1. Metabolic Enzyme/Protease
  2. Angiotensin-converting Enzyme (ACE)
  3. Zabicipril

Zabicipril is an orally active angiotensin-converting enzyme (ACE) inhibitor. Zabicipril can be used for the study of blood pressure and peripheral arterial insufficiency.

For research use only. We do not sell to patients.

Zabicipril Chemical Structure

Zabicipril Chemical Structure

CAS No. : 83059-56-7

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Description

Zabicipril is an orally active angiotensin-converting enzyme (ACE) inhibitor. Zabicipril can be used for the study of blood pressure and peripheral arterial insufficiency[1].

In Vivo

Zabicipril (0.3, 3 mg/kg; p.o.; daily for 5-7 days) inhibits ACE in rat plasma[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Adult male Sprague-Dawley rats[1]
Dosage: 0.3, 3 mg/kg
Administration: P.o.; daily for 5-7 days
Result: Induced 50% and 65% inhibition of plasma ACE activity in the low- and high-dose group, respectively.
Molecular Weight

416.51

Formula

C23H32N2O5

CAS No.
SMILES

CCOC([C@H](CCC1=CC=CC=C1)N[C@@H](C)C(N2[C@@H](C3([H])CCC2([H])CC3)C(O)=O)=O)=O

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Zabicipril
Cat. No.:
HY-105266
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