GLPBio

Ataciguat

Catalog No.: GC11361Purity:>98.00%Synonyms: HMR 1766
Ataciguat (HMR-1766) は、一酸化窒素非依存性可溶性グアニル酸シクラーゼ (sGC) 活性化剤です。

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。


Ataciguat
Cas No.: 254877-67-3
10mM (in 1mL DMSO)In Stock
$80.00
1
1mgIn Stock
$28.00
1
5mgIn Stock
$63.00
1
10mgIn Stock
$101.00
1
25mgIn Stock
$202.00
1
50mgIn Stock
$309.00
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
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    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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    Science
    387(6734) (2025)
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    35, 97–116 (2025)
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    31, 1291–1307 (2021)

製品説明 (Description)

Ataciguat is a nitric oxide-independent soluble guanylate cyclase (sGC) activator. Ataciguat activates the oxidized heme iron redox form of sGC to stimulate cGMP production. Ataciguat can be used in research related to heart failure and aortic valve stenosis[1-4].

In vitro, Ataciguat (0.1–10μM) was used to treat HUVEC cells for 30 minutes. Ataciguat significantly increased NO production in the cells[5]. Rat aortic smooth muscle cells were pretreated with H₂O₂ (500μM) for 1 hour, followed by treatment with Ataciguat (10μM) for 15 minutes. Ataciguat significantly increased cGMP production in the cells[6].

In vivo, Ataciguat (10mg/kg; twice daily) was administered by gavage to adult male Wistar rats with chronic myocardial infarction induced by coronary ligation for 10 weeks. Ataciguat significantly improved vascular function and reduced platelet activation[7]. Ataciguat (10mg/kg; once daily) was subcutaneously injected into C57Bl/6J mice with pulmonary arterial hypertension induced by chronic hypoxia for 14 days (from day 21 to day 35 of hypoxia). Ataciguat significantly reduced pulmonary arterial hypertension and right ventricular hypertrophy[8].

References:
[1] Schindler U, Strobel H, Schönafinger K, et al. Biochemistry and pharmacology of novel anthranilic acid derivatives activating heme-oxidized soluble guanylyl cyclase. Mol Pharmacol. 2006 Apr;69(4):1260-8.
[2] Çakmak E, Yönem Ö, Saraç B, et al. Comparative Relaxant Effects of Ataciguat and Zaprinast on Sheep Sphincter of Oddi. Balkan Med J. 2016 Jul;33(4):453-7.
[3] Zhang B, Enriquez-Sarano M, Schaff HV, et al. Reactivation of Oxidized Soluble Guanylate Cyclase as a Novel Treatment Strategy to Slow Progression of Calcific Aortic Valve Stenosis: Preclinical and Randomized Clinical Trials to Assess Safety and Efficacy. Circulation. 2025 Apr;151(13):913-930.
[4] Fraccarollo D, Galuppo P, Motschenbacher S, et al. Soluble guanylyl cyclase activation improves progressive cardiac remodeling and failure after myocardial infarction. Cardioprotection over ACE inhibition. Basic Res Cardiol. 2014 Jul;109(4):421.
[5] Martinelli AM, Rodrigues CNDS, Moraes TF, et al. In Endothelial Cells, the Activation or Stimulation of Soluble Guanylyl Cyclase Induces the Nitric Oxide Production by a Mechanism Dependent of Nitric Oxide Synthase Activation. J Pharm Pharm Sci. 2018;21(1):38-45.
[6] Zhou Z, Pyriochou A, Kotanidou A, et al. Soluble guanylyl cyclase activation by HMR-1766 (ataciguat) in cells exposed to oxidative stress. Am J Physiol Heart Circ Physiol. 2008 Oct;295(4):H1763-71.
[7] Schäfer A, Fraccarollo D, Werner L, et al. Guanylyl cyclase activator ataciguat improves vascular function and reduces platelet activation in heart failure. Pharmacol Res. 2010 Nov;62(5):432-8.
[8] Weissmann N, Hackemack S, Dahal BK, et al. The soluble guanylate cyclase activator HMR1766 reverses hypoxia-induced experimental pulmonary hypertension in mice. Am J Physiol Lung Cell Mol Physiol. 2009 Oct;297(4):L658-65.

実験プロトコル (Protocol)

Cell experiment [1]:

Cell lines

Rat aortic smooth muscle cells (RASMCs) and COS7 cells

Preparation Method

RASMCs were pretreated with H₂O₂ (500μM) for 1 hour, then incubated with Ataciguat in the presence of IBMX (1mM) for 15 minutes.

Reaction Conditions

10μM; 15 minutes

Applications

Ataciguat significantly increased cGMP production in cells exposed to oxidative stress. Ataciguat was more effective in stimulating heme-free soluble guanylyl cyclase (sGC) compared to the wild-type enzyme. Exposure of cells to Ataciguat did not lead to the development of tolerance.

Animal experiment [2]:

Animal models

Male Wistar rats

Preparation Method

Chronic myocardial infarction was induced by coronary ligation in male Wistar rats. Animals were treated with Ataciguat (10mg/kg/twice; daily by gavage) starting from day 10 after surgery for 10 weeks.

Dosage form

10mg/kg; oral gavage; twice daily for 10 weeks

Applications

Ataciguat improved endothelium-dependent vasorelaxation and normalized vascular sensitivity to exogenous NO. Ataciguat reduced aortic superoxide production and increased in vivo platelet VASP phosphorylation. Ataciguat decreased platelet P-selectin surface-expression and attenuated ADP-induced platelet aggregation.

References:
[1] Zhou Z, Pyriochou A, Kotanidou A, et al. Soluble guanylyl cyclase activation by HMR-1766 (ataciguat) in cells exposed to oxidative stress. Am J Physiol Heart Circ Physiol. 2008 Oct;295(4):H1763-71.
[2] Schäfer A, Fraccarollo D, Werner L, et al. Guanylyl cyclase activator ataciguat improves vascular function and reduces platelet activation in heart failure. Pharmacol Res. 2010 Nov;62(5):432-8.

製品資料 (Product Documents)

Purity:>98.00%Appearance:A solid

化学的性質 (Chemical Properties)

CAS番号
254877-67-3
同義語
HMR 1766
化学名
5-chloro-2-[[(5-chloro-2-thienyl)sulfonyl]amino]-N-[4-(4-morpholinylsulfonyl)phenyl]-benzamide
SMILES
O=S(N1CCOCC1)(C2=CC=C(NC(C3=CC(Cl)=CC=C3NS(C4=CC=C(Cl)S4)(=O)=O)=O)C=C2)=O
分子式
C21H19Cl2N3O6S3
分子量
576.5
溶解性
≤1mg/ml in dimethyl formamide
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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