StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
Huagongshe Open Project:[email protected]KI-Anbindung: llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.7.8
  1. Startseite
  2. /Verbindung

Alprenolol

HCID 2119
NotizenReaktionen
GrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
TeilstruktursucheÄhnliche Strukturen suchen

Grundinformationen

CAS
13655-52-2
Standard-SMILES
C=CCc1ccccc1OCC(O)CNC(C)C
InChIKey
PAZJSJFMUHDSTF-UHFFFAOYSA-N
Summenformel
C15H23NO2
Durchschnittliche Molmasse
249,35 g/mol
Monoisotopische Masse
249,17287898

Überblick

Alprenolol is a secondary alcohol that is propan-2-ol substituted by a 2-allylphenoxy group at position 1 and an isopropylamino group at position 3. It is a beta-adrenergic antagonist used as a antihypertensive, anti-arrhythmia and a sympatholytic agent. It has a role as a beta-adrenergic antagonist, an antihypertensive agent, an anti-arrhythmia drug and a sympatholytic agent. It is a secondary alcohol and a secondary amino compound.

Namen und Bezeichner

Bevorzugter Name
Alprenolol
IUPAC
1-(propan-2-ylamino)-3-(2-prop-2-enylphenoxy)propan-2-ol
Lokaler Name
Alprenolol
Englischer Name
Alprenolol
Summenformel
C15H23NO2
Molmasse
249.35

Namen und Synonyme

alprenolol13655-52-2AlfeprolAlprenololum1-(o-Allylphenoxy)-3-(isopropylamino)-2-propanol1-(2-Allylphenoxy)-3-isopropylamino-2-propanol1-(propan-2-ylamino)-3-(2-prop-2-enylphenoxy)propan-2-olDTXSID00451272-Propanol, 1-[(1-methylethyl)amino]-3-[2-(2-propenyl)phenoxy]-877K5MQ27WNSC-759561DTXCID8025127
Weitere Namen anzeigen
1-Isopropylamino-3-(2-allyl)phenoxypropan-2-olAlpheprolALLPRENOLOLdl-Alprenolol(RS)-AlprenololAlprenolol USP/EP/BP(-)-Alprenolol hydrate D-tartrate3-(o-Allylphenoxy)-1-isopropylamino-2-propanol1-(2-Allylphenoxy)-3-(isopropylamino)-2-propanol
CHEBI:512112-Propanol, 1-((1-methylethyl)amino)-3-(2-(2-propenyl)phenoxy)-{2-hydroxy-3-[2-(prop-2-en-1-yl)phenoxy]propyl}(propan-2-yl)aminealprenololoAptinDurilesAptin DurilesAptin-Duriles(2-hydroxy-3-(2-(prop-2-en-1-yl)phenoxy)propyl)(propan-2-yl)amine

Eigenschaften

Berechnete Struktureigenschaften

XLogP
3,1
Polarare Oberfläche (TPSA)
41,5 Ų
H-Brücken-Donoren
2
H-Brücken-Akzeptoren
3
Frei drehbare Bindungen
8
Schwere Atome
18
Formalladung
0
Komplexität
231

Experimentelle und physikochemische Eigenschaften

Chemical ClassesOther Uses -> Pharmaceuticals
LogP2.8
Solubility1.88e-01 g/L
Human DrugsPharmaceuticals
Melting Point · 2 Einträge

107-109 °C

107 - 109 °C

Physical DescriptionSolid
Dissociation Constants · 2 Einträge

9.51

9.6

Collision Cross Section · 3 Einträge

159.5 Ų [M+H]+ [CCS Type: TW; Method: Major Mix IMS/Tof Calibration Kit (Waters)]

163.63 Ų [M+Na]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

158.6 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

Physikochemische Eigenschaften

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Gefahrenhinweise

Other Safety InformationIMAP assessments - 2-Propanol, 1-[(1-methylethyl)amino]-3-[2-(2-propen-1-yl)phenoxy]-: Environment tier I assessment
Hazards SummaryAllergic contact dermatitis reported in pharmaceutical workers; [Kanerva, p. 1181-2]

Toxikologische Informationen

Adverse EffectsSkin Sensitizer - An agent that can induce an allergic reaction in the skin.

Sicherheitsdaten

ridadr
3249
risk_code
23/24/25-43
Toxizität
mammal (species unspecified),LD50,intraperitoneal,102mg/kg (102mg/kg),Pharmaceutical Chemistry Journal Vol. 8, Pg. 137, 1974.
hazard_code
T
safety_code
36/37/39-45
hazard_class
6.1(b)
packing_group
III

Chemie und Industrie

Pharmakologische Informationen

ATC Code · 2 Einträge

C - Cardiovascular system

QC - Cardiovascular system

Protein Binding80-90%
Pharmacodynamics · 1 Eintrag

Alprenolol is a non-selective beta-blocker used in the treatment of hypertension, edema, ventricular tachycardias, and atrial fibrillation. Alprenolol impairs AV node conduction and decreases sinus rate and may also increase plasma triglycerides and decrease HDL-cholesterol levels. Alprenolol is nonpolar and hydrophobic, with low to moderate lipid solubility. Alprenolol has little to no intrinsic sympathomimetic activity and, unlike some other beta-adrenergic blocking agents, alprenolol has little direct myocardial depressant activity and does not have an anesthetic-like membrane-stabilizing action.

