Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
20653 | Contezolid free base | 1112968-42-9 | 98% Min. | |
Contezolid (Youxitai ®), an orally administered oxazolidinone antibacterial agent, i | ||||
20645 | CP-506 ( Synonyms: SN-36506 ) | 2227304-19-8 | 98% Min. | |
CP-506 (SN-36506) is an hypoxia-activated prodrug of a DNA-alkylating nitrogen mustar | ||||
20632 | Censavudine | 634907-30-5 | 98% Min. | |
Censavudine, also known as OBP-601, BMS-986001 or festinavir, is a nucleoside reverse | ||||
20626 | CFI-402257 free base | 1610759-22-2 | 98% Min. | |
CFI-402257 was discontinued for commercial reason. | ||||
20622 | Cantharidine | 56-25-7 | 98% Min. | |
Cantharidine (free base) is a PP1/2A inhibitor found in Canarthis vesicatoria. It inh | ||||
20575 | Compound E | 209986-17-4 | 98% Min. | |
Compound E is a cell-permeable, potent, selective inhibitor of ɣ-secretase and Notch | ||||
20562 | 0990CL | 511514-03-7 | 98% Min. | |
0990CL is an inhibitor of heterotrimeric Gαi subunits. 0990CL showed direct interact | ||||
20558 | CBiPES HCl | 856702-40-4 | 98% Min. | |
CBiPES HCl is a selective positive allosteric modulator of the mGlu2 receptor. | ||||
20555 | COH1 inhibitor | 20217-22-5 | 98% Min. | |
COH1 is a ribonucleotide reductase (RR) inhibitor. | ||||
20510 | CC-92480 ( Mezigdomide ) | 2259648-80-9 | ≧98.0% | |
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno | ||||
20488 | CYM-50308 | 1345858-76-5 | 98% Min. | |
CYM 50308 is a novel agonist of SIP4 (EC50 = 56 nM) that displays 37-fold selectivity | ||||
20478 | CRANAD-28 | 1623747-97-6 | 98% Min. | |
CRANAD-28 is a blood brain barrier (BBB) penetrable two-photon imaging probe. It acts | ||||
20467 | CPPHA | 693288-97-0 | 98% Min. | |
CPPHA is a positive allosteric modulator of metabotropic glutamate receptor 5 (mGluR5 | ||||
20455 | Camlipixant ( BLU-5937 ) | 1621164-74-6 | ≧98.0% | |
Camlipixant is an investigational, twice-daily oral P2X3 receptor antagonist for the | ||||
20441 | CMP3a | 647834-15-9 | 98% Min. | |
CMP3a is a NEK2 kinase inhibitor. CMP3a efficiently attenuated GBM growth in a mouse | ||||
122622 | CNS004 | 695205-24-4 | ≧98.0% | |
CNS004 is a novel compound that potentiates NMDA receptor currents based on glutamate | ||||
20423 | 6-Chloro-4-hydroxy-[1,5]naphthyridine-3-carboxylic acid ethyl ester | 127094-58-0 | 98% Min. | |
20418 | 6-chloro-4-(ethylamino)-3-Pyridinecarboxaldehyde | 959163-01-0 | 98% Min. | |
20408 | 3-(chloromethyl)-2-(1-isopropyl-1H-pyrazol-5-yl)pyridine hydrochloride | 1446321-95-4 | 98% Min. | |
20393 | 2-(4-chlorophenyl)-2,2-difluoroacetic acid | 475301-73-6 | 98% Min. | |
20387 | 2-Chloro-4'-fluoroacetophenone | 456-04-2 | 98% Min. | |
G20385 | 4-cyclohexyl-1,1-dimethylpiperazin-1-ium iodide | 865144-54-3 | 98% Min. | |
822225 | Cadisegliatin (TTP-399) | 859525-02-3 | ≧98.0% | |
Cadisegliatin(TTP-399) is a potential liver-selective glucokinase (GK) activator for | ||||
L20350 | CR8 hydrochloride | 1786438-30-9 | 98% Min. | |
CR8 is a potent and selective inhibitor of CDK. CR8 is a more potent pyridyl analogue | ||||
L20348 | CCT020312 | 324759-76-4 | 98% Min. | |
CCT020312 is a potent and selective EIF2AK3 Activator. CCT020312 modulates the biolog | ||||
L20343 | CC-671 | 1618658-88-0 | 98% Min. | |
CC-671 is a potent and selective dual inhibitor of TTK (Mps1) and CLK2. | ||||
L20340 | CS-2667 | 1258296-60-4 | 98% Min. | |
RO495 (CS-2667) is a potent inhibitor of Non-receptor tyrosine-protein kinase 2 (TYK2 | ||||
20328 | 3-cyclopropyl-7-methyl-6-nitro-2H-benzo[e][1,3]oxazin-4(3H)-one | 1038984-34-7 | 96% Min. | |
20322 | CB-103 | 218457-67-1 | 98% Min. | |
CB-103 is a γ-secretase inhibitor. CB-103 inhibits Notch signaling in primary human | ||||
20313 | Cenerimod ( ACT-334441 ) | 1262414-04-9 | ≧98.0% | |
Cenerimod is a potent and orally active immunomodulator, exhibited EC50 value of 2.7 |
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