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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
G20380TA-021784751-19-498% Min.
TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM.
20376TOFA ( RMI14514; MDL14514)54857-86-2≧98.0%
TOFA ( RMI14514; MDL14514) is an allosteric inhibitor of acetyl-CoA carboxylase-α (A
G203731,7,9-Triazaspiro[4.5]dec-1-ene-6,10-dione, 2,4-bis(4-chlorophenyl)-8-thioxo-2377858-38-198% Min.
203116-(TRIFLUOROMETHYL)QUINAZOLIN-4(3H)-ONE16544-67-598% Min.
20279Teclozan5560-78-198% Min.
Teclozan is an antiprotozoal agent. It is a dichloroacetamide.
218701TOVINONTRINE ( IMR-687 )2062661-53-2≧98.0%
TOVINONTRINE ( IMR-687 ) is a highly selective and potent small molecule inhibitor of
212544-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1-(TRIISOPROPYLSILYL)-1H-INDOLE690632-17-898% Min.
21239Targocil1200443-21-598% Min.
Targocil is a antibiotic, inhibiting a late step in wall teichoic acid biosynthesis a
2121222Tasisulam519055-62-098% Min.
Tasisulam, also known as LY573636, is an acyl-sulfonamide with potential antineoplast
2112801trans-ISRIB1597403-47-898% Min.
trans-ISRIB is an Integrated Stress Response Inhibitor. trans-ISRIB inhibits the eIF2
20736Tolebrutinib1971920-73-698% Min.
Tolebrutinib, also known as SAR442168, is a Bruton tyrosine kinase inhibitor.
2091903THAL-SNS-0322139287-33-398% Min.
THAL-SNS-032 is a selective CDK9 degrader. THAL-SNS-032 consists of a CDK-binding SNS
2073107Trilaciclib hydrochloride (G1T28 hydrochloride)1977495-97-898% Min.
TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A
2071631Triazavirin ( Riamilovir )928659-17-098%
Triazavirin (TZV, Riamilovir) is a broad-spectrum antiviral drug that is a nucleoside
2071541T-3775440 HCl1422535-52-198% Min.
T-3775440 HCl is a potent, selecitve, irreversible LSD1 inhibitor.
2623222-(tert-butoxycarbonylamino)pyrazolo[1,5-a]pyridine-3-carboxylic acid1476799-74-298% Min.
2062321tert-Butyl 2-((tosyloxy)methyl)morpholine-4-carboxylate130546-33-798% Min.
2062318 tert-butyl 3-bromo-5-chloro-2-fluorophenyl-carbamate1269232-94-198% Min.
2062310tert-butyl N-(4-bromo-2-methoxyphenyl)carbamate262433-01-298% Min.
2062302Thiazole-5-carboxylic acid14527-41-498% Min.
2062301tert-butyl N-[[4-[(Z)-C-chloro-N-hydroxycarbonimidoyl]phenyl]methyl]-N-methylcarbamate1402390-77-596% Min.
2062035tert-butyl 4-[[6-[2-(quinoxaline-2-carbonylamino)phenyl]imidazo[2,1-b][1,3]thiazol-3-yl]methyl]piperazine-1-carboxylate925436-46-096% Min.
2062034tert-Butyl 4-(1-oxoisoindolin-2-yl-methyl)piperidine-1-carboxylate359629-19-998% Min.
20620244,4,5,5-tetramethyl-2-(4-propan-2-ylsulfonylphenyl)-1,3,2-dioxaborolane1256359-13-396% Min.
2061704Tafenoquine-d3 succinate1133378-83-298% Min.
Tafenoquine-d3 is a trideuerium-labeled Tafenoquine derivative. Tafenoquine, also kno
2061501TLR4-C3440592-88-998% Min.
TLR4-C34 is a TLR4 inhibitor that inhibits TLR4 signaling in enterocytes and macropha
2061311TH2572244678-29-198% Min.
TH257 is a Potent and selective allosteric LIMK 1/2 inhibitor.
2061303TH-263313520-94-498% Min.
TH-263 is an inactive analog control for the type III allosteric LIM-kinase (LIMK) in
S-2041582,4,6-tris(4-phenylphenyl)-1,3,5-triazine31274-51-898% Min.
S-203041[4-(2,2,2-trifluoroethoxy)phenyl]boronic acid886536-37-495%
g scale to Kg scale may be provided.