Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 17030204 | TWS-119 | 601514-19-6 | 98% |  |
| TWS-119 is a potent and selective inhibitor of glycogen synthase kinase-3 (IC50 = 30 | ||||
| 17030113 | Tenapanor HCl | 1234365-97-9 | 98% |  |
| Tenapanor, also known as AZD-1722 and RDX 5791, is an inhibitor of the sodium-proton | ||||
| 17030103 | Tirofiban HCl hydrate | 150915-40-5 | 98% |  |
| Tirofiban is an antiplatelet drug. It belongs to a class of antiplatelet named glycop | ||||
| 17022810 | TAS-109 | 135598-68-4 | 98% |  |
| TAS-109, also known as DFP-10917 and CNDAC, is an analogue of the nucleoside deoxycyt | ||||
| 17022401 | TRX818 | 1256037-58-7 | 98% | |
| TRX-818 is an orally bioavailable agent with potential antineoplastic and anti-vascul | ||||
| 17021310 | Trapidil | 15421-84-8 | 98% |  |
| Trapidil is a PDGF antagonist that can inhibit the proliferation of the PDGF-producin | ||||
| 17012103 | Tirabrutinib HCl | 1439901-97-9 | ≧98.0% |  |
| ONO-4059 is a selective and novel inhibitor of BTK with IC50 2.2 nm, ONO-4059 binds t | ||||
| 17011905 | Temozolomide Acid | 113942-30-6 | 98% |  |
| Temozolomide Acid, also known as TMZA, is a metabolite of temozolomide (TMZ) with dem | ||||
| 17011904 | Tildipirosin | 328898-40-4 | 98% |  |
| Tildipirosin (TIP) is a novel 16-membered-ring macrolide authorized for the treatment | ||||
| 17011728 | TH588 | 1609960-31-7 | 98% |  |
| TH588 is a potent inhibitor of human 7,8-Dihydro-8-oxoguaninetriphosphatase MTH1 (NUD | ||||
| 17011727 | TG6-10-1 | 1415716-58-3 | 98% |  |
| TG6-10-1 is a potent and selective antagonist for the prostaglandin E2 receptor subty | ||||
| 17011726 | TG101209 | 936091-14-4 | 98% |  |
| TG101209 is a novel and potent JAK2 inhibitor, which induced dose- and time-dependent | ||||
| 17011723 | Teniposide | 29767-20-2 | 98% |  |
| Teniposide is a semisynthetic derivative of podophyllotoxin with antineoplastic activ | ||||
| 17011722 | Telotristat ethyl | 1033805-22-9 | 98% |  |
| Telotristat ethyl, also known as LX 1032 or LX 1606, is an oral serotonin synthesis i | ||||
| 17011721 | Tebipenem pivoxil | 161715-24-8 | 98% |  |
| Tebipenem pivoxil, also known as ME1211 and TBM-PI, is a novel oral carbapenem antibi | ||||
| 17011720 | TC-H 106 | 937039-45-7 | 98% |  |
| TC-H 106, also known as Pimelic Diphenylamide 106, is a class I HDAC inhibitor, demon | ||||
| 17011719 | TAS-301 | 193620-69-8 | 98% |  |
| TAS-301 is a potent and selective constrictive remodeling regulator on renarrowing af | ||||
| 17011718 | TAS-103 | 174634-08-3 | 98% |  |
| TAS-103, also known as BMS-247615, is a quinoline derivative that displays antitumor | ||||
| 17011717 | Talabostat mesylate | 150080-09-4 | 98% |  |
| Talabostat, also known as PT-100, is dipeptidyl peptidase inhibitor with antineoplast | ||||
| 17011716 | TAK-659 HCl | 1312691-41-0 | 98% |  |
| TAK-659 is an inhibitor of spleen tyrosine kinase (syk), with potential anti-inflamma | ||||
| 17011715 | TAK-285 | 871026-44-7 | 98% |  |
| TAK-285 is a novel dual erbB protein kinase inhibitor that specifically targets human | ||||
| 17109008 | Tamsulosin hydrochloride | 106463-17-6 | 98% |  |
| Tamsulosin is a potent and selective α1a adrenergic receptor antagonist. Tamsulosin | ||||
| 16122840 | T-0901317 | 293754-55-9 | 98% |  |
| T-0901317, also known as T-1317; TO-091317; TO 901317, is a liver X receptor (LXR) ag | ||||
| 16122728 | Terazosin | 63074-08-8 | 98% |  |
| Terazosin is a selective alpha-1 antagonist used for treatment of symptoms of an enla | ||||
| 16122718 | Tubercidin | 69-33-0 | 98% |  |
| Tubercidin, an adenosine analogue, is a nucleoside antibiotic. It is incorporated int | ||||
| 6111515 | TPO agonist 1 | 1033040-23-1 | 98% |  |
| TPO agonist 1 can increase production of platelets by stimulating the TPO receptor in | ||||
| 61118 | TY-52156 | 934369-14-9 | 98% | |
| TY-52156 is a potent S1P3 receptor antagonist in a competitive manner, and the Ki val | ||||
| 61117 | TCS-OX2-29 | 372523-75-6 | 98% |  |
| TCS-OX2-29 is a potent and selective OX2 receptor antagonist with IC50 of 40 nM. Disp | ||||
| 6111013 | THZ1 | 1604810-83-4 | 98% | |
| THZ1 is a novel selective and potent covalent CDK7 inhibitor with IC50(binding affini | ||||
| 611934 | TZ9 | 1002789-86-7 | 98% | |
| TZ9 is a novel inhibitor of Rad6 ubiquitin conjugating enzyme(E2 enzyme); inhibits MD | ||||