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captopril

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Captopril
T146262571-86-2
Captopril (SA333) is a potent and specific inhibitor of peptidyl-dipeptidase A. It blocks the conversion of angiotensin I to angiotensin II, a vasoconstrictor and important regulator of arterial blood pressure.
  • $40
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TargetMol | Citations Cited
Captopril disulfide
T2051264806-05-9
Captopril disulfide, a metabolite of Captopril, is a new antihypertensive agent.
  • $296
35 days
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Captopril hydrochloride
T60383198342-23-3
Captopril (SQ 14225) hydrochloride is an antihypertensive agent that is a thiol-containing competitive, orally active angiotensin-converting enzyme (ACE) inhibitor with IC 50 of 0.025 μM and has been widely used for research of hypertension and congestive heart failure. Captopril hydrochloride is also a New Delhi metallo-β-lactamase-1 (NDM-1) inhibitor with an IC 50 of 7.9 μM [1] [2] [3].
  • $2,140
1-2 weeks
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Captopril EP Impurity E
T3988523500-15-4
Captopril EP Impurity E is an impurity of Captopril. Captopril, also known as SQ-14534, is an orally active angiotensin-converting enzyme (ACE) inhibitor that contains a thiol group. It has antihypertensive properties and competes with ACE with an inhibitor constant (IC 50 ) of 0.025 μM.
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Captopril EP Impurity D
T6751156970-78-6
Captopril EP Impurity D is a useful organic compound for research related to life sciences. The catalog number is T67511 and the CAS number is 56970-78-6.
    7-10 days
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    Captopril EP Impurity B
    T7410980629-35-2
    Captopril EP Impurity B, a degradation product of Captopril (SQ-14534), serves as a thiol-containing, competitive inhibitor of the angiotensin-converting enzyme (ACE), demonstrating oral activity and potent antihypertensive effects with an IC50 value of 0.025 μM [1] [2] [3].
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    Moveltipril
    T2583285856-54-8In house
    Moveltipril (Moveltipril calcium) is a potent angiotensin-converting enzyme (ACE) inhibitor.Moveltipril is converted to captopril in the body for action.
    • $83
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    1,4-Anthraquinone
    TN2496635-12-1
    1,4-Anthraquinone is an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro.1,4-
    • $29
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