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Cat. No. Product Name Field of Application Chemical Structure
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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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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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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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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DC10592 ASL 601(Acecainide) Featured
Acecainide, also known as N-acetylprocainamide and ASL 601, is the N-acetylated metabolite of procainamide.
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DC8798 Acotiamide Featured
Acotiamide acts as an acetylcholinesterase inhibitor
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DC11512 Acrizanib Featured
Acrizanib(LHA510) is a potent and selective angiogenesis inhibitor and VEGFR‑2 Inhibitor Specifically Designed for Topical Ocular Delivery, as a Therapy for Neovascular Age-Related Macular Degeneration.
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DC10492 ACSS2 inhibitor Featured
ACSS2 inhibitor is a novel ACSS2 inhibitor.
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DC7997 ACTB-1003 Featured
ACTB-1003 is a potent inhibitor of FGFR1 with IC50 <10 nM in FGFR-1 biochemical assay; more information can be find in Patent WO/2007/064883A2, Example 12.
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