DC10118 |
TD-198946
Featured
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TD-198946(TD198946 ) is a small molecule stimulator of chondrogenesis; promotes chondrocyte differentiation. |
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DC21745 |
TD-6450 |
TD-6450 is a next generation, potent HCV NS5A inhibitor that has potent antiviral activity against HCV infection.. |
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DC23751 |
TDI-2760 |
TDI-2760 si a small molecule Aβ-aggregation inhibitor that not only shows a strong inhibitory efficacy toward the Aβ-fibrinogen interaction (IC50=1.67 uM) but also retains potency toward the Aβ42 aggregation inhibition process. |
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DCAPI1082 |
Tebipenem pivoxil(L-084) |
Tebipenem pivoxil(L-084) |
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DC21552 |
Tecalcet |
Tecalcet (R-568. |
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DC21553 |
Tecalcet hydrochloride |
Tecalcet (R-568. |
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DC11026 |
Tecovirimat
Featured
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Tecovirimat (ST-246, Tpoxx) is a potent, orally bioavailable, first-in-class inhibitor of orthopoxvirus egress with EC50 of 0.01-0.6 uM against a panel of Orthopoxviruses; ST-246 is active against multiple orthopoxviruses, including vaccinia, monkeypox, c |
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DC12603 |
TED-347
Featured
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TED-347 (TED347) is an irreversible inhibitor of TEAD4-Yap1 protein-protein interaction (EC50=5.9 uM in FP asssays) via covalent modification of conserved cysteine (Cys367, Ki=1.3 uM), inhibits its binding to Yap1, blocked its transcriptional activity. |
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DC9352 |
(S)-Tedizolid |
Tedizolid is the active moiety of the prodrug tedizolid phosphate, with high potency against Gram-positive species.
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DC20756 |
Tegatrabetan
Featured
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Tegatrabetan (BC-2059, BC2059, Tegavivint) is an orally bioavailable β-catenin antagonist that disrupts the binding of β-catenin to TBL1 and promotes β-catenin degradation, attenuates nuclear and cytoplasmic levels of β-catenin. |
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DC7515 |
Teglicar
Featured
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Teglicar, in vitro and in animal models, reduces gluconeogenesis and improves glucose homeostasis, refreshing the interest in selective and reversible L-CPT1 inhibition as a potential antihyperglycemic approach. |
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DC20155 |
Tegoprazan
Featured
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Tegoprazan, a potassium-competitive acid blocker, is a potent, oral active and highly selective inhibitor of gastric H+/K+-ATPase that could control gastric acid secretion and motility, with IC50 values ranging from 0.29-0.52 μM for porcine, canine, and human H+/K+-ATPases in vitro. |
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DCAPI1555 |
Teicoplanin
Featured
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Teicoplanin Complex is a complex of antibiotics produced by Actinoplanes teichomyceticus. Teicoplanin, the major component of Teicoplanin Complex, is a glycopeptide antibiotic structurally similar to Vancomycin (sc-204938) and Ristocetin (sc-202318). As a |
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DC4211 |
Telbivudine |
Telbivudine (Tyzeka, Sebivo) is an antiviral agent used in the treatment of hepatitis B infection. |
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DCAPI1102 |
Telithromycin (Ketek)
Featured
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Telithromycin (Ketek) |
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DCAPI1465 |
Telmisartan |
Telmisartan is an angiotensin II receptor antagonist that inhibits the angiotensin II AT1 receptor. |
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DC23164 |
Telotristat |
Telotristat (LP-778902) is a potent, small-molecule inhibitor of peripheral serotonin synthesis, acts by inhibiting tryptophan hydroxylase (TPH) with IC50 of 28 nM, demonstrates potential for the treatment of carcinoid syndrome.. |
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DCAPI1118 |
Tempol (4-Hydroxy-TEMPO) |
TEMPOL (4-Hydroxy-TEMPO) is a superoxide scavenger that displays neuroprotective, anti-inflammatory and analgesic effects. |
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DC20721 |
Tenapanor hydrochloride |
Tenapanor (AZD-1722;RDX5791) is a potent, selective inhibitor of the Na+/H+ exchanger 3 (NHE3) with IC50 of 5 and 10 nM for human and rat NHE3, respectively. |
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DC8370 |
Teneligliptin hydrobromide
Featured
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Teneligliptin is a novel, potent, and long-lasting dipeptidyl peptidase-4 inhibitor; competitively inhibited human plasma, rat plasma, and human recombinant DPP-4 in vitro, with IC50 values of approximately 1 nM. |
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DC9428 |
Teneligliptin |
Teneligliptin is a novel, potent, and long-lasting dipeptidyl peptidase-4 inhibitor; competitively inhibited human plasma, rat plasma, and human recombinant DPP-4 in vitro, with IC50 values of approximately 1 nM.
IC50 value: 1 nM [1]
Target: DPP4
in vi |
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DCAPI1145 |
Teniposide (Vumon) |
Teniposide (Vumon) |
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DC4156 |
Tenofovir disoproxil fumarate
Featured
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Tenofovir disoproxil fumarate belongs to nucleotide analogue reverse transcriptase inhibitors (nRTIs). |
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DC26022 |
Tenofovir exalidex(CMX157) |
Tenofovir exalidex is a novel lipid acyclic nucleoside phosphonate that delivers high intracellular concentrations of the active antiviral agent tenofovir. |
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DC9780 |
Tenofovir disoproxil
Featured
|
Tenofovir is an antiretroviral drug known as nucleotide analogue reverse transcriptase inhibitors (NRTIs), which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV. |
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DC8926 |
Tenofovir |
Tenofovir(GS 1278, PMPA) is an antiretroviral drug known as nucleotide analogue reverse transcriptase inhibitors (NRTIs), which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV. |
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DC9072 |
Tenoxicam |
Tenoxicam, an antiinflammatory agent with analgesic and antipyretic properties. |
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DC9151 |
Terazosin HCl |
Terazosin Hydrochloride dihydrate is a selective alpha1-antagonist used for treatment of symptoms of benign prostatic hyperplasia (BPH). |
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DC8697 |
Terbuthylazine
Featured
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Terbuthylazine is an inhibitor of acetolactate syntase (ALS), is a selective herbicide. |
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DC8696 |
Terbutryn |
Terbutryn is a selective herbicide and a triazine compound. It is absorbed by the roots and foliage and acts as an inhibitor of photosynthesis. |
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