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产品目录

编号化学名称Cas号纯度化学结构
2071538CM-2721846570-31-798% Min.
CM-272 is a first-in-class reversible dual small molecule inhibitor against G9a and D
20623172-Cyano-4-fluorobenzaldehyde77532-90-298% Min.
20623063-chloro-1-benzothiophene-2-carbonyl chloride21815-91-898% Min.
20620265-chloro-2,6-dimethoxy-4-methyl-8-nitroquinoline189746-21-296% Min.
20620224-(3-Chloro-2-fluoroanilino)-6-hydroxy-7-methoxyquinazoline612501-52-796% Min.
20620142-chloro-6-methoxy-4-methylquinoline6340-55-296% Min.
2061702CaCCinh-A01407587-33-198% Min.
CaCCinh-A01, also known as TMEM16 Blocker I, is a TMEM16 Blocker. CaCCinh-A01 is a no
615201CLEFMA1246964-32-898% Min.
CLEFMA has anti-proliferative activity in H441 cells. CLEFMA may induce autophagic ce
2061307 CMPD141179-33-398% Min.
CMPD1 is an inhibitor of MK2 activation, primarily inhibiting tubulin polymerisation
2061306CGP52411145915-58-898% Min.
CGP52411, also known as DAPH, is a selective inhibitor of the epidermal growth factor
2051505CADD522199735-88-198% Min.
CADD522 is a potent inhibitor of runt-related transcription factor-2 (RUNX2)-DNA bind
S-2041602-氯-7-氟喹啉-3-甲醛745830-16-498% Min.
S-203042铜色树碱524-63-098% Min.
2041501 CC-8851010100-07-898% Min.
CC-885 is a potent Cereblon Modulator with potent antitumor activity mediated through
203071CC-900091860875-51-998%
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
S510901Cenicriviroc Mesylate497223-28-698% Min.
Cenicriviroc(代号TAK-652,TBR-652)是用于治疗HIV感染的实验候选药物
193286CLP-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
193283CT-18121802632-22-9>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
193124Cevipabulin fumarate849550-67-0>98%
Cevipabulin fumarate (TTI-237 fumarate) 是一种口服活性微管活性抗肿瘤化
19342Conteltinib 1384860-29-0>98%
Conteltinib是一种酪氨酸激酶抑制剂和抗肿瘤药。
192274C25-140 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
192192CCT-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
191285CAY10602 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
19132Cilofexor ( 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
1812283CCT2417361402709-93-6>98%
CCT241736是一种有效且具有口服活性的日常FLT3-Aurora抑制剂。
1811292CA-4948 1801343-74-7>98%
CA-4948是一种生物活性化学物。
1810291CCT129202942947-93-5>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
1810232CBM 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