ACE

ACE(血管紧张素转换酶)

ACE, also known as angiotensin-converting enzyme, indirectly increases blood pressure by converting angiotensin I to angiotensin II and subsequently constricting the vessels.

ACE 相关产品(73)

  • GC15493 structure
    GC15493Enalaprilat Dihydrate
    CAS: 84680-54-6
    纯度: >98.00%

    Enalaprilat Dihydrate是一种具有口服活性的血管紧张素转换酶(ACE)抑制剂,在体内可迅速水解为活性代谢物Enalaprilat,Enalaprilat通过抑制血管紧张素II的生成,有效舒张血管,降低血压,并减轻心脏负荷。

  • GC15760 structure
    GC15760Ramipril
    CAS: 87333-19-5
    纯度: >98.00%

    A prodrug from of ramiprilat

  • GA20760 structure
    GA20760Angiotensin A (1-7)
    CAS: 1176306-10-7
    纯度: >98.50%

    血管紧张素 A (1-7) 是肾素-血管紧张素系统 (RAS) 的成员,是一种血管活性肽,是 G 蛋白偶联受体 MrgD 的内源性配体。

  • GC10142 structure
    GC10142Enalapril Maleate
    CAS: 76095-16-4
    纯度: >99.50%

    An ACE inhibitor

  • GC10694 structure
    GC10694Ramiprilat
    CAS: 87269-97-4

    An ACE inhibitor

  • GC11228 structure
    GC11228Benazepril
    CAS: 86541-75-5
    纯度: >98.00%

    贝那普利,一种血管紧张素转换酶抑制剂,是一种用于治疗高血压的药物。

  • GC11266 structure
    GC11266Lisinopril dihydrate
    CAS: 83915-83-7
    纯度: >99.50%

    An ACE inhibitor

  • GC11560 structure
    GC11560Resorcinolnaphthalein
    CAS: 41307-63-5
    纯度: >98.50%

    Activator of ACE2

  • GC11655 structure
    GC11655Moexipril HCl
    CAS: 82586-52-5
    纯度: >98.00%

    A prodrug form of moexiprilat

  • GC12368 structure
    GC12368Quinapril HCl
    CAS: 82586-55-8
    纯度: >99.00%

    A prodrug form of quinaprilat

  • GC12859 structure
    GC12859Cilazapril
    CAS: 88768-40-5

    A prodrug form of cilazaprilat

  • GC13078 structure
    GC13078Imidapril HCl
    CAS: 89396-94-1
    纯度: >99.50%

    A prodrug form of imidaprilat

  • GC15166 structure
    GC15166Perindopril Erbumine
    CAS: 107133-36-8
    纯度: >99.50%

    An orally active ACE inhibitor

  • GC16192 structure
    GC16192Diminazene Aceturate
    CAS: 908-54-3
    纯度: >99.00%

    An anti-protozoal diamidine

  • GC16223 structure
    GC16223Captopril
    CAS: 62571-86-2
    纯度: >99.00%

    Captopril是一种具有口服活性的血管紧张素转化酶(ACE)抑制剂,IC 50 值为0.025μM。

  • GC16307 structure
    GC16307Lisinopril
    CAS: 76547-98-3

    An ACE inhibitor

  • GC16768 structure
    GC16768Phosphoramidon Disodium Salt
    CAS: 164204-38-0

    An inhibitor of NEP and NEP2

  • GC16871 structure
    GC16871Perindopril
    CAS: 82834-16-0

    An orally active ACE inhibitor

  • GC17034 structure
    GC17034Temocapril HCl
    CAS: 110221-44-8
    纯度: >99.50%

    A prodrug form of temocaprilat

  • GC17667 structure
    GC17667Cilazapril Monohydrate
    CAS: 92077-78-6
    纯度: >99.00%

    A prodrug form of cilazaprilat

  • GC17941 structure
    GC17941Benazepril HCl
    CAS: 86541-74-4
    纯度: >99.50% / >98.00%

    A prodrug of benazeprilat

  • GC25723 structure
    GC25723Perindopril L-Arginine
    CAS: 612548-45-5

    Perindopril L-Argininel is a prodrug that is metabolized in the liver to its active diacid metabolite perindoprilat, which is rapidly and extensively absorbed, and become one of the highest tissue angiotensin-converting enzyme (ACE) affinities among the ACE inhibitors.

  • GC30421 structure
    GC30421Enalapril D5 maleate (MK-421 (D5 maleate))
    CAS: 349554-02-5

    An internal standard for the quantification of enalapril

  • GC31354 structure
    GC31354MLN-4760
    CAS: 305335-31-3
    纯度: >99.00%

    MLN-4760是一种选择性的人血管紧张素转换酶2(ACE2;IC 50 =0.44nM)抑制剂,MLN-4760可高亲和力地结合ACE2的活性位点锌离子,模拟肽水解过程中的过渡态,从而阻断血管紧张素II向血管紧张素(1-7)的转化。