|Description||Gynostemma Extract is a saponins extract derived from the Gynostemma pentaphyllum.|
Beta Carotene is an organic compound and classified as a terpenoid. It is a precursor (inactive form) of vitamin A.
Tomicorat is used as an anti-inflammatory agent.
FG8119 is a novel benzodiazepine agonist.
Cyclandelate is an effective inhibitor of rat hepatic acycloenzyme A: cholesterol acyltransferase (ACAT) with IC50 of 80 μM.
WR 1065 is a metabolite of Amifostine, and a cell-permeable reactive oxygen species scavenger that activates p53 through a JNK-dependent signaling pathway. WR 1...
MK190 is a synthetic bio-active chemical.
CK 869 has been found to inhibit actin polymerization as well as human and bovine actin-related protein 2/3 (Arp2/3) complex.
High affinity aryl hydrocarbon receptor (AhR) agonist (Kd = 70 p M). Proposed to be an endogenous AhR ligand. Induces transient expression of cytochrome P450-1A...
Genz-123346 is a glucosylceramide synthase inhibitor with potential anticancer activity. Exposure of cells to Genz-123346 and to other GCS inhibitors at non-tox...
Hydroxyhexamide, a derivative of acetohexamide, obtained as a pharmacologically active metabolite of acetohexamide. It might be used in the treatment of type 2 ...
Sarolaner is an antiparasitic agent. It is used as veterinary drug.
Racecadotril is a peripherally acting enkephalinase inhibitor with an IC50 of 4.5 μM.
4’-Aminobenzanilide, a significant intermediate, could be widely used in the formation of drugs, dyestuff and agrochemicals.
Procaine is a local anesthetic drug of the amino ester group, which acts through multiple targets.
(Z)-MDL 105519 is the inactive isoform of MDL 105519 which is a high affinity NMDA glutamate receptor antagonist at the glycine site.
WKYMVm is a selective agonist for the formyl peptide receptors FPR1, FPR2 (EC50 = 75 pM) and FPR3 (EC50 = 3 nM) that is expressed on immune cells. WKYMVm induce...
Gadodiamide, a nonionic Gd3+ chelate, is frequently injected i.v. into magnetic resonance imaging (MRI) to enhance contrast.
NAADP tetrasodium salt
NAADP tetrasodium salt is a Ca2+ mobilizing agent. It is an activator of intracellular Ca2+ release via IP3 and cyclic ADP ribose-independent mechanism.
Induces apoptosis. Possible degradation product of taxoid biosynthesis. Anticancer effects.