Moxisylyte hydrochloride - 10mM in DMSO , CAS No.964-52-3

CAS: 964-52-3 Cat. No.: M427167 Summenformel: C₁₆H₂₆ClNO₃ Molekulargewicht: 315.84 EG-Nummer: 213-519-4

GRADE & PURITY 10mM in DMSO

Synonyms

Carvacrol, acetate (ester), hydrochloride | SCHEMBL15159483 | SMR000058476 | AKOS005203374 | WK2KZM9V6X | SCHEMBL317080 | Pipotiazin Retard | DTXSID70867309 | NCGC00261452-01 | s5666 | CHEBI:31868 | HMS1704O01 | 1-N-(L(-)-gamma-Amino-alpha-hydroxybutyryl)

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

Product description

Moxisylyte (hydrochloride) is (alpha 1-blocker) antagonist, it can vasodilates cerebral vessels without reducing blood pressure. It is also used locally in the eye to reverse the mydriasis caused by phenylephrine and other sympathomimetic agents.

Specifications

Synonyme

Carvacrol, acetate (ester), hydrochloride | SCHEMBL15159483 | SMR000058476 | AKOS005203374 | WK2KZM9V6X | SCHEMBL317080 | Pipotiazin Retard | DTXSID70867309 | NCGC00261452-01 | s5666 | CHEBI:31868 | HMS1704O01 | 1-N-(L(-)-gamma-Amino-alpha-hydroxybutyryl)

Spezifikationen & Reinheit

10mM in DMSO

Storage

Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Aktionsart

ANTAGONIST

Namen und Kennungen

Pubchem Sid

528765657

Kanonisches Lächeln

CC1=CC(=C(C=C1OC(=O)C)C(C)C)OCCN(C)C.Cl

IUPAC Name

[4-[2-(dimethylamino)ethoxy]-2-methyl-5-propan-2-ylphenyl] acetate;hydrochloride

InChIKey

IPWGSXZCDPTDEH-UHFFFAOYSA-N

INCHI

1S/C16H25NO3.ClH/c1-11(2)14-10-15(20-13(4)18)12(3)9-16(14)19-8-7-17(5)6;/h9-11H,7-8H2,1-6H3;1H

Isomere SMILES

CC1=CC(=C(C=C1OC(=O)C)C(C)C)OCCN(C)C.Cl

Molekulargewicht

315.84

Reaxy-Rn

3750837

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3750837&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Klasse Prenol lipids
      • Subclass Monoterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Klasse: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Aromatic monoterpenoids
• Alternative Parents: Monocyclic monoterpenoids Phenol esters Cumenes Phenylpropanes Phenoxy compounds Phenol ethers Toluenes Alkyl aryl ethers Trialkylamines Carboxylic acid esters Amino acids and derivatives Monocarboxylic acids and derivatives Organopnictogen compounds Organic oxides Organic chloride salts Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic monoterpenoid - P-cymene - Aromatic monoterpenoid - Phenol ester - Cumene - Phenylpropane - Phenoxy compound - Phenol ether - Alkyl aryl ether - Toluene - Monocyclic benzene moiety - Benzenoid - Amino acid or derivatives - Carboxylic acid ester - Tertiary amine - Tertiary aliphatic amine - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Ether - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic salt - Organic chloride salt - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring.
• 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.

DOI: 10.1186/s13321-016-0174-y

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GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

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SMN1 Tchem Survival motor neuron protein (34246 Activities)

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BLM Tchem Bloom syndrome protein (4248 Activities)

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GMNN Tbio Geminin (128009 Activities)

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Plasmodium falciparum (966862 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Molekulargewicht: 315.830 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 7
• Exact Mass: 315.16 Da
• Monoisotopic Mass: 315.16 Da
• Topological Polar Surface Area: 38.800 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 304.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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

XLogP3