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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
20653Contezolid free base1112968-42-998% Min.
Contezolid (Youxitai ®), an orally administered oxazolidinone antibacterial agent, i
20645CP-506 ( Synonyms: SN-36506 )2227304-19-898% Min.
CP-506 (SN-36506) is an hypoxia-activated prodrug of a DNA-alkylating nitrogen mustar
20632Censavudine634907-30-598% Min.
Censavudine, also known as OBP-601, BMS-986001 or festinavir, is a nucleoside reverse
20626CFI-402257 free base1610759-22-298% Min.
CFI-402257 was discontinued for commercial reason.
20622Cantharidine56-25-798% Min.
Cantharidine (free base) is a PP1/2A inhibitor found in Canarthis vesicatoria. It inh
20575Compound E209986-17-498% Min.
Compound E is a cell-permeable, potent, selective inhibitor of ɣ-secretase and Notch
205620990CL511514-03-798% Min.
0990CL is an inhibitor of heterotrimeric Gαi subunits. 0990CL showed direct interact
20558CBiPES HCl856702-40-498% Min.
CBiPES HCl is a selective positive allosteric modulator of the mGlu2 receptor.
20555COH1 inhibitor20217-22-598% Min.
COH1 is a ribonucleotide reductase (RR) inhibitor.
20510CC-92480 ( Mezigdomide )2259648-80-9≧98.0%
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno
20488CYM-503081345858-76-598% Min.
CYM 50308 is a novel agonist of SIP4 (EC50 = 56 nM) that displays 37-fold selectivity
20478CRANAD-281623747-97-698% Min.
CRANAD-28 is a blood brain barrier (BBB) penetrable two-photon imaging probe. It acts
20467CPPHA693288-97-098% Min.
CPPHA is a positive allosteric modulator of metabotropic glutamate receptor 5 (mGluR5
20455Camlipixant ( BLU-5937 )1621164-74-6≧98.0%
Camlipixant is an investigational, twice-daily oral P2X3 receptor antagonist for the
20441CMP3a647834-15-998% Min.
CMP3a is a NEK2 kinase inhibitor. CMP3a efficiently attenuated GBM growth in a mouse
122622CNS004695205-24-4≧98.0%
CNS004 is a novel compound that potentiates NMDA receptor currents based on glutamate
204236-Chloro-4-hydroxy-[1,5]naphthyridine-3-carboxylic acid ethyl ester127094-58-098% Min.
204186-chloro-4-(ethylamino)-3-Pyridinecarboxaldehyde959163-01-098% Min.
204083-(chloromethyl)-2-(1-isopropyl-1H-pyrazol-5-yl)pyridine hydrochloride1446321-95-498% Min.
203932-(4-chlorophenyl)-2,2-difluoroacetic acid475301-73-698% Min.
203872-Chloro-4'-fluoroacetophenone456-04-298% Min.
G203854-cyclohexyl-1,1-dimethylpiperazin-1-ium iodide865144-54-398% Min.
822225Cadisegliatin (TTP-399)859525-02-3≧98.0%
Cadisegliatin(TTP-399) is a potential liver-selective glucokinase (GK) activator for
L20350CR8 hydrochloride1786438-30-998% Min.
CR8 is a potent and selective inhibitor of CDK. CR8 is a more potent pyridyl analogue
L20348CCT020312324759-76-498% Min.
CCT020312 is a potent and selective EIF2AK3 Activator. CCT020312 modulates the biolog
L20343CC-6711618658-88-098% Min.
CC-671 is a potent and selective dual inhibitor of TTK (Mps1) and CLK2.
L20340CS-26671258296-60-498% Min.
RO495 (CS-2667) is a potent inhibitor of Non-receptor tyrosine-protein kinase 2 (TYK2
203283-cyclopropyl-7-methyl-6-nitro-2H-benzo[e][1,3]oxazin-4(3H)-one1038984-34-796% Min.
20322CB-103218457-67-198% Min.
CB-103 is a γ-secretase inhibitor. CB-103 inhibits Notch signaling in primary human
20313Cenerimod ( ACT-334441 )1262414-04-9≧98.0%
Cenerimod is a potent and orally active immunomodulator, exhibited EC50 value of 2.7