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Search Results for " secretion "

20

Compounds

Cat No. Product Name Synonyms Targets
T39089 Acid secretion-IN-1
Acid secretion-IN-1, a polycyclic compound, is synthesized for its application as an IDO inhibitor in synthetic experiments.
T10064 LH secretion antagonist 1 Others
LH secretion antagonist 1 is an antagonist of luteinizing hormone secretion with analgesic activity.
T17030 Tegoprazan ATPase , Proton pump
Tegoprazan is a potassium-competitive acid blocker and is a potent, oral active, and highly selective inhibitor of gastric H+/K+-ATPase. That could control gastric acid secretion and motility (IC50: ranging from 0.29-0.5...
T8348 Phentolamine Adrenergic Receptor
Phentolamine mesylate is an alpha-1 and alpha-2 selective adrenergic receptor antagonist
T10860 Col003 HSP
Col003 is a selective and potent inhibitor of Hsp47 and competitively binds to the collagen-binding site on Hsp47 (IC50: 1.8 μM). It can be used for the investigation of fibrosis.
TN1877 Lonicerin Apoptosis , Antibacterial
Lonicerin has antioxidant, anti-arthritic and antifungal activities, it can result in a combination therapy for the treatment of fungal arthritis due to C. albicans infection.
T4985 Neticonazole Hydrochloride Antifungal
Neticonazole Hydrochloride is an imidazole antifungal for the treatment of fungal skin infections. Neticonazole is reported as a potent exosome inhibitor which can block the activity of exosomes.
T1285 Anethole trithione Anetholtrithion Others , AChR
Anethole trithione (Anetholtrithion) is a bile secretion-stimulating drug that restores salivation and relieves the discomfort of dry mouth in chemotherapy-induced xerostomia.
T27527 HBF-0259 HBF 0259 Antiviral
HBF-0259 is an inhibitors of hepatitis B virus surface antigen (HBsAg) secretion with an EC50 of 11.3 μM and a CC50 value of >50 μM in HepG2.2.15 cells. HBF-0259 had a EC50 of approximately 1.5 microM in a secondary, HBV...
T15784 LP99 Epigenetic Reader Domain
LP99 is an epigenetic probe. LP99 disrupts the binding of BRD7 and BRD9 to chromatin in cells. LP99 is an effective and selective inhibitor of the BRD7 and BRD9 bromodomains (Kd: 99 nM against BRD9).
T7127 DC260126 Apoptosis , GPR
DC260126 is a small-molecule antagonist of FFA1 (GPR40)
T1403 Climbazole BAY-e 6975 Antibiotic , Antifungal
Climbazole (BAY-e 6975) is a broad-spectrum imidazole antifungal agent with anti-dandruff benefits.
T9349 IXA4 IRE1
IXA4 is a highly selective, nontoxic activator of IRE1/XBP1s and reduces APP secretion by activating IRE1. IXA4-stimulated IRE1 activation also enhanced pancreatic function.
T6700 Tenatoprazole TU-199 Proton pump
Tenatoprazole (TU-199), a prodrug of the proton pump inhibitor (PPI) class, can inhibit proton transport (IC50: 3.2 μM).
T8798 MSA-2 STING
MSA-2 is a potent and orally available non-nucleotide STING agonist.
T4316 ML365 Potassium Channel
ML365 is a novel selective small molecule inhibitor of TASK1(KCNK3).
T1052 Proglumide cholecystokinin
Proglumide (Binoside) is a cholecystokinin antagonist, which blocks both the CCKA and CCKB subtypes. Proglumide is a drug that exerts an inhibitory effect on gastric secretion and reduces gastrointestinal motility. It is...
T0865 Ranitidine Hydrochloride AH19065 P450 , Antibacterial , Histamine Receptor
Ranitidine Hydrochloride (AH19065) is a member of the class of histamine H2-receptor antagonists with antacid activity. Ranitidine is a competitive and reversible inhibitor of the action of histamine, released by enteroc...
T8599 Betazole dihydrochloride Betazole hydrochloride Histamine Receptor
Betazole dihydrochloride (Betazole hydrochloride) is an agonist of H2 receptor.
T3171 GSK137647A GSK 137647 GPR
GSK137647A (GSK 137647) is a selective FFA4 agonist.
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TargetMol