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Mechitazin

Mequitazine

HCID 4066
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TeilstruktursucheÄhnliche Strukturen suchen

Grundinformationen

CAS
29216-28-2
Standard-SMILES
c1ccc2c(c1)Sc1ccccc1N2CC1CN2CCC1CC2
InChIKey
HOKDBMAJZXIPGC-UHFFFAOYSA-N
Summenformel
C20H22N2S
Durchschnittliche Molmasse
322,5 g/mol
Monoisotopische Masse
322,15036988

Überblick

Mequitazine is a member of phenothiazines.

Namen und Bezeichner

Bevorzugter Name
Mequitazine
IUPAC
10-(1-azabicyclo[2.2.2]octan-3-ylmethyl)phenothiazine
Lokaler Name
Mechitazin
Englischer Name
MEQUITAZINE
Summenformel
C20H22N2S
Molmasse
322.47

Namen und Synonyme

mequitazine29216-28-2KitazeminMequitazinaMequitazinumQuitadrill10-(3-Quinuclidinylmethyl)phenothiazine3-Methylquinuclidinyl-10-phenothiazineDTXSID8023262NSC-303612Y463242LY210-(1-azabicyclo(2.2.2)oct-8-ylmethyl)phenothiazine
Weitere Namen anzeigen
ButixLM 209MircolMQ-A-88VigiganZesulanInstotalPrimalanNipolazin
DTXCID30326210-(1-azabicyclo(2.2.2)octan-3-ylmethyl)-10H-phenothiazine10-((3RS)-1-Azabicyclo(2.2.2)oct-3-ylmethyl)-10H-phenothiazine10-{1-azabicyclo[2.2.2]octan-3-ylmethyl}-10H-phenothiazineRefChem:811005R06AD07249-521-7Virginan

Datenbank-Bezeichner

CAS
29216-28-2
PubChem CID
4066
DTXSID
DTXSID8023262
ChEMBL
CHEMBL73451
ChEBI
CHEBI:31821
UNII
Y463242LY2
EC Number
249-521-7
Nikkaji
J342.305K

Eigenschaften

Berechnete Struktureigenschaften

XLogP
4,6
Polarare Oberfläche (TPSA)
31,8 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
3
Frei drehbare Bindungen
2
Schwere Atome
23
Formalladung
0
Komplexität
398

Experimentelle und physikochemische Eigenschaften

LogP4.7
Solubility · 2 Einträge

4.01e-03 g/L

>48.4 [ug/mL] (The mean of the results at pH 7.4)

Melting Point130.5 °C
Physical DescriptionSolid

Physikochemische Eigenschaften

Schmelzpunkt
143 · 143-145°C
Siedepunkt
469.4 · 469.4±24.0 °C(Predicted)
Dichte
1.133 · 1.1330 (rough estimate)
Brechungsindex
1.58 · 1.5800 (estimate)
storage temp.
Refrigerator
Löslichkeit
16 mg/mL · DMSO : 16 mg/mL (49.62 mM)
Wasserlöslichkeit
Insoluble in water
Aggregatzustand
powder to crystal
pka
10.43 · 10.43±0.33(Predicted)
Farbe
White to Almost white
Merck
14 · 14,5864
InChI
1S/C20H22N2S/c1-3-7-19-17(5-1)22(18-6-2-4-8-20(18)23-19)14-16-13-21-11-9-15(16)10-12-21/h1-8,15-16H,9-14H2
InChIKey
HOKDBMAJZXIPGC-UHFFFAOYSA-N
SMILES
S1c2c(cccc2)N(c5c1cccc5)CC3C4CCN(C3)CC4
CAS Datenbank
29216 · 29216-28-2(CAS DataBase Reference)
NIST chemische Informationen
Mequitazine(29216-28-2)

Sicherheit und Regulatorisches

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

GHS-Klassifizierung

GHS Classification · 4 Einträge

Danger

H301 (66.7%): Toxic if swallowed [Danger Acute toxicity, oral]

P261, P264, P264+P265, P270, P271, P272, P273, P280, P301+P316, P301+P317, P302+P352, P304+P340, P305+P354+P338, P317, P321, P330, P332+P317, P333+P317, P362+P364, P391, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 6 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Gefahrenhinweise

Hazard Classes and CategoriesAcute Tox. 3 (66.7%)

Toxikologische Informationen

Drug Induced Liver Injury · 4 Einträge

Drug-Induced Liver Injury Severity and Toxicity (DILIst)

Mequitazine

DILI Positive

DOI:10.1016/j.drudis.2019.09.022

Sicherheitsdaten

wgk
WGK 3
ridadr
UN 2811 6.1/PG III
hs_code
29349990
RTECS-Nr.
SP5080000
hazard_class
6.1
packing_group
III
Speicherklasse
6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
Hazard Classifications
Acute Tox. 3 Oral

Chemie und Industrie

Pharmakologische Informationen

ATC Code · 2 Einträge

R - Respiratory system

QR - Respiratory system

Pharmacodynamics · 1 Eintrag

In allergic reactions an allergen interacts with and cross-links surface IgE antibodies on mast cells and basophils. Once the mast cell-antibody-antigen complex is formed, a complex series of events occurs that eventually leads to cell-degranulation and the release of histamine (and other chemical mediators) from the mast cell or basophil. Once released, histamine can react with local or widespread tissues through histamine receptors. Histamine, acting on H<sub>1</sub>-receptors, produces pruritis, vasodilatation, hypotension, flushing, headache, tachycardia, and bronchoconstriction. Histamine also increases vascular permeability and potentiates pain. Mequitazine is a histamine H1 antagonist. It competes with histamine for the normal H<sub>1</sub>-receptor sites on effector cells of the gastrointestinal tract, blood vessels and respiratory tract. It provides effective, temporary relief of sneezing, watery and itchy eyes, and runny nose due to hay fever and other upper respiratory allergies.

Mechanism of Action · 1 Eintrag

Mequitazine binds to the histamine H1 receptor sites on effector cells in the gastrointestinal tract, blood vessels, and respiratory tract. This blocks the action of endogenous histamine, which subsequently leads to temporary relief of the negative symptoms brought on by histamine.

MeSH Pharmacological Classification · 1 Eintrag

Drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine. Included here are the classical antihistaminics that antagonize or prevent the action of histamine mainly in immediate hypersensitivity. They act in the bronchi, capillaries, and some other smooth muscles, and are used to prevent or allay motion sickness, seasonal rhinitis, and allergic dermatitis and to induce somnolence. The effects of blocking central nervous system H1 receptors are not as well understood.

Cellular LocationsMembrane
Metabolite PathwaysMequitazine H1-Antihistamine Action

Anwendungen

VerwendenIt is an antihistamine

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

Phenothiazin

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