Atropine

CAT:
804-HY-B1205-01
Size:
100 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Atropine - image 1

Atropine

  • Description:

    Atropine (Tropine tropate) is a competitive muscarinic acetylcholine receptor (mAChR) antagonist with IC50 values of 0.39 and 0.71 nM for Human mAChR M4 and Chicken mAChR M4, respectively. Atropine inhibits ACh-induced relaxations in human pulmonary veins. Atropine can be used for research of anti-myopia and bradycardia[1][2][3][4].
  • Product Name Alternative:

    Tropine tropate; DL-Hyoscyamine
  • UNSPSC:

    12352005
  • Hazard Statement:

    H300, H330
  • Target:

    Endogenous Metabolite; mAChR
  • Type:

    Natural Products
  • Related Pathways:

    GPCR/G Protein; Metabolic Enzyme/Protease; Neuronal Signaling
  • Applications:

    Neuroscience-Neuromodulation
  • Field of Research:

    Neurological Disease; Cardiovascular Disease; Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/Atropine.html
  • Purity:

    99.85
  • Solubility:

    DMSO : ≥ 96.6 mg/mL|H2O : 2.9 mg/mL (ultrasonic; warming)
  • Smiles:

    O=C(O[C@@H]1C[C@@H](N2C)CC[C@@H]2C1)C(CO)C3=CC=CC=C3
  • Molecular Formula:

    C17H23NO3
  • Molecular Weight:

    289.38
  • Precautions:

    H300, H330
  • References & Citations:

    [1]McBrien NA, et, al. How does atropine exert its anti-myopia effects? Ophthalmic Physiol Opt. 2013 May;33 (3) :373-8.|[2]Morhardt JE. Heart rates, breathing rates and the effects of atropine and acetylcholine on white-footed mice (Peromyscus sp.) during daily torpor. Comp Biochem Physiol. 1970 Mar 15;33 (2) :441-57.|[3]Carr BJ, et, al. Myopia-Inhibiting Concentrations of Muscarinic Receptor Antagonists Block Activation of Alpha2A-Adrenoceptors In Vitro. Invest Ophthalmol Vis Sci. 2018 Jun 1;59 (7) :2778-2791.|[4]Walch L, et, al. Evidence for a M (1) muscarinic receptor on the endothelium of human pulmonary veins. Br J Pharmacol. 2000 May;130 (1) :73-8.
  • Shipping Conditions:

    Blue Ice
  • Storage Conditions:

    -20°C (Powder, stored under nitrogen)
  • Scientific Category:

    Natural Products
  • Clinical Information:

    Launched
  • Isoform:

    MAChR4
  • Citation 01:

    Can J Physiol Pharmacol. 2020 Oct;98 (10) :725-732.|Cardiovasc Drugs Ther. 2025 Apr 7.|Cell Metab. 2022 Dec 6;34 (12) :1999-2017.e10.|Cell Rep. 2022 Mar 8;38 (10) :110468.|Cell. 2025 Oct 24:S0092-8674 (25) 01129-8.|Eur J Pharmacol. 2024 Sep 3:176954.|Food Chem. 2022 Nov 30:395:133593.|Front Pharmacol. 2020 Jul 31;11:1038.|J Biosci. 2021:46:90.|J Ethnopharmacol. 2024 Jan 30;319 (Pt 2) :117192.|J Hazard Mater. 2024 Mar 5:465:133248.|J Hazard Mater. 2024 Sep 5:479:135690.|J Transl Med. 2025 Jan 23;23 (1) :112.|Research Square Preprint. 2022 Mar.|Research Square Print. 2023 Feb 7.|Research Square Print. December 16th, 2022.|Arch Oral Biol. 2023 Jan:145:105586.|Cell Discov. 2023 Feb 7;9 (1) :16.|Neuron. 2022 Nov 16;110 (22) :3774-3788.e7.
  • CAS Number:

    [51-55-8]