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Endocrinology

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...

  • YN371797 Sevelamer 52757-95-6

    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.

  • YN321419 Tranilast 53902-12-8

    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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