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Endocrinology

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN321968 Mini Gastrin I, human 54405-27-5

    Mini Gastrin I, human is a shorter version of human gastrin, consists of amino acids 5-17 of the parent peptide.

  • YN320362 Cloprostenol sodium salt 55028-72-3

    Cloprostenol sodium salt (ICI 80996 sodium salt) is a potent synthetic prostagl and in analogue, acts as a luteolytic agent , and is aPGF2α receptoragonist.

  • YN320022 Pirolate 55149-05-8

    Pirolate is ahistamine H1receptor.

  • YN320997 WZ811 55778-02-4

    WZ811 is a highly potent competitive CXCR4 antagonist with EC50 of 0.3 nM.

  • YN321154 Metoprolol Tartrate 56392-17-7

    Metoprolol Tartrate is a selective β1 receptor blocker medication, used to treat hypertension and heart failure.

  • YN322105 Tulobuterol hydrochloride 56776-01-3

    Tulobuterol is a long-acting β2-adrenergic receptor agonist that has bronchodilatory, anti-inflammatory, and antiviral activities.

  • YN483884 Calcitonin, eel 57014-02-5

    Calcitonin, eel is the thyroid hormone peptide that contributes to the regulation of calcium homeostasis, widely used in the research of postmenopausal osteoporosis.

  • YN321479 Naftopidil 57149-07-2

    Naftopidil is a selective α1-adrenergic receptor antagonist with Ki of 3.7 nM, 20 nM, and 1.2 nM for α1a, α1b, and α1d, respectively, used for the treatment of benign prostatic hyperplasia.

  • YN321950 [Nle11]-Substance P 57462-42-7

    [Nle11]-Substance P is a substance P analog that avoids methionine oxidation problems.

  • YN321279 HOKU-81 58020-43-2

    HOKU-81 (4-Hydroxytulobuterol) is one of the metabolites of Tulobuterol (HY-B1810). HOKU-81 is a potent and selectiveβ2-adrenoceptorstimulant. HOKU-81 has bronchodilating effect.

  • YN320028 MK-447 58456-91-0

    MK-447 is a free radical scavenger, also a nonsteroidal antiinflammatory agent, and enhances the formation of the endoperoxide, PGH2, and otherprostagl and ins.

  • YN321360 Carboprost tromethamine 58551-69-2

    Carboprost tromethamine is the synthetic 15-methyl analogue of prostagl and in F2α. Carboprost tromethamine can effectively promote law contraction of the uterus and significantly reduce the amount of bleeding during and after deliv...

  • YN321509 Azelastine 58581-89-8

    Azelastine is a potent, second-generation, selective, histamine antagonist.

  • YN480281 Nomegestrol acetate 58652-20-3

    Nomegestrol acetate is a potent, highly selective progestogen, which is characterized as a full agonist at theprogesterone receptor, with no or minimal binding to other steroid receptors, including the and rogen and glucocorticoid recep...

  • YN480280 Nomegestrol 58691-88-6

    Nomegestrol is a potent and orally available progestin, acts as a selective fullprogesterone receptoragonist, with aKdof 5.44nM for rat uterine progesterone receptor, and has moderate anti and rogenic activity and strong antiestrog...

  • YN320258 SB297006 58816-69-6

    SB297006 is aCCR3antagonist, which significantly inhibits proliferation and neurosphere formation in CCL11-treated neural progenitor cells.

  • YN320475 H-Val-Pro-Pro-OH 58872-39-2

    H-Val-Pro-Pro-OH, a milk-derived proline peptides derivative, is an inhibitor of Angiotensin I converting enzyme(ACE), with an IC50 of 9μM.

  • YN322008 Pamatolol 59110-35-9

    Pamatolol is a cardioselectivebeta-adrenoceptorantagonist without sympathomimetic activity.

  • YN482919 Lindleyin 59282-56-3

    Lindleyin, isolated fromRhei rhizoma, mediates hormonal effects through estrogen receptors. Lindleyin binds toERαwith estrogenic activity.

  • YN483892 α-Factor Mating Pheromone,... 59401-28-4

    α-Factor Mating Pheromone, yeast is a tridecapeptide secreted byS. cerevisiaeα cells viaSte2preceptor.

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