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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Galantamine Hydrobromide - 10mM in Water , CAS No.1953-04-4
Disponível para encomenda
GRADE & PURITY 10mM in Water
Synonyms
Galanthamine hydrobromide|Galantamine hydrobromide|1953-04-4|Reminyl|Nivalin|Nivaline|Lycoremine hydrobromide|Jilkon hydrobromide|Razadyne|Tamilin|Galanthamine (hydrobromide)|MJ4PTD2VVW|Nivaline (pharmaceutical)|Jilcon hydrobromide|(-)-Galantamine Hydrobr
Storage
Protected from light,Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in Water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
Galanthamine hydrobromide | Galantamine hydrobromide | 1953-04-4 | Reminyl | Nivalin | Nivaline | Lycoremine hydrobromide | Jilkon hydrobromide | Razadyne | Tamilin | Galanthamine (hydrobromide) | MJ4PTD2VVW | Nivaline (pharmaceutical) | Jilcon hydrobromide | (-)-Galantamine Hydrobr
Especificações e pureza
10mM in Water
Mecanismos bioquímicos e fisiológicos
Galanthamine hydrobromide is a long-acting, centrally active acetylcholinesterase inhibitor (IC50 = 410 nM) and allosteric potentiator at neuronal nicotinic ACh receptors. Galanthamine hydrobromide prevents β-amyloid-induced apoptosis in SH-SY5Y and
Condições de armazenamento de armazenamento
Protected from light,Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores Sorrisos canónicos
CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O.Br
IUPAC Name
(1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-ol;hydrobromide
InChIKey
QORVDGQLPPAFRS-XPSHAMGMSA-N
INCHI
1S/C17H21NO3.BrH/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17;/h3-6,12,14,19H,7-10H2,1-2H3;1H/t12-,14-,17-;/m0./s1
SMILES isoméricas
CN1CC[C@@]23C=C[C@@H](C[C@@H]2OC4=C(C=CC(=C34)C1)OC)O.Br
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=40264879&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Alkaloids and derivatives Classe Amaryllidaceae alkaloids Subclass Galanthamine-type amaryllidaceae alkaloids Intermediate Tree Nodes Not available Direct Parent Galanthamine-type amaryllidaceae alkaloids Alternative Parents Benzazepines Coumarans Anisoles Azepines Aralkylamines Alkyl aryl ethers Trialkylamines Secondary alcohols Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Hydrobromides Molecular Framework Aromatic heteropolycyclic compounds Substituents Galanthamine-type amaryllidaceae alkaloid - Benzazepine - Coumaran - Anisole - Alkyl aryl ether - Azepine - Aralkylamine - Benzenoid - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Oxacycle - Ether - Organoheterocyclic compound - Azacycle - Amine - Organic nitrogen compound - Alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Hydrobromide - Aromatic heteropolycyclic compound Descrição This compound belongs to the class of organic compounds known as galanthamine-type amaryllidaceae alkaloids. These are amaryllidaceae alkaloids with a structure characterized a tetracyclic skeleton with two ortho aromatic protons in ring A. External Descriptors Not available Data sources 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.
Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Sensibilidade Light Sensitive,Hygroscopic,Heat Sensitive Rotação específica [α] -95 ° (C=1.4, H2O) Ponto de fusão (°C) 256°C Peso molecular 368.300 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 1 Exact Mass 367.078 Da Monoisotopic Mass 367.078 Da Topological Polar Surface Area 41.900 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 440.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 3 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
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