Item no. |
HY-13715-500mg |
Manufacturer |
MedChem Express
|
CASRN |
51-41-2 |
Amount |
500 mg |
Quantity options |
100 mg
10 mM/1 mL
500 mg
|
Category |
|
Type |
Inhibitors |
Specific against |
other |
Purity |
99.43 |
Formula |
C8H11NO3 |
Citations |
ACS Nano. 2022 Aug 23;16(8):12553-12568. Biochem Biophys Res Commun. 2023 Mar 24;657:108-118. bioRxiv. 2023 Oct 13. bioRxiv. 2024 July 31. bioRxiv. 2024 November 03. Cell Commun Signal. 2024 Jul 25;22(1):375. Cell Death Dis. 2020 Aug 18;11(8):644. Cell Mol Immunol. 2023 Jan 5. Cell Rep Med. 2023 May 24;101061. Eur J Pharmacol. 2022 May 12;175022. Food Science and Human Wellness. 2023 Nov;12(6);2061-2072. Gene. 2023 Aug 31;147753. Int J Mol Sci. 2022, 23(20), 12420. J Am Heart Assoc. 2019 Jan 8;8(1):e009871. J Biol Chem. 2024 Oct 23:107924. J Cancer. 2024 Sep 9;15(17):5691-5709. J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Aug 15;1092:220-227. J Ethnopharmacol. 2024 Sep 26:118860. J Therm Biol. 2024 Jul 2:123:103906. Nat Commun. 2022 Jul 25;13(1):4278. Nat Commun. 2024 May 7;15(1):3834. Neurochem Int. 2020 Dec 16;104942. Sci Rep. 2022 Jun 15;12(1):9936. SSRN. 2023 May 8. Br J Pharmacol. 2020 Aug;177(15):3389-3402. Cell Rep. 2019 Dec 3;29(10):2936-2943.e4. J Nutr Biochem. 2018 May 1;58:110-118. Leiden University. Institute of Biology Leiden (IBL) , Faculty of Science. Nature. 2024 Dec 18. Neuroscience. 2019 Mar 1;401:59-72. Research Square Preprint. 2021 Aug. Theranostics. 2022 Jun 6;12(10):4718-4733. Cardiovasc Res. 2018 Feb 1;114(2):300-311. Cell Biochem Funct. 2024 Jan 11. FASEB J. 2020 Nov;34(11):14892-14904. [1]MacGregor DA, et al. Relative efficacy and potency of beta-adrenoceptor agonists for generating cAMP in human lymphocytes. Chest. 1996 Jan;109(1):194-200. [2]Littlejohn NK, et al. Suppression of Resting Metabolism by the Angiotensin AT2 Receptor. Cell Rep. 2016 Aug 9;16(6):1548-60. [3]Brian P Ramos, et al. Adrenergic pharmacology and cognition: focus on the prefrontal cortex. Pharmacol Ther. 2007 Mar;113(3):523-36. [4]Xinyu Xu, et al. Binding pathway determines norepinephrine selectivity for the human β 1 AR over β 2 AR. Cell Res. 2021 May;31(5):569-579. [5]Xiao D, et al. "Inhibition of DNA methylation reverses norepinephrine-induced cardiac hypertrophy in rats." Cardiovascular research 101.3 (2014): 373-382. [6]Yamazaki, et al. "Norepinephrine induces the raf-1 kinase/mitogen-activated protein kinase cascade through both α1-and β-adrenoceptors." Circulation 95.5 (1997): 1260-1268. |
Smiles |
OC1=CC=C([C@@H](O)CN)C=C1O |
ECLASS 10.1 |
32160490 |
ECLASS 11.0 |
32160490 |
UNSPSC |
12000000 |
Alias |
Levarterenol, L-Noradrenaline |
Shipping condition |
Room temperature |
Available |
|
Manufacturer - Type |
Natural Products |
Manufacturer - Targets |
Adrenergic Receptor; Autophagy; Endogenous Metabolite |
Shipping Temperature |
Room Temperature |
Storage Conditions |
4°C (Powder, protect from light, stored under nitrogen) |
Molecular Weight |
169.18 |
Product Description |
Norepinephrine (Levarterenol; L-Noradrenaline) is a potent adrenergic receptor (AR) agonist. Norepinephrine activates α1, α2, β1 receptors[1][2][3][4]. |
Manufacturer - Research Area |
Endocrinology; Cardiovascular Disease; Cancer |
Solubility |
DMSO : 50 mg/mL (ultrasonic; adjust pH to 2 with HCl)|H2O : 33.33 mg/mL (ultrasonic; adjust pH to 1 with 1 M HCL) |
Manufacturer - Pathway |
Autophagy; GPCR/G Protein; Metabolic Enzyme/Protease; Neuronal Signaling |
Isoform |
Human Endogenous Metabolite; Microbial Metabolite; α adrenergic receptor; β adrenergic receptor |
Clinical information |
Launched |
Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.
All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.