|Description||Carbetocin is a potent agonist of the oxytocin receptor, with improved in vivo stability over oxytocin.|
|Synonyms||Duratocin; Pabal; Lonactene|
Kallikrein Inhibitor, a synthetic peptide, is a serine protease inhibitor that inhibits kallikrein and plasmin, and can attenuate breast cancer cell invasion.
Glyparamide is a chlorophenyl-containing sulfonylurea with hypoglycemic activity and rarely causes hepatic injury.
Etidronate (Didronel) is a human protein tyrosine phosphatase inhibitor with IC50 of 0.2 μM.
This compound is a bio-active molecular, but no detailed information has been published yet.
LH secretion antagonist 1
An antagonist of luteinising hormone secretion
N-Desmethyl Ivabradine HCl
The hydrochloride salt form of N-Desmethyl Ivabradine which is an derivative of Ivabradine generated through metabolism.
Cyclamic acid in the form of its sodium or calcium salt is one of the most widely used artificial sweeteners.
Eicosapentaenoic acid (EPA) is an omega-3 fatty acid.
W-54011 is a potent, specific high affinity C5a receptor antagonist (Ki = 2.2 nM).
Sagittatoside B is a natural compound isolated from traditional Chinese herb Yinyanghuo (Herba Epimdii).
(R)-GNE-140 is a potent lactate dehydrogenase A (LDHA) inhibitor (IC50s= 3 nM for LDHA and 5 nM for LDHB), with 18-fold more potent than S enantiomer.
Halcinonide is a high potency corticosteroid used in topical preparations as an anti-inflammatory agent.
Omeprazole sulphide is a metabolite of Omeprazole. It is an intermediate used in the production of the gastric proton pump inhibitors, omeprazole and esomeprazo...
Auranofin appears to induce heme oxygenase 1 (HO-1) mRNA, as an inhibitor of thioredoxin reductase (TrxR) (IC50 = 20 nM; Ki = 4 nM for the NADPH-reduced form of...
Atosiban, a nonapeptide, desamino-oxytocin analogue, is a competitive inhibitor of the hormones oxytocin and vasopressinv. It inhibits the oxytocin-mediated rel...
Dexmecamylamine is a nicotinic channel modulator with antidepressant activity. It demonstrated positive effects in a number of animal models of depression and a...
Peiminine and DXS significantly reduced alveolar inflammation and pulmonary interstitial inflammation in rats with bleomycin-induced lung injury. peiminine inhi...
SPDB, a pyridyldithioyl compound, has been found to link to DM4 conjugates and probably influence the releasement of cytotoxic metabolitesin.
Formononetin is a phytoestrogen from the root of Astragalus membranaceus and an O-methylated isoflavone.
FR-181157, an oxazol derivative, has been found to be a prostaglandin mimetic and could have potential biological activities as a IP receptor agonist.