GLPBio

Perindopril

Catalog No.: GC16871Purity:>98%
Perindopril (S-9490) es un inhibidor de la ECA de acciÓn prolongada que se usa para tratar la presiÓn arterial alta, la insuficiencia cardÍaca o la enfermedad arterial coronaria estable.

Los productos son exclusivamente para uso en investigación. No aptos para uso humano. No vendemos a pacientes.


Perindopril
Cas No.: 82834-16-0
10mM (in 1mL DMSO)In Stock
$30.00
1
25mgIn Stock
$27.00
1
50mgIn Stock
$45.00
1
100mgIn Stock
$72.00
1

Citas (Citations)

Actualmente no hay citas disponibles para este producto. A continuación se muestran publicaciones seleccionadas que citan productos GlpBio.
  • Nature cover
    Nature
    641, 529–536 (2025)
  • Nature cover
    Nature
    628, 630–638 (2024)
  • Nature cover
    Nature
    632, 686–694 (2024)
  • Nature cover
    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
  • Science cover
    Science
    387(6739) (2025)
  • Science cover
    Science
    387(6734) (2025)
  • Cell Research cover
    Cell Research
    35, 97–116 (2025)
  • Cell Research cover
    Cell Research
    34, 683–706 (2024)
  • Cell Research cover
    Cell Research
    33, 273–287 (2023)
  • Cell Research cover
    Cell Research
    33, 546–561 (2023)
  • Cell Research cover
    Cell Research
    33, 904–922 (2023)
  • Cell Research cover
    Cell Research
    31, 1291–1307 (2021)

Descripción (Description)

Perindopril is an angiotensin-converting enzyme (ACE) inhibitor. Perindopril lowers blood pressure and cardiac load by inhibiting the conversion of angiotensin I to angiotensin II and reducing the degradation of bradykinin. Perindopril is used in the treatment of hypertension and heart failure[1-4].

In vitro, differentiated SH-SY5Y cells were pretreated with Perindopril (1-10μg/mL) for 24 hours, followed by stimulation with LPS (20μg/mL) for 1 hour. Perindopril significantly increased cell viability but showed no significant effects on acetylcholine (ACh) levels or the expression of pro-inflammatory factors (TNF-α, IL-1β, NFκB)[5]. Perindopril (100μM) treated THP-1 macrophages for 24 hours. Perindopril inhibited SARS-CoV-2 Spike protein (100nM)-induced apoptosis, reactive oxygen species generation, and MHC-II expression[6].

In vivo, Swiss mice were orally administered Perindopril (1mg/kg; single dose) 1 hour before establishing chemical, thermal, and mechanical pain models. Perindopril significantly reduced the number of writhes in mice, delayed reaction times in the tail clip test, and increased latency in the hot plate test[7]. Starting 1 hour before a single intraperitoneal injection of cisplatin (10mg/kg), Swiss mice were orally administered Perindopril (2mg/kg; once daily) for 5 consecutive days. Perindopril significantly improved cisplatin-induced renal histological changes, levels of inflammatory factors (TNF-α, IL-6, IL-10), and expression of apoptosis-related proteins (Bax, Bcl2, caspase-3)[8].

References:
[1] Alfakih K, Hall AS. Perindopril. Expert Opin Pharmacother. 2006 Jan;7(1):63-71.
[2] Lababidi JM, Kabil MF, Azzazy HME. Perindopril: A comprehensive profile. Profiles Drug Subst Excip Relat Methodol. 2026;51:211-252.
[3] Ghiadoni L. Perindopril for the treatment of hypertension. Expert Opin Pharmacother. 2011 Jul;12(10):1633-42.
[4] Simpson D, Noble S, Goa KL. Perindopril: in congestive heart failure. Drugs. 2002;62(9):1367-77.
[5] Şen S, Hacıosmanoğlu E. Comparing the Neuroprotective Effects of Telmisartan, Perindopril, and Nebivolol Against Lipopolysaccharide-Induced Injury in Neuron-Like Cells. Cureus. 2022 Jul 29;14(7):e27429.
[6] Barhoumi T, Alghanem B, Shaibah H, et al. SARS-CoV-2 Coronavirus Spike Protein-Induced Apoptosis, Inflammatory, and Oxidative Stress Responses in THP-1-Like-Macrophages: Potential Role of Angiotensin-Converting Enzyme Inhibitor (Perindopril). Front Immunol. 2021 Sep 20;12:728896.
[7] Suresha RN, Amoghimath S, Vaibhavi PS, et al. Evaluation of analgesic activity of perindopril in albino mice. J Adv Pharm Technol Res. 2014 Jul;5(3):129-33.
[8] Aljuhani N, Ismail RS, El-Awady MS, et al. Modulatory effects of perindopril on cisplatin-induced nephrotoxicity in mice: Implication of inflammatory cytokines and caspase-3 mediated apoptosis. Acta Pharm. 2020 Dec 1;70(4):515-525.

