Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN480158 (9Z,11E)-Prodlure 50767-79-8
(9Z,11E)-Prodlure ((9Z,11E)-Tetradecadien-1-yl acetate) is the main component of the sex pheromone of femaleSpodoptera littoralis.
YN321625 Amcinonide 51022-69-6
Amcinonide (Cyclocort, CL-34699) is an inhibitor of nitric oxide (NO) release from activated microglia with IC50 of 3.38 nM.
YN321497 Salbutamol hemisulfate 51022-70-9
Salbutamol Sulfate is a short-acting β2-adrenergic receptor agonist with an IC50 of 8.93 ?M.
YN483728 Somatostatin 51110-01-1
Somatostatin is a tetradecapeptide which can suppress the growth hormone (GH) secretion and control the pituitary hormone secretion in human CNS.
YN321944 Substance P (7-11) 51165-05-0
Substance P (7-11) is a C-terminal fragment of Substance P which can cause an increase in the intracellular calcium concentration.
YN321417 Tizanidine 51322-75-9
Tizanidine is an imidazoline derivative and a centrally acting α2 adrenergic agonist used as a muscle relaxant for therapy of acute muscle spasms and chronic spasticity.
YN482416 Soyasaponin Bb 51330-27-9
soyasaponin Bb is a soyasaponin isolated fromPhaseolus vulgaris, acting as analdose reductase differential inhibitor (ARDI).
YN321152 Metoprolol 51384-51-1
Metoprolol is a cardioselective β1-adrenergic blocking agent with log Kd values of −7.26±0.07, −6.89±0.09, −5.16±0.12 for β1, β2, and β3 adrenoceptors, respectively. It is used for acute myocardial infarction, heart failure, an...
YN372893 Alrestatin 51411-04-2
Alrestatin is an inhibitor of aldose reductase which is involved in the pathogenesis of complications of diabetes mellitus, including diabetic neuropathy.
YN320843 Cimetidine 51481-61-9
Cimetidine, a histamine congener, competitively inhibits histamine binding to histamine H2 receptors.
YN321147 Carteolol hydrochloride 51781-21-6
Carteolol HCl is a β-adrenoceptor antagonist, used for the treatment of glaucoma.
YN320589 Angiotensin (1-7) 51833-78-4
Angiotensin 1-7 (Ang-(1-7)) is a major active component of the renin-angiotensin system (RAS), produced from cleavage of Ang II by angiotensin-converting-enzyme type 2 (ACE2). Angiotensin 1-7 inhibits purified canine ACE act...
YN372894 Alrestatin sodium 51876-97-2
Alrestatin sodium is an inhibitor of aldose reductase, an enzyme involved in the pathogenesis of complications of diabetes mellitus, including diabetic neuropathy.
YN270247 Estramustine phosphate sodium 52205-73-9
Estramustine phosphate sodium is an antitumour drug with a unique dual mode of action. Estrone and estradiol, products of the metabolism of estramustine phosphate sodium, have shown antigonadotrophic activity resulting in reduced testoste...
YN321978 Angiotensin II (1-4), human 52580-29-7
Angiotensin II (1-4), human is an endogenous peptide produced from AT I by angiotensin-converting-enzyme (ACE). Angiotensin II binds the AT II type 1 (AT1) receptor, stimulating GPCRs in vascular smooth muscle cells a...
Sevelamer is a phosphate binding drug used to treat hyperphosphatemia in patients with chronic kidney disease; consists of polyallylamine that is crosslinked with epichlorohydrin.
YN320842 Lodoxamide 53882-12-5
Lodoxamide (U-42585E free acid) is an antiallergic compound acting as a mast-cell stabilizer for the treatment of asthma and allergic conjunctivitis.
Tranilast?is an antiallergic drug by inhibiting lipid mediator and cytokine release from inflammatory cells, used for the treatment of allergic disorders such as asthma, allergic rhinitis and atopic dermatitis.
YN320776 Mapenterol hydrochloride 54238-51-6
Mapenterol hydrochloride is a type ofβ2-adrenoceptoragonist.
YN320317 (+)-Cloprostenol 54276-21-0
(+)-Cloprostenol is a prostagl and in F2α (PGF2α) analogue, and shows selective agonistic activity at theprostagl and in receptor.
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