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Cat. No.	Product Name	Field of Application
DC10281	Terconazole	Terconazole is a broad-spectrum antifungal medication for the treatment of vaginal yeast infection.
DC9155	Terfenadine	Terfenadine is a potent open-channel blocker of hERG with a mean IC50 of 204 nM.
DC4221	Teriflunomide(A-771726) Featured	Teriflunomide: Teriflunomide, aslo know as A77 1726 (trade name Aubagio, marketed by Sanofi) is the active metabolite of leflunomide.
DC21958	tert-butyl 2-cyano-5,8-dihydropyrido[3,4-d]pyrimidine-7(6H)-carboxylate	tert-butyl 2-cyano-5,8-dihydropyrido[3,4-d]pyrimidine-7(6H)-carboxylate..
DC22245	TES-1025 Featured	TES-1025 (TES1025) is a potent, selective inhibitor of human ACMSD (α-Amino-β-carboxymuconate-ε-semialdehyde decarboxylase) with IC50 of 13 nM, increases NAD+ levels in cellular systems.
DC12150	TES-991	TES-991 is a potent and selective human α‑Amino-β-carboxymuconate-ε-semialdehyde Decarboxylase (ACMSD) inhibitor, with an IC50 of 3 nM.
DC7316	Tesmilifene	Tesmilifene is a novel agent that augments cytotoxicity of various chemotherapeutic agents both in vitro and in vivo. It binds selectively to the high-affinity microsomal antiestrogen binding site (Ki=50nm) but has no affinity for estrogen receptors. Inhi
DC23675	Tetomilast	Tetomilast (OPC-6535) is a superoxide anion production inhibitor that inhibits PDE4 and proinflammatory functions of leukocytes including superoxide production and cytokine release.
DC9866	Tetrabenazine Featured	Tetrabenazine has been used for dopamine uptake assays in mouse brain cells1.
DC9041	Tetracaine HCl	Tetracaine HCl is a potent local anaesthetic and a channel function allosteric inhibitor.
DCAPI1291	Tetracycline HCl	Tetracycline HCl
DC12218	Tetradecanoylcarnitine Featured	Tetradecanoylcarnitine is a human carnitine involved in β-oxidation of long-chain fatty acids.
DCAPI1289	Tetrahydropapaverine HCl	Tetrahydropapaverine HCl
DC9374	6-TAMRA	Tetramethylrhodamine (TMR, TRITC) has been a widely used fluorophore for preparing bioconjugates, especially fluorescent antibody and avidin derivatives used in immunochemistry.
DC9361	Tetramisole (hydrochloride)	Tetramisole hydrochloride is an inhibitor of alkaline phosphatases, is a high purity antiparasitic.
DC23911	Tetrodotoxin citrate	Tetrodotoxin (TTx) is a potent, highly selective sodium channel blocker with IC50 of 33 nM for Nav1.6.
DC21252	Tezampanel	Tezampanel (LY 293558, NGX 424) is a competitive antagonist of the AMPA and kainate receptors with selectivity for the GluR5 subtype of the kainate receptor.
DC8932	TG003 Featured	TG003 is a potent and ATP-competitive Cdc2-like kinase (Clk) inhibitor with IC50 of 20 nM, 200 nM, and 15 nM for Clk1, Clk2, and Clk4, respectively. No inhibitory effect on Clk3, SRPK1, SRPK2, or PKC.
DC22308	TG4-155 Featured	TG4-155 is a brain penetrant EP2 antagonist (KB = 2.4 nM) that is over 1000-fold less effective at EP4 (KB = 11.4 µM) and a panel of other receptors and channels. It blocks the induced expression of inflammatory markers in microglial cells.
DC21748	TG693 Featured	TG693 is an orally available, selective, ATP-competitive CLK1 inhibitor with IC50 of 112.6 nM.
DC12506	TG8-69 Featured	TG8-69 is a peripherally restricted, highly potent, selective, aqueous-soluble EP2 antagonist with Kb of 48.5 nM.
DC7559	TGF-B (beta) receptor inhibitor Featured	TGF-β receptor inhibitor
DC12042	TGN-020 Featured	TGN 020 is a thiadiazole derivative studied for its potential antitumor properties
DC25110	TGR-1202 R-enantiomer	TGR-1202 R-enantiomer is is the less active enantiomer of TGR-1202 (Umbralisib), TGR-1202 is a potent, selective, orally available PI3Kδ inhibitor with IC50 of 22 nM..
DC21750	TH 5427	TH 5427 (TH5427) is a potent, small molecule NUDT5 (NUDIX5) inhibitor with IC50 of 29 nM, 690-fold selectivity for NUDT5 over MTH1 (NUDT1) in vitro.
DC12564	TH-257 Featured	TH-257 (TH257) is a potent, selective, allosteric inhibitor of LIMK1 and LIMK2 with IC50 of 84 nM for LIMK1 and 39 nM for LIMK2 in a RapidFire MS assay.
DC23145	TH5487 Featured	TH5487 (TH-5487, TH 5487) is a potent, selective, active-site inhibitor of 8-oxoguanine DNA glycosylase 1 (OGG1) with IC50 of 342 nM, prevents OGG1 from binding to its DNA substrate.
DC26123	Thalidomide-O-amido-C3-NH2	Thalidomide-O-amido-C3-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.
DC26125	Cereblon Ligand-Linker Conjugates 3 (TFA) Featured	Thalidomide-O-amido-PEG3-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology.
DC20289	(1S,2S)-2-PCCA	The (1R,2R) diastereomer of 2-PCCA, a potent, selective agonist of the orphan GPR88 receptor with EC50 of 373 nM, 5-fold more potent than the (1S, 2S)-isomer..

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