Protocolo (Protocol)

Cell experiment [1]:

Cell lines

Differentiated SH-SY5Y cell line (human neuroblastoma cell line differentiated to neuronal phenotype)

Preparation Method

Cells were differentiated with retinoic acid for one week in serum-free neurobasal medium. Cells were pre-treated with LPS (20μg/mL) for one hour, then exposed to Perindopril at concentrations of 1-10μg/mL for 24 hours.

Reaction Conditions

1-10μg/mL; 24 hours

Applications

Perindopril significantly increased cell viability against LPS-induced injury at all doses. Perindopril showed no statistically significant changes in acetylcholine (ACh) levels after LPS-induced injury. No significant changes in TNF-α, IL-1β, and NFκB expressions were detected with the administration of Perindopril.

Animal experiment [2]:

Animal models

Swiss albino mice (Swiss strain)

Preparation Method

The mcie received Perindopril (1mg/kg) per orally. Perindopril were administered 2h before the experiment. Analgesic activity was evaluated using Eddy's hot plate (thermal pain), acetic acid-induced writhing (chemical pain), and tail clip (mechanical pain) methods.

Dosage form

1mg/kg; orally; single dose administered 2h before testing

Applications

Perindopril significantly decreased the number of writhes in the acetic acid-induced writhing test, delayed the reaction time in the tail clip method, and increased the latency period in the Eddy's hot plate method compared to the control group, demonstrating analgesic activity in thermal, chemical, and mechanical pain models.

References:
[1] Şen S, Hacıosmanoğlu E. Comparing the Neuroprotective Effects of Telmisartan, Perindopril, and Nebivolol Against Lipopolysaccharide-Induced Injury in Neuron-Like Cells. Cureus. 2022 Jul 29;14(7):e27429.
[2] Suresha RN, Amoghimath S, Vaibhavi PS, et al. Evaluation of analgesic activity of perindopril in albino mice. J Adv Pharm Technol Res. 2014 Jul;5(3):129-33.

Propiedades químicas (Chemical Properties)

N.º CAS
82834-16-0
Nombre químico
(2S,3aS,7aS)-1-[(2S)-2-[[(2S)-1-ethoxy-1-oxopentan-2-yl]amino]propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylic acid
SMILES
CCCC(C(=O)OCC)NC(C)C(=O)N1C2CCCCC2CC1C(=O)O
Fórmula molecular
C19H32N2O5
Peso molecular
368.47
Solubilidad
Ethanol: 25 mg/ml,PBS (pH 7.2): 10 mg/ml
Almacenamiento
Store at -20°C
Consejos generales
Seleccione un disolvente adecuado según los datos de solubilidad del producto. Una vez preparada, divida la solución madre en alícuotas para evitar ciclos repetidos de congelación y descongelación.
Utilice las soluciones madre en un plazo de 6 meses si se conservan a -80°C, o de 1 mes si se conservan a -20°C.
Para mejorar la solubilidad, caliente el tubo a 37°C y soníquelo durante un periodo adecuado.
Condiciones de envío
Las muestras de evaluación se envían con acumuladores de frío. Los demás tamaños se envían a temperatura ambiente o, previa solicitud, con acumuladores de frío.

Calculadoras (Calculators)Molaridad / Dilución / Peso molecular / Conversión de unidades / Formulación in vivo / Solubilidad

g/mol

Reviews

Review for Perindopril

Rating: 5
  • 5 Star100%
  • 4 Star0%
  • 3 Star0%
  • 2 Star0%
  • 1 Star0%