|Description||Iopamidol is a nonionic, low-osmolar iodinated contrast agent, developed by Bracco.|
|Synonyms||Iopamiro; Isovue; Iopamiron; Niopam|
Alexidine dihydrochloride is a potent and selective protein tyrosine phosphatase localized to the mitochondrion 1(PTPMT1) inhibitor with IC50 value of 1.08 μM i...
Isoalantolactone has the capacity to inhibit tumor cell growth through induction of apoptosis.
17α-Hydroxy Progesterone, as a metabolite of Progesterone, is an endogenous progestogen as well as chemical intermediate in the biosynthesis of other steroid ho...
BMS-212122 is a benzimidazole-based analogue of the potent MTP inhibitor BMS-201038.
BMS 180492, also known as Triazoledione, has been found to be a metabolite of Nefazodone which could be used as an antidepressant for behaving as SERT and NET i...
Sodium formononetin-3'-sulfonate is a water-sol. derivate of formononetin. It has a protective potential against myocardial infarction injury. It not only had f...
Isolated from the seed of Coix lacryma-jobi L. var. meyuan (Romen.) Stapf acts as a central muscle relaxant with an anti-convulsant effect.
Bucetin, a phenacetin analog, has antipyretic and analgesic effect. It has been discontinued for showing renal toxicity.
TUG-905 is a Free Fatty Acid Receptor 4 (FFA4/GPR120) Agonist.
LY 186126 is a potent cGI-PDE inhibitor. It exhibit reversible and high affinity binding to a single class of SaR binding sites.
FDI 6 is an inhibitor of the Forkhead box protein M1 transcription factor (FOXM1) (IC50 value 22.5 µM) that suppresses FOXM1 binding to DNA. FDI6 displaces FOX...
Nanterinone is a novel positive inotropic and balanced-type vasodilating drug partially based on phosphodiesterase III inhibition. It exhibits acute hemodynamic...
AS-35 is used as an antiallergic drug. It controls allergic diseases by inhibiting eosinophil activation.
Rabies Virus Glycoprotein, a 29-amino-acid cell penetrating peptide derived from a rabies virus glycoprotein, is only structural protein of the virus that induc...
MS049 oxalate salt is a potent and selective PRMT4 and PRMT6 inhibitor. MS049 has been shown to reduce the H3R2me2a mark in HEK293 cells with an IC50 value of 0...
NKH477 is a water-soluble analog of forskolin, which is an adenylyl cyclase activator, but it is sparingly soluble in aqueous solutions. It has both inotropic a...
CCF-642 is a protein disulfide isomerase (PDI) inhibitor that exhibits 100-fold higher potency than PACMA 31 (by di-E-GSSG assay) via an alternative mode of act...
FLAG peptide, an eight amino acids peptide with an enterokinase-cleavage site, is a frequently applied hydrophilic and immunogenic fusion tag which was specific...
Valrubicin (AD-32) is a chemotherapy drug used to treat bladder cancer. It is a semisynthetic analog of the anthracycline doxorubicin, and is administered by in...
XE 991 is a KCNQ channel and M-current blocker potentially for the treatment of AD.