GlpBio

Angiotensin Receptor

Angiotensin Receptor(血管紧张素受体)

The angiotensin receptors are seven-membrane G-protein-coupled receptors. They mediate the cardiovascular and other effects of angiotensin II which is a bioactive peptide of the renin–angiotensin system.

Angiotensin Receptor 相关产品(111)

  • GC42810 structure
    GC42810Angiotensin II (5-8) (human, rat, mouse)
    CAS: 34233-50-6
    纯度: >95.00%

    An endogenous angiotensin II fragment

  • GC43580 structure
    GC43580DX600
    CAS: 478188-26-0
    纯度: >98.00%

    A peptide inhibitor of ACE2

  • GC45390 structure
    GC45390Benazepril Acyl-β-D-Glucuronide
    纯度: >95.00%

    A metabolite of benazepril

  • GC45501 structure
    GC45501Lisinopril-d5
    CAS: 1356905-39-9
    纯度: >99.00%

    An internal standard for the quantification of lisinopril

  • GC46155 structure
    GC46155H-Ile-Pro-Pro-OH (trifluoroacetate salt)
    纯度: >95.00%

    具有多种生物活性的神经肽

  • GC46233 structure
    GC46233Trandolaprilat (hydrate)
    CAS: 951393-55-8
    纯度: >95.00%

    An ACE inhibitor

  • GC46913 structure
    GC46913Benazepril-d5 (hydrochloride)
    CAS: 1279026-26-4
    纯度: >99.00%

    An internal standard for the quantification of benazapril

  • GC47371 structure
    GC47371Fosinopril-d7 (sodium salt)
    CAS: 1217819-83-4
    纯度: >99.00%

    An internal standard for the quantification of fosinopril

  • GC47438 structure
    GC47438H-Val-Pro-Pro-OH (trifluoroactetate salt)
    纯度: >95.00%

    A neuropeptide with diverse biological activities

  • GC48513 structure
    GC48513Quinapril-d5
    CAS: 1279029-79-6
    纯度: >99.00%

    An internal standard for the quantification of quinapril

  • GC49228 structure
    GC49228Ganoderol B
    CAS: 104700-96-1
    纯度: >95.00%

    A triterpenoid with diverse biological activities

  • GC49408 structure
    GC49408Ramipril Diketopiperazine Acid
    CAS: 108736-10-3
    纯度: >95.00%

    A potential impurity found in commercial preparations of ramipril

  • GC49566 structure
    GC49566DX600 (trifluoroacetate salt)
    纯度: >98.00%

    A peptide inhibitor of ACE2

  • GC49653 structure
    GC49653Ramipril Diketopiperazine
    CAS: 108731-95-9
    纯度: >95.00%

    A potential impurity found in commercial preparations of ramipril

  • GC60095 structure
    GC60095Brain Natriuretic Peptide (1-32), rat acetate
    纯度: >99.50%

    BrainNatriureticPeptide(1-32),ratacetate(BNP(1-32),ratacetate)是一种含有32个氨基酸的多肽。可作为心力衰竭病人病残率和死亡率的生化标志。

  • GC60584 structure
    GC60584Angiotensin II human acetate
    CAS: 68521-88-0
    纯度: {{1-5}>99.00% / {6-13}>98.00%}

    A peptide hormone

  • GC60748 structure
    GC60748Dehydro Olmesartan
    CAS: 172875-98-8

    DehydroOlmesartan是Olmesartan的衍生物。Olmesartan是血管紧张素II受体(AT1R)拮抗剂，可用于高血压的研究。

  • GC61153 structure
    GC61153Olmesartan medoxomil impurity C
    CAS: 879562-26-2

    OlmesartanmedoxomilimpurityC是Olmesartanmedoxomil的杂质。Olmesartanmedoxomil是一种有效的选择性的血管紧张素(angiotensinAT1)受体抑制剂，IC50为66.2μM。

  • GC61154 structure
    GC61154Olmesartan methyl ester
    CAS: 1347262-29-6

    Olmesartanmethylester是Olmesartanmedoxomil合成的中间体。Olmesartanmedoxomil是一种有效的选择性的血管紧张素(angiotensinAT1)受体拮抗剂，IC50为66.2μM。

  • GC61496 structure
    GC61496Angiotensin (1-7) (acetate)
    CAS: 2855063-75-9
    纯度: >98.50%

    Angiotensin (1-7) (Ang-(1-7), Angiotensin fragment 1-7) is a bioactive component of the renin-angiotensin system that is formed endogenously from either Ang I or Ang II. Angiotensin (1-7) is a canine ACE inhibitor with an IC50 of 0.65 μM and inhibits the activity mediated by myostatin through Mas receptor.

  • GC61952 structure
    GC61952Angiotensin I/II (1-6) (TFA)
    纯度: >98.50%

    Angiotensin I/II (1-6) TFA 含有 1-6 个氨基酸，由血管紧张素 I/II 肽转化而来。前体血管紧张素原被肾素裂解形成 Angiotensin I。Angiotensin I 被血管紧张素转换酶 (ACE)水解形成具有生物活性的 angiotensin II。Angiotensin II 用于高血压、肾素-血管紧张素系统和特发性膜性肾病的研究。

  • GC62844 structure
    GC62844Angiotensin II human TFA
    CAS: 2761969-44-0
    纯度: >99.50% / >98.00%

    Angiotensin II human (Angiotensin II) TFA 是一种血管收缩剂，是肾素/血管紧张素系统的主要生物活性肽。Angiotensin II human TFA 在调节人类血压中起着核心作用，主要通过血管紧张素 II 与 G 蛋白偶联受体 (GPCRs)、血管紧张素II 1型受体 (AT1R) 和血管紧张素II 2型受体 (AT2R) 之间的相互作用来介导。Angiotensin II human TFA 刺激交感神经刺激，增加醛固酮生物合成和肾脏活动。Angiotensin II human TFA 诱导血管平滑肌细胞生长，增加成纤维细胞中 I 型和 III 型胶原的合成，导致血管壁和心肌增厚，并导致纤维化。Angiotensin II human TFA 也诱导细胞凋亡。Angiotensin II human TFA 通过 LOX-1 依赖的氧化还原敏感途径诱导内皮细胞毛细血管形成。

  • GC63298 structure
    GC63298Ganoderic acid N
    CAS: 110241-19-5
    纯度: >98.00%

    A triterpene with ACE inhibitory activity

  • GC64604 structure
    GC64604Mopivabil
    CAS: 2988562-84-9
    纯度: >99.00%

    Mopivabil 是血管紧张素 II 受体 (angiotensin II receptor) 的拮抗剂。