GLPBio

Perindopril

Catalog No.: GC16871Purity:>98%
ペリンドプリル (S-9490) は長時間作用型の ACE 阻害剤で、高血圧、心不全、または安定した冠動脈疾患の治療に使用されます。

製品は研究用途にのみ使用できます。人体には使用できません。患者への販売は行っておりません。


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

引用文献 (Citations)

現在、この製品の引用文献はありません。以下はGlpBio製品を引用した代表的な文献です。
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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)
  • Science cover
    Science
    388(6745) (2025)
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    Science
    387(6739) (2025)
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    Science
    387(6734) (2025)
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    Cell Research
    35, 97–116 (2025)
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    34, 683–706 (2024)
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    31, 1291–1307 (2021)

製品説明 (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.

実験プロトコル (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.

化学的性質 (Chemical Properties)

CAS番号
82834-16-0
化学名
(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
分子式
C19H32N2O5
分子量
368.47
溶解性
Ethanol: 25 mg/ml,PBS (pH 7.2): 10 mg/ml
保存条件
Store at -20°C
一般的な注意事項
製品の溶解性データに基づいて適切な溶媒を選択してください。調製後は、凍結融解の繰り返しを避けるため、ストック溶液を小分けしてください。
ストック溶液は、-80°Cで保存する場合は6か月以内、-20°Cで保存する場合は1か月以内に使用してください。
溶解性を高めるには、チューブを37°Cに温め、適切な時間超音波処理してください。
配送条件
評価用サンプルは保冷剤とともに発送します。その他の容量は室温で発送し、ご要望に応じて保冷剤を同梱します。

計算ツール (Calculators)モル濃度 / 希釈 / 分子量 / 単位変換 / in vivo製剤 / 溶解度

g/mol

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