GLPBio

Perindopril

Catalog No.: GC16871Purity:>98%
Perindopril (S-9490) هو مثبط طويل المفعول للإنزيم المحول للأنجيوتنسين يستخدم لعلاج ارتفاع ضغط الدم أو قصور القلب أو مرض الشريان التاجي المستقر

المنتجات مخصصة للاستخدام البحثي فقط، وليست للاستخدام البشري. نحن لا نبيع للمرضى.


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

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    Nature
    641, 529–536 (2025)
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    Nature
    628, 630–638 (2024)
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    Nature
    632, 686–694 (2024)
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    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)
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    Science
    388(6745) (2025)
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    387(6739) (2025)
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    387(6734) (2025)
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    Cell Research
    35, 97–116 (2025)
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    31, 1291–1307 (2021)

الوصف (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.

البروتوكول (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.

الخصائص الكيميائية (Chemical Properties)

رقم CAS
82834-16-0
الاسم الكيميائي
(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
الصيغة الجزيئية
C19H32N2O5
الوزن الجزيئي
368.47
الذوبانية
Ethanol: 25 mg/ml,PBS (pH 7.2): 10 mg/ml
التخزين
Store at -20°C
إرشادات عامة
اختر مذيبًا مناسبًا وفقًا لبيانات ذوبانية المنتج. بعد التحضير، قسّم المحلول المخزون إلى أجزاء لتجنب دورات التجميد والذوبان المتكررة.
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
شروط الشحن
تُشحن عينات التقييم مع عبوات تبريد. وتُشحن الأحجام الأخرى المتاحة في درجة حرارة الغرفة، أو مع عبوات تبريد عند الطلب.

الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية

g/mol

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