|Description||Hydrochlorothiazide is a diuretic medication often used to treat high blood pressure and swelling due to fluid build up.|
Boldine, an aporphine alkaloid extracted from the leaves and bark of P. boldus, potent antioxidant activity has been linked to anti-inflammatory, anti-pyretic, ...
The deuterium labeled β-Apo-13-carotenone which is an antagonist of RXRα.
ITX-5061 is a scavenger receptor B1 antagonist. Preclinical studies show that ITX-5061 is a selective inhibitor of HCV entry into hepatocytes. It can prevent vi...
IBC 293, a cell-permeable niacin triazolo derivative, is a potent and highly selective agonist for human orphan G-protein-coupled receptor GPR109b/HM74 expresse...
Albitiazolium bromide is a choline analogue acts as a cholinergic receptor antagonists, inhibits choline transport into Plasmodium-infected erythrocytes, thus p...
Collagen proline hydroxylase inhibitor
Collagen proline hydroxylase inhibitor is a collagen proline hydroxylase inhibitor; useful for antifibroproliferative agents.
Aminophenazone (or aminopyrine) is a pyrazolone with analgesic, anti-inflammatory, and antipyretic properties but has risk of agranulocytosis.
L-AP6 is a selective agonist for 'quis'-sensitized site.
CDK2, a member of the eukaryotic S/T protein kinase family, catalyzes the phosphoryl transfer of ATP γ-phosphate to serine or threonine hydroxyl (denoted as S0/...
Betaine,which is isolated from the roots of Beta vulgaris, improves the amplification of DNA by reducing the formation of secondary structure in GC-rich regions...
Mechlorethamine is the prototype of alkylating agents, it works by binding to DNA, crosslinking two strands and preventing cell duplication.
Sasapyrine (salsalate) is a nonsteroidal oral anti-inflammatory agent.Relative to other NSAIDs, salsalate has a weak inhibitory effect on the cyclooxygenase enz...
Napropamid is a selective systemic amide herbicide which is used against a number of annual grasses and broad-leaved weeds for inhibiting root development and g...
Cinepazide maleate is a maleate salt form of cinepazide which is a vasodilator.
Peiminine and DXS significantly reduced alveolar inflammation and pulmonary interstitial inflammation in rats with bleomycin-induced lung injury. peiminine inhi...
Talopram hydrochloride is a potent and selective inhibitor of the noradrenalin transporter (NET) (IC50 = 2.9 nM) that has selectivity for NET against SERT (5-HT...
CH 402 can inhibit lipid peroxidation.
Ro 48-8071 is an orally active cholesterol synthesis inhibitor or a 2,3-oxidosqualene:lanosterol cyclase (OSC) inhibitor. OSC (EC 126.96.36.199) represents a unique ...
UNC-926 is a methyl-lysine (Kme) reader domain inhibitor which binds to the MBT domain of L3MVTL protein (IC50= 3.9 μM).
Bleomycin sulfate is a mixture of the sulfate salts of basic glycopeptide antineoplastic antibiotics isolated from Streptomyces verticillus. Bleomycin sulfate ...