|Description||Meclofenoxate (Lucidril), also known as centrophenoxine, is a drug used to treat the symptoms of senile dementia and Alzheimer's disease. It is an ester of dimethylethanolamine (DMAE) and 4-chlorophenoxyacetic acid (pCPA). DMAE is a natural substance, found especially in fish. pCPA is a synthetic compound that resembles a variety of plant hormones called auxins.|
Kaempferol is a natural flavonol, a type of flavonoid, that has been isolated from plant sources.
Genistinis, a derivative of Genistein, is selective inhibitor of mammalian terminal deoxynucleotidyl transferase.
O4I2 is a potent inducers of Oct3/4. O4I2 showed high activity in enforcing Oct3/4 expression. O4I2 is a new class of small molecules suitable for iPSC generati...
Kisspeptin-10, also called as Metastin (45-54), is a potent vasoconstrictor and a potent endogenous ligand for the Kisspeptin receptor (KISS1, GPR54).
The deacetylated of BMS-202 which is a small-molecule PD-1/PD-L1 interaction inhibitor (IC50= 18 nM).
The hydrochloride salt form of Oxyphencyclimine which could influence the peripheral parasympathetic system and increase the stomach secretions.
KF 13218, a novel pyridobenzazepinone derivative, inhibited human and bovine platelet thromboxane synthase with IC50 values of 27 +/- 5.8 nmol/l (mean +/- S.E.M...
ATR-101 is a selective Acetyl CoA C-acetyltransferase inhibitor. ATR-101 is uniquely distributed to adrenal tissues and inhibition of adrenal ACAT1 by ATR-101 d...
CP-69799 is an inhibitor of aspartate proteinases.
GK921 is a transglutaminase 2 (TGase 2) inhibitor with average GI50 of 0.9 μM in cancer cell lines.
Desmopressin acetate, also know as DDAVP, has been found to be a vasopressor agent that could exhibit antidiuretic activity and probably be useful in improving ...
Dexmecamylamine is a nicotinic channel modulator with antidepressant activity. It demonstrated positive effects in a number of animal models of depression and a...
A metabolite of acetaminophen, which is is a pain reliever and a fever reducer.
Athidathion(GS-13006) is an organophosphate insecticide.
666-15 is a potent and selective inhibitor of CREB-mediated gene transcription (IC50= 81 nM) with efficacious in vitro and in vivo anti-breast cancer activity w...
Etebenecid, a benzenesulfonic acid derivative, could be used to reduce uric acid levels acting as a uricosuric agent.
T-3364366 is a reversible and slow-binding Delta-5 desaturase (D5D) inhibitor. Ki is less than 2.7 nM and a dissociation half-life is more than 2.0 h. D5D is an...
This active molecular is a potent cephalosporin antibiotic with a catechol moiety on the 3-position side chain under the development of Shionogi. Cefiderocol ex...
AI-10-49 is a protein-protein interaction inhibitor that selectively binds to CBFβ-SMMHC and disrupts its binding to RUNX1 with a FRET IC50 of 0.26 uM.