Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
203071 | CC-90009 | 1860875-51-9 | 98% | |
CC-90009 is a modulator of cereblon (CRBN), which is part of the cullin 4-RING E3 ubi | ||||
4281903 | 5-Chloro-2,6-Dimethoxy-4-Methylquinoline | 189746-19-8 | >96% | |
5-Chloro-2,6-Dimethoxy-4-Methylquinoline, CAS 189746-19-8, is a key drug intermediate | ||||
S510901 | Cenicriviroc Mesylate | 497223-28-6 | 98% Min. | |
Cenicriviroc (CVC) is an oral, once-daily, potent immunomodulator that blocks two che | ||||
193286 | CLP-290 | 1181083-81-7 | >98% | |
CLP-290 is a novel KCC2 modulator and prodrug of CLP-257, highly selective for KCC2 o | ||||
193283 | CT-1812 | 1802632-22-9 | >98% | |
CT-1812 is a first-in-class, orally available sigma-2/PGRMC1 antagonist (alpha beta o | ||||
193181 | Clofilium Tosylate | 92953-10-1 | >98% | |
Clofilium Tosylate is a K+ channel blocker, cardiac depressant, and anti-arrhythmic a | ||||
193124 | Cevipabulin fumarate | 849550-67-0 | >98% | |
Cevipabulin fumarate (TTI-237 fumarate) is an oral active, microtubule-active antitum | ||||
19342 | Conteltinib | 1384860-29-0 | >98% | |
Conteltinib is a tyrosine kinase inhibitor and an antineoplastic. | ||||
192274 | C25-140 | 1358099-18-9 | >98% | |
C25-140 is the first in class protein-protein interaction inhibitor of a RING-E3 liga | ||||
192192 | CCT-137690 | 1095382-05-0 | >98% | |
CCT137690, an aurora kinase inhibitor CCT137690, is a highly selective, orally bioava | ||||
191285 | CAY10602 | 374922-43-7 | >98% | |
CAY10602 is a SIRT1 activator. CAY10602 was derived from high throughput screening fo | ||||
19132 | Cilofexor ( GS-9674 ) | 1418274-28-8 | ≧98.0% | |
Cilofexor (also known as GS-9674) is a nonsteroidal farnesoid X receptor (FXR) agonis | ||||
1812283 | CCT241736 | 1402709-93-6 | >98% | |
CCT241736 is a potent and orally active and dual FLT3-Aurora inhibitor. | ||||
1811292 | CA-4948 | 1801343-74-7 | >98% | |
CA-4948 is a bioactive chemical. | ||||
1810291 | CCT129202 | 942947-93-5 | >98% | |
CCT129202 is an inhibitor of Aurora kinase activity and displays a favorable antineop | ||||
1810232 | CBM 301940 | 902146-11-6 | >98% | |
CBM 301940 is a potent malonyl-CoA decarboxylase inhibitor that is orally bioavailabl | ||||
1810225 | CID16020046 | 834903-43-4 | >98% | |
CID16020046 is a selective GPR55 inverse agonist. | ||||
1810161 | 10-Cl-BBQ | 23982-76-5 | >98% | |
10-Cl-BBQ is an aryl hydrocarbon receptor (AhR) ligand. | ||||
18792 | CGP-71683A HCl | 192322-50-2 | >98% | |
CGP 71683A is a potent and highly selective non-peptide antagonist of the NPY Y(5) re | ||||
18752 | Carumonam Sodium | 86832-68-0 | >98% | |
Carumonam Sodium, also known as Amasulin and AMA-1080, is a monobactam, penicillin bi | ||||
186281 | CEP-40783 | 1437321-24-8 | >98% | |
CEP-40783, also known as RXDX-106, is a potent, selective and orally available inhibi | ||||
185316 | CD437 | 125316-60-1 | >98% | |
CD437 is a synthetic retinoid that is an RARγ-selective agonist. | ||||
185315 | CB-1158 | 1345810-21-0 | >98% | |
CB-1158, also known as INCB01158, is a potent arginase inhibitor. | ||||
185291 | Cilomilast | 153259-65-5 | >98% | |
Cilomilast (Ariflo, SB-207,499) is a drug which was developed for the treatment of re | ||||
185174 | CNX-1351 | 1276105-89-5 | >98% | |
CNX-1351 is a selective covalent Inhibitor of PI3Kα. | ||||
185171 | CGP60474 | 164658-13-3 | >98% | |
CGP60474 is a potent dual cdk1/cdk2 inhibitor (IC50 values are 20 and 50 nM, respecti | ||||
184127 | COH29 | 1190932-38-7 | >98% | |
COH29 is an orally available, aromatically substituted thiazole and inhibitor of the | ||||
18491 | CIL56 | 300802-28-2 | >98% | |
CIL56 is a YAP1 inhibitor. It acts by inducing non-apoptotic cell death, triggering c | ||||
18444 | Casopitant mesylate | 414910-30-8 | >98% | |
Casopitant mesylate is the mesylate salt of a centrally-acting neurokinin 1 (NK1) rec | ||||
184320 | COTI-2 | 1039455-84-9 | >98% | |
COTI-2 is an P53 gene modulator and AKT2 inhibitor. OTI-2 is active against multiple |
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