GLPBio

Nadolol

Catalog No.: GC39740Purity:>98.00%
Nadolol (SQ-11725) هو مانع لمستقبلات بيتا الأدرينالية غير انتقائي ونشط عن طريق الفم وهو عبارة عن ركيزة من الأنيون العضوي الذي ينقل بولي ببتيد 1A2 (OATP1A2)

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


Nadolol
Cas No.: 42200-33-9
10mM (in 1mL DMSO)In Stock
$40.00
1
50mgIn Stock
$75.00
1
100mgIn Stock
$120.00
1
250mgIn Stock
$206.00
1
500mgIn Stock
$350.00
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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    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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    33, 273–287 (2023)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

الوصف (Description)

Nadolol is a non-selective and orally active beta-adrenergic antagonist with antihypertensive and antiarrhythmic activities [1]. Nadolol can inhibit the calmodulin-activated Ca2+-ATPase of human erythrocyte membranes [2]. Nadolol has been widely used to reduce heart rate at rest and during exercise and to reduce plasma renin activity[3].

In vitro, Nadolol treatment (10µM) for 24 hours significantly increased Gαs protein levels and enhanced basal cAMP levels in β2AR-expressing HEK 293 cells[4]. Treatment with 250µM Nadolol for 48h induced apoptosis and decreased mitochondrial membrane potential in A549 cells[5].

In vivo, Nadolol treatment via intraperitoneal injection at a single dose of 20mg/kg significantly reduced the number and area of lung metastases in a B16F10 cell-xenograft mouse model under acute social stress during 15 days[6]. A single dose of 5mg/kg Nadolol was injected intraperitoneally at 1h after reperfusion, which significantly reversed the increases in neurological deficit score and infarct volume in the ischemic stroke rats[7].

References:
[1] Kalsoom S, Zamir A, Rehman A U, et al. Clinical pharmacokinetics of nadolol: A systematic review[J]. Journal of Clinical Pharmacy and Therapeutics, 2022, 47(10): 1506-1516.
[2] Meltzer H L, Kassir S. Inhibition of calmodulin-activated Ca2+-ATPase by propranolol and nadolol[J]. Biochimica et Biophysica Acta (BBA)-General Subjects, 1983, 755(3): 452-456.
[3] Heel R C, Brogden R N, Pakes G E, et al. Nadolol: a review of its pharmacological properties and therapeutic efficacy in hypertension and angina pectoris[J]. Drugs, 1980, 20(1): 1-23.
[4] Peng H, Bond R A, Knoll B J. The effects of acute and chronic nadolol treatment on β2AR signaling in HEK293 cells[J]. Naunyn-Schmiedeberg's archives of pharmacology, 2011, 383(2): 209-216.
[5] Kavakcıoğlu Yardımcı B, Geyikoglu F, Aysin F, et al. The cytotoxic and apoptotic effects of beta-blockers with different selectivity on cancerous and healthy lung cell lines[J]. Molecular Biology Reports, 2021, 48(5): 4009-4019.
[6] Vegas O, Garmendia L, Arregi A, et al. Effects of antalarmin and nadolol on the relationship between social stress and pulmonary metastasis development in male OF1 mice[J]. Behavioural brain research, 2009, 205(1): 200-206.
[7] Yang X Y, Zhu W J, Chen D, et al. Nadolol Attenuates Brain Cell Ferroptosis in Ischemic Stroke Rats by Targeting the HOIL-1/IRP2 Pathway[J]. CNS & Neurological Disorders-Drug Targets, 2025, 24(5): 397-408.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

A549 cells

Preparation Method

A549 cells were cultured in DMEM/F12 medium supplemented with 10% fetal bovine serum (FBS) and antibiotics (penicillin 100U/ml, streptomycin 0.1mg/ml) under normal conditions (5% CO2 with 95% humidified air). A549 cells (1×104 per well) were inoculated in a 96-well cell culture plate and incubated at 37°C with 5% CO2 for 24h. Then, the cells were treated with different concentrations of Nadolol (5, 10, 25, 50, 100, 150, 200, and 250µM) for 48h, respectively, and cell viability was measured.

Reaction Conditions

5, 10, 25, 50, 100, 150, 200, and 250µM; 48h

Applications

Nadolol treatment reduced the cell viability of A549 cells in a dose-dependent manner.
Animal experiment [2]:

Animal models

Male Sprague-Dawley (SD) rats

Preparation Method

Male Sprague-Dawley (SD) rats (250-300g) were housed in groups of 3-5 rats per cage with free access to food and water ad libitum. The 12-h light/dark cycles were maintained throughout the duration of animal housing, with light periods beginning consistently at 7:00 am. Before surgery, the rats were fasted overnight but were free to drink tap water. The ischemic stroke rat model was constructed by Middle Cerebral Artery Occlusion (MCAO). Rats were randomly distributed into four groups (n=12 per group): (1) the sham group, (2) the stroke group, (3) the stroke+Nadolol group, rats received Nadolol (5mg/kg; i.p.) at 1h after reperfusion, and (4) the stroke+vehicle group, rats received DMSO (i.p.) at 1h after reperfusion. Following the end of reperfusion, an assessment of the neurological deficit score was first conducted, and then the rats were executed under anesthesia. The brain tissues were preserved for infarct volume measurement.

Dosage form

5mg/kg for once; i.p.

Applications

Nadolol treatment reversed the increases in neurological deficit score and infarct volume in the ischemic stroke rats.

References:
[1] Kavakcıoğlu Yardımcı B, Geyikoglu F, Aysin F, et al. The cytotoxic and apoptotic effects of beta-blockers with different selectivity on cancerous and healthy lung cell lines[J]. Molecular Biology Reports, 2021, 48(5): 4009-4019.
[2] Yang X Y, Zhu W J, Chen D, et al. Nadolol Attenuates Brain Cell Ferroptosis in Ischemic Stroke Rats by Targeting the HOIL-1/IRP2 Pathway[J]. CNS & Neurological Disorders-Drug Targets, 2025, 24(5): 397-408.

وثائق المنتج (Product Documents)

Purity:>98.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
42200-33-9
SMILES
OC1CC2=C(C(OCC(O)CNC(C)(C)C)=CC=C2)CC1O
الصيغة الجزيئية
C17H27NO4
الوزن الجزيئي
309.4
الذوبانية
Methanol: 250 mg/mL (808.02 mM)
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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