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Methscopolamine Bromide - ≥98%, high purity , Muscarinic acetylcholine receptor M1 antagonist, CAS No.155-41-9, Muscarinic acetylcholine receptor M1 antagonist

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Methscopolamine Bromide - ≥98%, high purity , Muscarinic acetylcholine receptor M1 antagonist, CAS No.155-41-9, Muscarinic acetylcholine receptor M1 antagonist

5 Citations

COA

Grade & Purity:

≥98%

Cas Number: 155-41-9
Molecular Weight: 398.29
MDL number: MFCD00078560
PubChem CID: 5459110
PubChem SID: 504763822

In stock

Item Number

S129958

Grouped product items
SKU	Size	Availability	Price
S129958-200mg	200mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$21.90
S129958-250mg	250mg	2	$23.90
S129958-1g	1g	3	$71.90
S129958-5g	5g	2	$320.90

View related series

Cell signal transduction and Neuroscience (85) Class A GPCR (4138) quinolines (133)

Basic Description

Synonyms	UNII-292T5234DX \| (-)-scopolamine methobromide \| CAS-155-41-9 \| CCG-268630 \| Diopal \| Epoxymethamine bromide \| Methscopolamine bromide [USP] \| MFCD00078560 \| (-)-Scopolamine methyl bromide, >=98% (HPLC), powder \| 3-Oxa-9-azoniatricyclo(3.3.1.02,4)nonane,
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	(-)-Scopolamine methyl bromide is a competitive antimuscarinic agent that blocks the binding of acetylcholine at muscarinic acetylcholine receptors (mAChR M) in vitro.
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Action Type	ANTAGONIST
Mechanism of action	Muscarinic acetylcholine receptor M1 antagonist
Product Description	Methscopolamine is a muscarinic acetylcholine receptor blocker. A competitive antimuscarinic compound.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Hydroxy acids and derivatives
    - Subclass Beta hydroxy acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Hydroxy acids and derivatives
Subclass	Beta hydroxy acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Beta hydroxy acids and derivatives
Alternative Parents	Benzene and substituted derivatives Piperidines Morpholines N-alkylpyrrolidines Tetraalkylammonium salts Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Epoxides Dialkyl ethers Azacyclic compounds Organic bromide salts Organic zwitterions Hydrocarbon derivatives Amines Carbonyl compounds Primary alcohols Organic oxides
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Beta-hydroxy acid - Monocyclic benzene moiety - Morpholine - Oxazinane - Piperidine - N-alkylpyrrolidine - Benzenoid - Tetraalkylammonium salt - Pyrrolidine - Quaternary ammonium salt - Carboxylic acid ester - Carboxylic acid derivative - Dialkyl ether - Oxirane - Ether - Monocarboxylic acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Amine - Organooxygen compound - Carbonyl group - Alcohol - Primary alcohol - Organic bromide salt - Organic oxide - Organic salt - Organic zwitterion - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as beta hydroxy acids and derivatives. These are compounds containing a carboxylic acid substituted with a hydroxyl group on the C3 carbon atom.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	504763822
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504763822
IUPAC Name	[(1R,2R,4S,5S)-9,9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.02,4]nonan-7-yl] (2S)-3-hydroxy-2-phenylpropanoate;bromide
INCHI	InChI=1S/C18H24NO4.BrH/c1-19(2)14-8-12(9-15(19)17-16(14)23-17)22-18(21)13(10-20)11-6-4-3-5-7-11;/h3-7,12-17,20H,8-10H2,1-2H3;1H/q+1;/p-1/t12?,13-,14-,15+,16-,17+;/m1./s1
InChIKey	CXYRUNPLKGGUJF-OZVSTBQFSA-M
Smiles	C[N+]1(C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4)C.[Br-]
Isomeric SMILES	C[N+]1([C@@H]2CC(C[C@H]1[C@H]3[C@@H]2O3)OC(=O)[C@H](CO)C4=CC=CC=C4)C.[Br-]
PubChem CID	5459110
Molecular Weight	398.29

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot Number	Certificate Type	Date	Item
D23061270	Certificate of Analysis	Jan 10, 2025	S129958
G2215433	Certificate of Analysis	Apr 07, 2024	S129958
G2215434	Certificate of Analysis	Apr 07, 2024	S129958
E2413098	Certificate of Analysis	Apr 07, 2024	S129958
J2112303	Certificate of Analysis	Jul 10, 2023	S129958
J2112374	Certificate of Analysis	Jul 10, 2023	S129958

Chemical and Physical Properties

Solubility	Soluble in water (50 mg/ml).
Specific Rotation[α]	-24°C
Molecular Weight	398.300 g/mol
XLogP3
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	5
Exact Mass	397.089 Da
Monoisotopic Mass	397.089 Da
Topological Polar Surface Area	59.100 Å²
Heavy Atom Count	24
Formal Charge	0
Complexity	454.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	5
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	2

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Song Changgeng, Zhao Yan, Zhang Jiajia, Dong Ziyi, Kang Xin, Pan Yuqi, Du Jinle, Gao Yiting, Zhang Haifeng, Xi Ye, Ding Hui, Kuang Fang, Wang Wenting, Luo Ceng, Zhang Zhengping, Zhao Qinpeng, Yang Jiazhou, Jiang Wen, Wu Shengxi, Gao Fang. (2023) Spatial Distribution of Parvalbumin-Positive Fibers in the Mouse Brain and Their Alterations in Mouse Models of Temporal Lobe Epilepsy and Parkinson’s Disease. Neuroscience Bulletin, (1-20).
2. Song Changgeng, Zhao Jingjing, Hao Jianmin, Mi Dan, Zhang Jiajia, Liu Yingying, Wu Shengxi, Gao Fang, Jiang Wen. (2023) Aminoprocalcitonin protects against hippocampal neuronal death via preserving oxidative phosphorylation in refractory status epilepticus. Cell Death Discovery, 9 (1): (1-18).
3. Fankai Gao, Rui Chen, Shuo Li, An Li, Bo Bai, Rulin Mi, Guofang Xue. (2023) (+)-Borneol exerts neuroprotective effects via suppressing the NF-κB pathway in the pilocarpine-induced epileptogenesis rat model. BRAIN RESEARCH, 1810 (148382).
4. Huijie Huangfu, Xugeng Guo, Ning Li, Ye Xiong, Yafei Huang, Jinglai Zhang, Li Wang. (2023) A smart composite coating with self-reporting and self-healing functions to enhance corrosion protection for magnesium alloys. PROGRESS IN ORGANIC COATINGS, 181 (107598).
5. Dai Jie, Shen Hai-lin, Li Jia, Zhou Yong, Dong Zheng-xie, Zhu Xiang-yang. (2024) Gastrodin Attenuates Neuroinflammation and Injury in Young Rats with LiCl/Pilocarpine-Induced Status Epilepticus. BIOCHEMICAL GENETICS, (1-16).

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