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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8348 | Phentolamine | Adrenergic Receptor | |
Phentolamine mesylate is an alpha-1 and alpha-2 selective adrenergic receptor antagonist | |||
T35862 | Cucurbit[8]uril | Others | |
Cucurbit[8]uril is a highly effective and safe supramolecular compound that promotes protein heterodimerization. It selectively induces the heterodimerization of methylviologen and naphthalene functionalized proteins, de... | |||
T8345 | Carbutamide | Others | |
Carbutamide is a sulfonylurea antidiabetic agent with hypoglycemic activity. | |||
T8580 | Bupranolol | Adrenergic Receptor | |
Bupranolol is an antagonist of β2-adrenergic receptor and has been used for angina pectoris, hypertension, glaucoma, cardiac arrhythmia and as an antithrombotic. | |||
T9565 | OSBPL7-IN-1 | Others | |
OSBPL7-IN-1 is an orally active inhibitor of oxysterol binding protein like 7 (OSBPL7). OSBPL7-IN-1 promotes an increase of ABCA1 at the plasma membrane without affecting mRNA expression[1]. | |||
T9692 | Paltusotine | Somatostatin | |
Paltusotine is a nonpeptide, small molecule somatostatin type 2 (SST2) receptor agonist with high oral bioavailability. Paltusotine maintains GH and IGF-1 levels in acromegaly patients | |||
T9732 | VY-3-135 | Fatty Acid Synthase | |
VY-3-135 is a metastasis inhibitor and an acetyl-CoA synthetase 2 (ACSS2) modulator. | |||
T1292 | Tiapride hydrochloride | Dopamine Receptor | |
Tiapride is a selective blocker of D2/3 dopamine receptors in the brain. It is used in the therapy of various psychiatric and neurological disorders containing dyskinesia, negative symptoms of psychosis, alcohol withdraw... | |||
T8734 | Choline | Others | |
Choline is a ubiquitous water soluble nutrient, often associated with the B vitamins | |||
T34896 | Tofisopam | Emandaxin,Grandaxin | Others |
Tofisopam (Grandaxin) is a 2,3-benzodiazepine compound with anxiolytic activity that can be taken orally. | |||
T15500 | HPi1 | Others , Antibacterial | |
HPi1 is a selective and orally active antimicrobial against Helicobacter pylori (IC50: 0.24 μM and a MIC of 0.08-0.16 μg/mL). HPi1 is inactive against other Xaliproden, including the gut commensals, Lactobacillus reuteri... | |||
T9346 | CVN424 | GPR | |
CVN424 is a selective and novel GPR6 Inverse agonist effective in models of Parkinson Disease. | |||
T16115 | MLi-2 | LRRK2 | |
MLi-2 is a structurally novel, highly potent, and selective LRRK2 kinase inhibitor with central nervous system activity. MLi-2 exhibits exceptional potency in a purified LRRK2 kinase assay in vitro (IC50 = 0.76 nM), a ce... | |||
T3306 | PF-04418948 | PF 04418948,PF04418948 | Prostaglandin Receptor |
PF-04418948 is a potent EP2 receptor antagonist (IC50 = 16 nM for human EP2 receptors). Displays over 2000-fold selectivity for EP2 receptors over EP1, EP3, EP4, DP1 amd CRTH2 receptors; exhibits <30% binding at a divers... | |||
TN2081 | Maohuoside A | MAPK | |
Maohuoside A promotes osteogenesis of rat mesenchymal stem cells via BMP and MAPK signaling pathways. | |||
T9214 | ELOVL6-IN-1 | Others | |
ELOVL6-IN-1 is a potent, orally active and selective ELOVL6 inhibitor. ELOVL6-IN-1 dose-dependently inhibits mouse ELOVL6 activities, with an IC50 value of 0.350 μM. ELOVL6-IN-1 inhibits ELOVL6 in a noncompetitive manner... | |||
T9683 | VX-150 | Sodium Channel | |
VX-150 is a highly selective NaV1.8 inhibitor relative to the other sodium channel subtypes (>400-fold). | |||
T9215 | ELOVL6-IN-2 | Others | |
ELOVL6-IN-2 is a orally active and selective ELOVL6 inhibitor. | |||
T2013 | Ponalrestat | Reductase | |
Ponalrestat is an aldose reductase inhibitor. | |||
T39695 | ARD-2128 | Androgen Receptor | |
ARD-2128 is a highly potent, orally bioavailable PROTAC (proteolysis-targeting chimera) degrader of the androgen receptor (AR), effectively diminishing AR protein levels, suppressing AR-regulated gene expression in tumor... |