Cat. No. | Product Name | Field of Application | Chemical Structure |
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DC22347 | Penciclovir Featured |
A guanosine analogue antiviral agent used for the treatment of various herpesvirus (HSV) infections.
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DC9843 | AKR1C3 Inhibitor 5f Featured |
A highly potent and selective inhibitor of the type 5 17-β-hydroxysteroid dehydrogenase AKR1C3.
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DCAPI1496 | Ambrisentan Featured |
A nonpeptide endothelin ETA receptor antagonist. Antihypertensive.
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DC8784 | CTLA-4 inhibitor Featured |
A novel CTLA-4 inhibitor.
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DC10706 | Ehp-inhibitor-2 Featured |
A novel Ehp inhibitor
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DC10705 | Ehp-inhibitor-1 Featured |
A novel Ehp inhibitor
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DC10801 | AMPA/kainate antagonist-1 Featured |
A novel Non-competitive AMPA/kainate antagonist.
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DC24203 | P2X2/3 receptor antagonist Featured |
A novel P2X3 and P2X2/3 receptor antagonist useful for the treatment
of urinary tract diseases, pain, respiratory diseases and cardiovascular diseases.
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DC23094 | TRAP-6 Featured |
A PAR1 peptide fragment (residues 42-47) that acts as a PAR1 agonist.
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DC22890 | Frovatriptan Featured |
A potent, long lasting 5-HT(1B/1D) receptor agonist as a antimigraine agent..
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DC21560 | RC-3095 Featured |
RC-3095 is a gastrin-releasing peptide receptor antagonist, synergizes with gemcitabine to inhibit the growth of human pancreatic cancer CFPAC-1 in vitro and in vivo. RC-3095 inhibit the growth of human glioblastomas in vitro and in vivo. RC3095 inhibits tumor growth and decrease the levels and mRNA expression of epidermal growth factor receptors in H-69 small cell lung carcinoma.R,BRS-1) antagonist.
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DC22348 | Zalcitabine Featured |
A pyrimidine analog reverse transcriptase inhibitor (NRTI) for the treatment of HIV/AIDS.
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DC7149 | GW1929 Featured |
GW1929 is a synthetic peroxisome proliferator-activated receptor-γ (PPARγ) agonist with IC50 of 6.2 nM and 13 nM for human and mouse, respectively.
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DC23965 | Clopidogrel thiolactone Featured |
A thienopyridine-class antiplatelet agent that works by irreversibly inhibiting P2Y12 receptor on platelets.
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DC8475 | A-1210477 Featured |
A-1210477 is a potent and selective MCL-1 inhibitor.
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DC12659 | A-381393 Featured |
A-381393 is a potent and selective agonist of the dopamine D4 receptor.
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DC22277 | A-420983 Featured |
A-420983 is a potent, orally active inhibitor of lck with efficacy in a model of transplant rejection.
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DC8161 | Xeglyze(Abametapir) Featured |
Abametapir is the active ingredient of Xeglyze Lotion.
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DC24211 | Abiraterone (D4A) Featured |
Abiraterone (D4A) is an active metabolite of the CYP17A1 inhibitor abiraterone.
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DC7352 | ABT-333 Featured |
ABT-333 is an NS5B non-nucleoside polymerase inhibitor.
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DC10049 | Tebanicline(ABT-594) Featured |
ABT-594 represents a novel class of broad-spectrum analgesics whose primary mechanism of action is activation of the neuronal nicotinic acetylcholine receptors.
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DC9262 | ABT-719 Featured |
ABT-719 is a potent bacterial DNA gyrase inhibitor.
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DC9261 | ABT-719 HCl Featured |
ABT-719 is a potent bacterial DNA gyrase inhibitor.
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DC1022 | ABT-737 Featured |
ABT-737 is a BH3 mimetic inhibitor of Bcl-xL, Bcl-2 and Bcl-w with EC50 of 78.7 nM, 30.3 nM and 197.8 nM, respectively.
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DC11183 | ABX-1431 hydrochloride Featured |
ABX-1431 (ABX1431) is a highly potent, selective, orally available, CNS-penetrant monoacylglycerol lipase (MGLL) with IC50 of 14 nM (hMGLL).
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DC12577 | AC-263093 Featured |
AC-263093 (AC263093) is a potent, functionally selective neuropeptide FF receptor type 2 (NPFFR2) agonist with pKi of 6.9.
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DC12492 | N-(p-Amylcinnamoyl) anthranilic Acid (ACA) Featured |
ACA is a cell permeable inhibitor of PLA2,reported to inhibit α-ketoisocaproic acid and glyceraldehyde-induced insulin secretion, as well as glucose-induced insulin secretion.
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DC9917 | Acacetin Featured |
Acacetin is an O-methylated flavone found in Robinia pseudoacacia (black locust), Turnera diffusa (damiana),Betula pendula (silver birch),and in the fern Asplenium normale.
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DC22280 | Acarbose Featured |
Acarbose is the first identified α-glucosidase inhibitor.
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DC9986 | Acebilustat(ZK322) Featured |
Acebilustat(ZK322) is a potent and selective leukotriene A4 hydrolase inhibitor.
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