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Endocrinology

Chemical structure

Cat.No.

Product Name

CAS no.

Target

  • YN321361 Tasosartan 145733-36-4

    Tasosartan is a long-actingangiotensin II(AngII)receptorantagonist.

  • YN320785 Goserelin acetate 145781-92-6

    Goserelin is a luteinizing hormone releasing hormone (LHRH) agonist, which is used to suppress production of the sex hormones.

  • YN370065 MSDC 0160 146062-49-9

    MSDC 0160 (Mitoglitazone) is a mitochondrial target of thiazolidinediones (mTOT)-modulatinginsulin sensitizer and a modulator ofmitochondrial pyruvate carrier (MPC). MSDC 0160 is a thiazolidinedione (TZD) with antidiabeti...

  • YN320220 ZD 7155(hydrochloride) 146709-78-6

    ZD 7155 hydrochloride is an angiotensin II receptor type 1 (AT1 receptor) antagonist.

  • YN321110 Alcaftadine 147084-10-4

    Alcaftadine is a high affinity ligand for the H1 receptor, with a pKi (8.5) that is comparable with that of other H1 antihistamines. Alcaftadine is also an antagonist for H2 and H4 receptors with no affinity for the H3 receptor.

  • YN320054 Maropitant 147116-67-4

    Maropitant is a selective and orally activeneurokinin (NK1) receptorantagonist. Maropitant acts by blocking the binding of substance P within the emetic center and the chemoreceptor trigger zone (CRTZ). Maropitant is highly ef...

  • YN320931 Azilsartan 147403-03-0

    Azilsartan is an angiotensin II type 1 (AT1) receptor antagonist with IC50 of 2.6 nM.

  • YN321323 Bosentan 147536-97-8

    Bosentan is a competitive and dual antagonist ofendothelin-1 (ET)for the ETA and ETBreceptors with Kiof 4.7nM and 95nM in human SMC, respectively.

  • YN322028 MG 1 148274-76-4

    MG 1 is an α1adrenergic receptorantagonist.

  • YN321806 Substance P TFA 148470-19-3

    Substance P TFA (Neurokinin P TFA) is a neuropeptide, acting as a neurotransmitter and as a neuromodulator in the CNS. The endogenous receptor for substance P isneurokinin 1 receptor(NK1-receptor,NK1R).

  • YN321399 Ivabradine hydrochloride 148849-67-6

    Ivabradine HCl, a new If inhibitor with IC 50 of 2.9 μM which acts specifically on the pacemaker activity of the sinoatrial node, is a pure heart rate lowering agent.

  • YN320178 QF0301B 149247-12-1

    QF0301B is anα1 adrenergic receptorantagonist and a low α2 adrenoceptor, 5-HT2A, and histamine H1 receptor blocker.

  • YN373976 CGP-53153 149281-19-6

    CGP-53153 is a steroidal inhibitor of5 alpha reductasewith IC50s of 36 and 262nM in rat and human prostatic tissue, respectively.

  • YN321210 Elisartan 149968-26-3

    Elisartan is an orally active non-peptide pro-drug ofangiotensin II AT1 receptorantagonist HN-12206, and shows anti-hypertension activities.

  • YN321207 Terbogrel 149979-74-8

    Terbogrel is an orally availablethromboxane A2 receptorantagonist and athromboxane A2 synthaseinhibitor, with bothIC50s of about 10nM.

  • YN321100 Tolvaptan 150683-30-0

    Tolvaptan is an orally effective nonpeptide arginine vasopressin V2 receptor antagonist with IC50 of 3 nM, used to treat hyponatremia.

  • YN321228 Ro 46-2005 150725-87-4

    Ro 46-2005 is a novel synthetic non-peptide endothelin receptor antagonist, inhibits the specific binding of 125I-ET-1 to human vascular smooth muscle cells (ETA receptor) with IC50 of 220nM.

  • YN484010 Phosphorylase Kinase β-Sub... 150829-21-3

    Phosphorylase Kinase β-Subunit Fragment (420-436) is the β-Subunit fragment (peptide 430-436) of phosphorylase kinase. Phosphorylase kinase is a serine/threonine-specific protein kinase which activates glycogen phosphorylase to rele...

  • YN321427 Nebivolol hydrochloride 152520-56-4

    Nebivolol HCl selectively inhibits β1-adrenoceptor with IC50 of 0.8 nM.

  • YN321579 Fexofenadine hydrochloride 153439-40-8

    Fexofenadine inhibits histamine H1 receptor with IC50 of 246 nM.

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