Chemical structure
Cat.No.
Product Name
CAS no.
Target
Tiaprost is a prostagl and in F2α(PGF2α) analogue.
YN320250 Bucindolol 71119-11-4
Bucindolol is aβ1-adrenergic receptorblocker, with intrinsic sympathomimetic activity, used in the research of heart failure.
D2343 is aβ2-adrenoceptoragonist and also is anα1- adrenoceptorinhibitor.
YN320811 ICI 118,551 hydrochloride 72795-01-8
ICI 118,551 (hydrochloride) is a highly selectiveβ2 adrenergic receptorantagonist, with Kis of 0.7, 49.5 and 611nM for β2, β1 and β3 receptors, respectively.
BW 245C is aprostanoid DP-receptor (DP1)agonist, used to treat stroke.
YN321355 Dapiprazole hydrochloride 72822-13-0
Dapiprazole Hydrochloride is the hydrochloride salt form of dapiprazole, an alpha-adrenergic blocker used to reverse mydriasis after eye examination.
YN320198 Lidanserin 73725-85-6
Lidanserin (ZK-33839) acts as a5-HT2A and α1-adrenergic receptorantagonist.
Doxazosin is a quinazoline-derivative that selectively antagonizes postsynaptic α1-adrenergic receptors.
YN320783 Leuprolide Acetate 74381-53-6
Leuprolide acetate is a synthetic nonapeptide that is a potent gonadotropin-releasing hormone receptor (GnRHR) agonist used for diverse clinical applications, including the treatment of prostate cancer, endometriosis, uterine fibroids,...
Sauvagine, a 40-amino-acid neuropeptide from the skin of the frog, is amammalian CRFagonist. Sauvagine is effective at releasing ACTH from rat pituitary cells. Sauvagine possesses a number of pharmacological actions on diuresis, t...
AZ-1355 is an effctive lipid-lowering compound, which also inhibits platelet aggregation in vivo and elevates the prostagl and in I2/thromboxane A2ratio in vitro.
YN320665 Cefminox sodium 75498-96-3
Cefminox Sodium is the sodium salt form of cefminox, a semi-synthetic, second-generation, beta-lactamase-stable cephalosporin with antibacterial activity.
Ancarolol is abeta-adrenergicblocking agent.
YN321804 Pancreatic Polypeptide, huma... 75976-10-2
Pancreatic Polypeptide, human is a C-terminally amidated 36 amino acid peptide, which acts as aneuropeptide Y(NPY)Y4/Y5receptor agonist.
SCH28080 is a reversible, K+-competitive inhibitor of thegastric (H+/K+)-ATPase, with a Ki of 0.12μM. SCH28080 is an effective inhibitor of acid secretion in vivo and with anti-gastric ulcer activity .
KP136 (AL136) is an orally effective antiallergic agent. TheIC50is 76.1 μg/mL forhistamine release and 63 ug/mL fordegranulation.
YN321402 Detomidine 76631-46-4
Detomidine, an imidazole derivative, is a potentα2-adrenergicagonist. Detomidine produces dose-dependent sedative and analgesic effects.
YN321471 Famotidine 76824-35-6
Famotidine is a histamine H2–receptor antagonist with IC50 of 0.6 mM, commonly used to treat heartburn, GERD, ulcers, and other digestive conditions.
YN321449 Nizatidine 76963-41-2
Nizatidine is a histamine H2 receptor antagonist with IC50 of 0.9 nM, also inhibits AChE with IC50 of 6.7 μM.
YN370156 Thyroxine sulfate 77074-49-8
Thyroxine sulfate is a thyroid hormone metabolite.
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