Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN481749 Retinyl glucoside 136778-12-6
Retinyl-β-D-glucoside is a naturally occurring and biologically active metabolites of vitamin A, which are found in fish and mammals.
YN360826 Lubiprostone 136790-76-6
Lubiprostone is an activator of ClC-2 chloride channels, used in the management of idiopathic chronic constipation.
YN322082 CCK-A receptor inhibitor 1 137004-80-9
CCK-A receptor inhibitor 1 is acholecystokinin A(CCK-A)receptorinhibitor with a bingingIC50 of 340nM.
YN483491 Fructo-oligosaccharide DP11... 137405-36-8
Fructo-oligosaccharide DP11/GF10 belongs to fructooligosaccharides (FOS) with degree of polymerization (DP=11). Fructo-oligosaccharides (FOS) are composed of 10 fructose units linked by (2→1)-β-glycosidic bonds and having ...
YN483492 Fructo-oligosaccharide DP12... 137405-40-4
Fructo-oligosaccharide DP12/GF11 belongs to fructooligosaccharides (FOS) with degree of polymerization (DP=12). Fructo-oligosaccharides (FOS) are composed of 11 fructose units linked by (2→1)-β-glycosidic bonds and having ...
YN321183 Mozavaptan 137975-06-5
Mozavaptan is a novel competitive vasopressin receptor antagonist for both V1 and V2 receptors with IC50 of 1.2 μM and 14 nM, respectively.
YN481876 Imidacloprid 138261-41-3
Imidacloprid is a nicotinic acetylcholine receptor (nAChR) agonist with potent insecticidal activity.
YN483887 Amylin (8-37), rat 138398-61-5
Amylin (8-37), rat is a truncated analog of native Amylin that selectively inhibits insulin-related glucose uptake and glycogen deposition in muscle tissue. Amylin (8-37), rat is a weakamylin receptor(AMY) antagonist.
YN320578 Mozavaptan hydrochloride 138470-70-9
Mozavaptan hydrochloride (OPC-31260 hydrochloride) is a benzazepine derivative and a potent, selective, competitive and orally activevasopressin V2receptorantagonist with an IC50 of 14nM. Mozavaptan hydrochloride shows ~85-fold...
YN482289 Biotin-DADOO 138529-46-1
Biotin-DADOO is a biotinylation reagent, which can be used to synthesize a biotin-estradiol conjugate (i.e., biotin-DADOO-estradiol) to develop a direct, broad range enzyme immunoassay to measure plasma estradiol concentrations.
YN321827 Galantide 138579-66-5
Galantide, a non-specificgalanin receptorantagonist, is a peptide consisting of fragments of galanin and substance P. Galantide recognizes two classes of galanin binding sites (KD<0.1nM and ~6nM) in the rat hypothalamus. Galanti...
YN481824 Ibandronate Sodium 138844-81-2
Ib and ronate Sodium is a highly potent nitrogen-containing bisphosphonate used for the treatment of osteoporosis.
YN320504 CL 316243 138908-40-4
CL316243 is a highly potent selectiveβ3-adrenoceptoragonist with aEC50of 3nM, but is an extremely poor to β1/2- receptors.CL316243 is a effective stimulant of adipocyte lipolysis and increases brown adipose tissue thermogenesis ...
YN482782 Macranthoidin A 140360-29-8
Macranthoidin A is an orally active saponin fromFlos Lonicerae. Macranthoidin A possess protection effects on hepatic injury caused by Acetaminophen, Cd, and CCl4, and conspicuous depressant effects on swelling of ear croton o...
YN360963 Heteroclitin D 140369-76-2
Heteroclitin D is a lignin from Kadsura medicinal plants with anti-liqid peroxidation. Heteroclitin D inhibits L-typecalcium channels.
RSVA405 is a potent, orally active activator ofAMPK, with an EC50 of 1μM. RSVA405 facilitates CaMKKβ-dependent activation of AMPK, inhibitsmTOR, and promotesautophagyto increase Aβ degradation. RSVA405 ha...
YN483955 [pTyr1146][pTyr1150][pTyr11... 141171-54-2
[pTyr1146][pTyr1150][pTyr1151]Insulin Receptor (1142-1153) binds to insulin and can be used as insulin receptor tyrosine kinase substrates.
YN480298 Lucerastat 141206-42-0
Lucerastat, the galactose form of Miglustat, is an orally-available inhibitor ofglucosylceramide synthase (GCS). Lucerastat has the potential for Fabry disease study.
YN322015 Tarazepide 141374-81-4
Tarazepide is a potent and specificCCK-Areceptor antagonist.
YN1720012 Exendin-4 141758-74-9
Exendin-4 (Exenatide), a 39 amino acid peptide, is a long-actingglucagon-likepeptide-1 receptor agonist with an IC50 of 3.22nM.
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