Mechanism of Action · 1 Eintrag

Alprenolol non-selectively blocks beta-1 adrenergic receptors mainly in the heart, inhibiting the effects of epinephrine and norepinephrine resulting in a decrease in heart rate and blood pressure. Also, with a more minor effect, by binding beta-2 receptors in the juxtaglomerular apparatus, alprenolol inhibits the production of renin, thereby inhibiting angiotensin II and aldosterone production and therefore inhibits the vasoconstriction and water retention due to angiotensin II and aldosterone, respectively.

Biological Half-Life2-3 hours
Metabolism/MetabolitesHepatic. One of the active metabolites, 4-OH-alprenolol, is an active beta-blocker.
MeSH Pharmacological Classification · 4 Einträge

Drugs that bind to but do not activate beta-adrenergic receptors thereby blocking the actions of beta-adrenergic agonists. Adrenergic beta-antagonists are used for treatment of hypertension, cardiac arrhythmias, angina pectoris, glaucoma, migraine headaches, and anxiety.

Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade.

Zugehörige Reaktionen

0
Reaktionsaufzeichnung erstellen

Keine Reaktionsaufzeichnungen unter den aktuellen Filterkriterien.

Notizen zur Verbindung

Wird geladen…

Auf dieser SeiteGrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung

Datenbank-Bezeichner

CAS
13655-52-2
PubChem CID
2119
DTXSID
DTXSID0045127
ChEMBL
CHEMBL266195
ChEBI
CHEBI:51211
UNII
877K5MQ27W
EC Number
237-140-9
Nikkaji
J8.133G
Schmelzpunkt
57.5 °C · 57.5°C
Siedepunkt
392.45 °C · 392.45°C (rough estimate)
Dichte
1.0065 · 1.0065 (rough estimate)
Brechungsindex
1.525 · 1.5250 (estimate)
storage temp.
-20 °C · Store at -20°C
Löslichkeit
20 mg/ml; · DMF: 20 mg/ml; DMSO: 15 mg/ml; Ethanol: 5 mg/ml; PBS (pH 7.2): 1 mg/ml
Aggregatzustand
A crystalline solid
pka
9.63 · pKa 9.63 (Uncertain)
Farbe
White to off-white
Wasserlöslichkeit
366.9 mg/L · 366.9mg/L(22.5 ºC)
NIST chemische Informationen
2 · 2-Propanol, 1-[(1-methylethyl)amino]-3-[2-(2-propenyl)phenoxy]-(13655-52-2)

Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS.

Drugs that inhibit the actions of the sympathetic nervous system by any mechanism. The most common of these are the ADRENERGIC ANTAGONISTS and drugs that deplete norepinephrine or reduce the release of transmitters from adrenergic postganglionic terminals (see ADRENERGIC AGENTS). Drugs that act in the central nervous system to reduce sympathetic activity (e.g., centrally acting alpha-2 adrenergic agonists, see ADRENERGIC ALPHA-AGONISTS) are included here.

Cellular LocationsMembrane
Metabolite PathwaysAlprenolol Action Pathway

Verwendung und Herstellung

UsesUsed as an antihypertensive drug;
Use ClassificationPharmaceuticals

Anwendungen

BeschreibungOccupational cases of contact dermatitis caused by exposure to alprenolol have been reported within the pharmaceutical industry.

VerwendenAntiadrenergic (β-receptor).

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

NatriumtetrahydroboratAcetonHydrogenchloridAmmoniak, wasserfrei

Anbieter28 Anbieter

北京华美互利生物化工010-56205725 · [email protected]
艾吉析科技(上海)有限公司17717235263 · [email protected]
杭州摩库生物医药科技有限公司+86-057181025280; +8617767106207 · [email protected]
InvivoChem中国13549236410 · [email protected]
MedChemexpress LLC021-58955995 · [email protected]
上海喀露蓝科技有限公司18149758185 18149758185 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
上海肯恩化学科技有限公司13120367189;18621755571 · [email protected]
青岛海智微元生物科技有限公司18317699790 18317699790 · [email protected]
Alfa Chemistry1-516-6625404 · [email protected]
成都卡麦尔医药科技有限公司028-67136579 15828051124 · [email protected]
南通全益生物科技有限公司0513-66337626 18051384581 · [email protected]
启源(广东)医药化工有限公司18026564465 · [email protected]
风咏生物(AbMole)021-10000000 13000000000 · [email protected]
上海珞珐生化科技有限公司021-51111890 15317326293 · [email protected]
上海一飞生物科技有限公司021-65675885 18964387627 · [email protected]
上海芮晖化工科技有限公司021-31433387 15618786686 · [email protected]
上海立崎生物医学研究中心18014399201 · [email protected]
Shanghai Acmec Biochemical Technology Co., Ltd.+86-18621343501 · [email protected]
Musechem+1-800-259-7612 · [email protected]
范德(北京)生物科技有限责任公司15911056312 · [email protected]
上海迈瑞尔生化科技有限公司18621169109 · [email protected]
SHANGHAI KEAN TECHNOLOGY CO., LTD.+8613817748580 · [email protected]
ChemeGen 中国18818260767 · [email protected]
HANGZHOU CLAP TECHNOLOGY CO.,LTD86-571-88216897,88216896 13588875226 · [email protected]
南京世洲生物科技有限公司025-85560043 15850508050 · [email protected]
上海阿摩尔生物科技有限公司13370042665 18916960931 · [email protected]
InvivoChem+1-708-310-1919 +1-13798911105 · [email protected]
Ergänzende Hinweise · 1 Eintrag

DefinitionChEBI: A secondary alcohol that is propan-2-ol substituted by a 2-allylphenoxy group at position 1 and an isopropylamino group at position 3. It is a beta-adrenergic antagonist used as a antihypertensive, anti-arrhythmia and a sympatholytic agent.