Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 24004 | T-1095 | 209746-59-8 | ≧96.0% |  |
| T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs). | ||||
| 24002 | Tert-butyl 6,11-dioxo-6,11-dihydro-5H-benzo[b]carbazole-2-carboxylate | 3024657-88-0 | ≧96.0% |  |
| Tert-butyl 6,11-dioxo-6,11-dihydro-5H-benzo[b]carbazole-2-carboxylate, CAS 3024657-88 | ||||
| 20660 | TT-012 | 1164471-33-3 | 98% Min. |  |
| TT-012 specifically binds to dynamic MITF and destroys the latter's dimer formati | ||||
| 20646 | TNG908 | 2760481-53-4 | ≧98.0% |  |
| TNG908 is a clinical stage MTA-cooperative PRMT5 inhibitor that is selectively active | ||||
| 20598 | Tilpisertib Fosmecarbil | 2567459-64-5 | 98% Min. |  |
| Tilpisertib fosmecarbil is a potent serine/threonine kinase inhibitor. | ||||
| 20565 | 1,1,1-Trifluoroethyl-PEG3-Propargyl | 1835759-73-3 | 98% Min. |  |
| 1,1,1-Trifluoroethyl-PEG3-Propargyl is a heterobifunctional reagent with an alkyne gr | ||||
| 20557 | TZ3O | 2218754-19-7 | 98% Min. |  |
| TZ3O (compound TZ30) is an anticholinergic agent with neuroprotective effects. | ||||
| 20553 | Tinengotinib ( TT-00420) | 2230490-29-4 | ≧98.0% |  |
| Tinengotinib ( TT-00420) is a novel multiple kinase inhibitor that strongly inhibited | ||||
| 236271 | TP1287 | 2044686-42-0 | ≧97.0% |  |
| Alvocidib Prodrug TP-1287 is an orally bioavailable, highly soluble phosphate prodrug | ||||
| 20474 | Tinlarebant | 1821327-95-0 | 98% Min. |  |
| 20465 | trans-ISRIB | 1597403-47-8 | 98% Min. |  |
| trans-ISRIB is an Integrated Stress Response Inhibitor. trans-ISRIB inhibits the eIF2 | ||||
| 20417 | Thiourea, N-(1S,2S,4R)-bicyclo[2.2.1]hept-2-yl- | 870708-65-9 | 98% Min. | -bicyclo[2.2.1]hept-2-yl-_870708-65-9.png) |
| 20409 | 2-(tert-butyldimethylsilyloxy)-N-methoxy-N-methylacetamide | 163089-34-7 | 98% Min. | -N-methoxy-N-methylacetamide_163089-34-7.png) |
| 20392 | 5-TERT-BUTYL-2-(CHLOROMETHYL)OXAZOLE | 224441-73-0 | 98% Min. | OXAZOLE_224441-73-0.png) |
| 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% | -2-FUROIC_ACID_54857-86-2.png) |
| 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. | QUINAZOLIN-4(3H)-ONE_16544-67-5.png) |
| 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% | _2062661-53-2.gif) |
| 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. | -1-(TRIISOPROPYLSILYL)-1H-INDOLE_690632-17-8.png) |
| 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. | .png) |
| TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A | ||||
| 2071631 | Triazavirin ( Riamilovir ) | 928659-17-0 | 98% | _928659-17-0.png) |
| 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. |  |