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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag für Lagerartikel Zinterol hydrochloride - ≥98%(HPLC) , CAS No.38241-28-0
Synonyms
Zinterol HCl|Zinterol hydrochloride [USAN]|Zinterol hydrochloride (USAN)|Methanesulfonanilide, 5'-(2-((alpha,alpha-dimethylphenethyl)amino)-1-hydroxyethyl)-2'-hydroxy-, monohydrochloride|Zinterol (hydrochloride)|(+-)-Zinterol hydrochloride|ZINTEROL HYDROCHLORIDE|Methanesulfonamide, N-(5-(2-((1,1-dimethyl-2-phenylethyl)amino)-1-hydroxyethyl)-2-hydroxyphenyl)-, monohydrochloride, (+-)-|N-[5-[2-[(1,1-Dimethyl-2-phenylethyl)amino]-1-hydroxyethyl]-2-hydroxyphenyl]methanesulphonamide hydrochloride|5'-(2-((alpha,alpha-Dimethylphenethyl)amino)-1-hydroxyethyl)-2'-hydroxymethanesulfonanilide monohydrochloride|MJ 9184|N-(2-Hydroxy-5-{1-hydroxy-2-[(2-methyl-1-phenylpropan-2-yl)amino]ethyl}phenyl)methanesulfonamide--hydrogen chloride (1/1)|N-[2-hydroxy-5-[1-hydroxy-2-[(2-methyl-1-phenylpropan-2-yl)amino]ethyl]phenyl]methanesulfonamide;hydrochloride|5'-[2-[(.alpha.,.alpha.-Dimethylphenethyl)amino]-1-hydroxyethyl]-2'-hydroxymethanesulfonanilide monohydrochloride|5'-(2-((.ALPHA.,.ALPHA.-DIMETHYLPHENETHYL)AMINO)-1-HYDROXYETHYL)-2'-HYDROXYMETHANESULFONANILIDE MONOHYDROCHLORIDE|Methanesulfonamide,1-dimethyl-2-phenylethyl)amino]-1-hydroxyethyl]-2-hydroxyphenyl]-, monohydrochloride|Methanesulfonamide, N-(5-(2-((1,1-dimethyl-2-phenylethyl)amino)-1-hydroxyethyl)-2-hydroxyphenyl)-, monohydrochloride
Spezifikationen Synonyme
Zinterol HCl | Zinterol hydrochloride [USAN] | Zinterol hydrochloride (USAN) | Methanesulfonanilide, 5'-(2-((alpha,alpha-dimethylphenethyl)amino)-1-hydroxyethyl)-2'-hydroxy-, monohydrochloride | Zinterol (hydrochloride) | (+-)-Zinterol hydrochloride | ZINTEROL HYDROCHLORIDE | Methanesulfonamide, N-(5-(2-((1,1-dimethyl-2-phenylethyl)amino) Show more
Spezifikationen & Reinheit
≥98%(HPLC)
Biochemische und physiologische Mechanismen
Potent and selectiveβ2-adrenoceptor agonist (pKBvalues are 8.3 and < 5.7 forβ2andβ1receptors respectively, as measured in human artery).
Verschickt in
Wet ice
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Namen und Kennungen Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504753563
Kanonisches Lächeln
CC(C)(CC1=CC=CC=C1)NCC(C2=CC(=C(C=C2)O)NS(=O)(=O)C)O.Cl
IUPAC Name
N-[2-hydroxy-5-[1-hydroxy-2-[(2-methyl-1-phenylpropan-2-yl)amino]ethyl]phenyl]methanesulfonamide;hydrochloride
InChIKey
LVNUBJDWJFOMKH-UHFFFAOYSA-N
INCHI
1S/C19H26N2O4S.ClH/c1-19(2,12-14-7-5-4-6-8-14)20-13-18(23)15-9-10-17(22)16(11-15)21-26(3,24)25;/h4-11,18,20-23H,12-13H2,1-3H3;1H
Isomere SMILES
CC(C)(CC1=CC=CC=C1)NCC(C2=CC(=C(C=C2)O)NS(=O)(=O)C)O.Cl
Erweiterte Daten Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Klasse Benzene and substituted derivatives Subclass Phenethylamines Intermediate Tree Nodes Not available Direct Parent Amphetamines and derivatives Alternative Parents Sulfanilides Phenylpropanes Aralkylamines 1-hydroxy-2-unsubstituted benzenoids Organosulfonamides Organic sulfonamides Aminosulfonyl compounds Secondary alcohols 1,2-aminoalcohols Dialkylamines Organopnictogen compounds Organic oxides Hydrochlorides Hydrocarbon derivatives Aromatic alcohols Molecular Framework Aromatic homomonocyclic compounds Substituents Amphetamine or derivatives - Sulfanilide - Phenylpropane - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aralkylamine - Organic sulfonic acid amide - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Secondary alcohol - 1,2-aminoalcohol - Secondary aliphatic amine - Secondary amine - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrochloride - Amine - Aromatic alcohol - Aromatic homomonocyclic compound Beschreibung This compound belongs to the class of organic compounds known as amphetamines and derivatives. These are organic compounds containing or derived from 1-phenylpropan-2-amine. 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.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Löslichkeit Solvent:water, Max Conc. mg/mL: 2.07, Max Conc. mM: 5; Solvent:DMSO, Max Conc. mg/mL: 41.49, Max Conc. mM: 100 Molekulargewicht 414.900 g/mol XLogP3 Hydrogen Bond Donor Count 5 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 8 Exact Mass 414.138 Da Monoisotopic Mass 414.138 Da Topological Polar Surface Area 107.000 Ų Heavy Atom Count 27 Formal Charge 0 Complexity 526.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 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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