Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
G20380 | TA-02 | 1784751-19-4 | 98% Min. | ![]() |
TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM. | ||||
20376 | TOFA ( RMI14514; MDL14514) | 54857-86-2 | ≧98.0% | ![]() |
TOFA ( RMI14514; MDL14514) is an allosteric inhibitor of acetyl-CoA carboxylase-α (A | ||||
G20373 | 1,7,9-Triazaspiro[4.5]dec-1-ene-6,10-dione, 2,4-bis(4-chlorophenyl)-8-thioxo- | 2377858-38-1 | 98% Min. | ![]() |
20311 | 6-(TRIFLUOROMETHYL)QUINAZOLIN-4(3H)-ONE | 16544-67-5 | 98% Min. | ![]() |
20279 | Teclozan | 5560-78-1 | 98% Min. | ![]() |
Teclozan is an antiprotozoal agent. It is a dichloroacetamide. | ||||
218701 | TOVINONTRINE ( IMR-687 ) | 2062661-53-2 | ≧98.0% | ![]() |
TOVINONTRINE ( IMR-687 ) is a highly selective and potent small molecule inhibitor of | ||||
21254 | 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1-(TRIISOPROPYLSILYL)-1H-INDOLE | 690632-17-8 | 98% Min. | ![]() |
21239 | Targocil | 1200443-21-5 | 98% Min. | ![]() |
Targocil is a antibiotic, inhibiting a late step in wall teichoic acid biosynthesis a | ||||
2121222 | Tasisulam | 519055-62-0 | 98% Min. | ![]() |
Tasisulam, also known as LY573636, is an acyl-sulfonamide with potential antineoplast | ||||
2112801 | trans-ISRIB | 1597403-47-8 | 98% Min. | ![]() |
trans-ISRIB is an Integrated Stress Response Inhibitor. trans-ISRIB inhibits the eIF2 | ||||
20736 | Tolebrutinib | 1971920-73-6 | 98% Min. | |
Tolebrutinib, also known as SAR442168, is a Bruton tyrosine kinase inhibitor. | ||||
2091903 | THAL-SNS-032 | 2139287-33-3 | 98% Min. | ![]() |
THAL-SNS-032 is a selective CDK9 degrader. THAL-SNS-032 consists of a CDK-binding SNS | ||||
2073107 | Trilaciclib hydrochloride (G1T28 hydrochloride) | 1977495-97-8 | 98% Min. | ![]() |
TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A | ||||
2071631 | Triazavirin ( Riamilovir ) | 928659-17-0 | 98% | ![]() |
Triazavirin (TZV, Riamilovir) is a broad-spectrum antiviral drug that is a nucleoside | ||||
2071541 | T-3775440 HCl | 1422535-52-1 | 98% Min. | ![]() |
T-3775440 HCl is a potent, selecitve, irreversible LSD1 inhibitor. | ||||
262322 | 2-(tert-butoxycarbonylamino)pyrazolo[1,5-a]pyridine-3-carboxylic acid | 1476799-74-2 | 98% Min. | ![]() |
2062321 | tert-Butyl 2-((tosyloxy)methyl)morpholine-4-carboxylate | 130546-33-7 | 98% Min. | |
2062318 | tert-butyl 3-bromo-5-chloro-2-fluorophenyl-carbamate | 1269232-94-1 | 98% Min. | |
2062310 | tert-butyl N-(4-bromo-2-methoxyphenyl)carbamate | 262433-01-2 | 98% Min. | |
2062302 | Thiazole-5-carboxylic acid | 14527-41-4 | 98% Min. | |
2062301 | tert-butyl N-[[4-[(Z)-C-chloro-N-hydroxycarbonimidoyl]phenyl]methyl]-N-methylcarbamate | 1402390-77-5 | 96% Min. | ![]() |
2062035 | tert-butyl 4-[[6-[2-(quinoxaline-2-carbonylamino)phenyl]imidazo[2,1-b][1,3]thiazol-3-yl]methyl]piperazine-1-carboxylate | 925436-46-0 | 96% Min. | ![]() |
2062034 | tert-Butyl 4-(1-oxoisoindolin-2-yl-methyl)piperidine-1-carboxylate | 359629-19-9 | 98% Min. | ![]() |
2062024 | 4,4,5,5-tetramethyl-2-(4-propan-2-ylsulfonylphenyl)-1,3,2-dioxaborolane | 1256359-13-3 | 96% Min. | ![]() |
2061704 | Tafenoquine-d3 succinate | 1133378-83-2 | 98% Min. | ![]() |
Tafenoquine-d3 is a trideuerium-labeled Tafenoquine derivative. Tafenoquine, also kno | ||||
2061501 | TLR4-C34 | 40592-88-9 | 98% Min. | ![]() |
TLR4-C34 is a TLR4 inhibitor that inhibits TLR4 signaling in enterocytes and macropha | ||||
2061311 | TH257 | 2244678-29-1 | 98% Min. | ![]() |
TH257 is a Potent and selective allosteric LIMK 1/2 inhibitor. | ||||
2061303 | TH-263 | 313520-94-4 | 98% Min. | ![]() |
TH-263 is an inactive analog control for the type III allosteric LIM-kinase (LIMK) in | ||||
S-204158 | 2,4,6-tris(4-phenylphenyl)-1,3,5-triazine | 31274-51-8 | 98% Min. | ![]() |
S-203041 | [4-(2,2,2-trifluoroethoxy)phenyl]boronic acid | 886536-37-4 | 95% | ![]() |
g scale to Kg scale may be provided. |
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