hydroxy-7-methoxyquinazoline | 612501-52-7 | 96% Min. | ![]() |
2062014 | 2-chloro-6-methoxy-4-methylquinoline | 6340-55-2 | 96% Min. | ![]() |
2061702 | CaCCinh-A01 | 407587-33-1 | 98% Min. | ![]() |
CaCCinh-A01, also known as TMEM16 Blocker I, is a TMEM16 Blocker. CaCCinh-A01 is a no | ||||
615201 | CLEFMA | 1246964-32-8 | 98% Min. | ![]() |
CLEFMA has anti-proliferative activity in H441 cells. CLEFMA may induce autophagic ce | ||||
2061307 | CMPD1 | 41179-33-3 | 98% Min. | ![]() |
CMPD1 is an inhibitor of MK2 activation, primarily inhibiting tubulin polymerisation | ||||
2061306 | CGP52411 | 145915-58-8 | 98% Min. | ![]() |
CGP52411, also known as DAPH, is a selective inhibitor of the epidermal growth factor | ||||
2051505 | CADD522 | 199735-88-1 | 98% Min. | ![]() |
CADD522 is a potent inhibitor of runt-related transcription factor-2 (RUNX2)-DNA bind | ||||
S-204160 | 2-氯-7-氟喹啉-3-甲醛 | 745830-16-4 | 98% Min. | ![]() |
S-203042 | 铜色树碱 | 524-63-0 | 98% Min. | ![]() |
2041501 | CC-885 | 1010100-07-8 | 98% Min. | ![]() |
CC-885 is a potent Cereblon Modulator with potent antitumor activity mediated through | ||||
203071 | CC-90009 | 1860875-51-9 | 98% | ![]() |
CC-90009 是一种 cereblon (CRBN) E3 连接酶调节剂。CC-90009 与 CRBN 特异性 | ||||
4281903 | 5-氯-2,6-二甲氧基-4-甲基喹啉 | 189746-19-8 | >96% | ![]() |
5-氯-2,6-二甲氧基-4-甲基喹啉是一个他非诺喹原料药合成中非常关 | ||||
S510901 | Cenicriviroc Mesylate | 497223-28-6 | 98% Min. | ![]() |
Cenicriviroc(代号TAK-652,TBR-652)是用于治疗HIV感染的实验候选药物 | ||||
193286 | CLP-290 | 1181083-81-7 | >98% | ![]() |
CLP-290是一种新型的KCC2调制器和CLP-257的前药,对KCC2相关的Cl-转运 | ||||
193283 | CT-1812 | 1802632-22-9 | >98% | ![]() |
CT-1812是一类口服的sigma-2/PGRMC1拮抗剂(α-β-低聚物受体拮抗剂),目 | ||||
193181 | 氯非铵甲苯磺酸盐 | 92953-10-1 | >98% | ![]() |
氯非铵甲苯磺酸盐是一种K+通道阻滞剂、心脏抑制剂和抗心律失常 | ||||
193124 | Cevipabulin fumarate | 849550-67-0 | >98% | ![]() |
Cevipabulin fumarate (TTI-237 fumarate) 是一种口服活性微管活性抗肿瘤化 | ||||
19342 | Conteltinib | 1384860-29-0 | >98% | ![]() |
Conteltinib是一种酪氨酸激酶抑制剂和抗肿瘤药。 | ||||
192274 | C25-140 | 1358099-18-9 | >98% | ![]() |
C25-140是环-E3连接酶(TRAF6) / E2酶(Ubc13)结合的一级蛋白-蛋白相互作用 | ||||
192192 | CCT-137690 | 1095382-05-0 | >98% | ![]() |
CCT137690是一种极光激酶抑制剂CCT137690,是一种高选择性的口服生物 | ||||
191285 | CAY10602 | 374922-43-7 | >98% | ![]() |
CAY10602是SIRT1激活剂。CAY10602是通过高通量筛选增加sirt1介导的特定 | ||||
19132 | Cilofexor ( GS-9674 ) | 1418274-28-8 | ≧98.0% | ![]() |
Cilofexor(也称为 GS-9674)是一种非甾体法尼醇 X 受体(FXR)激动剂 | ||||
1812283 | CCT241736 | 1402709-93-6 | >98% | ![]() |
CCT241736是一种有效且具有口服活性的日常FLT3-Aurora抑制剂。 | ||||
1811292 | CA-4948 | 1801343-74-7 | >98% | ![]() |
CA-4948是一种生物活性化学物。 | ||||
1810291 | CCT129202 | 942947-93-5 | >98% | ![]() |
CCT129202是Aurora激酶活性的抑制剂,在临床前研究中表现出良好的抗 | ||||
1810232 | CBM 301940 | 902146-11-6 | >98% | ![]() |
CBM 301940是一种有效的丙二酰辅酶a脱羧酶抑制剂,具有口服生物有 |