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ベタヒスチン

Betahistine

HCID 2366
ノートを作成反応を作成見積依頼を出す
印刷プレビュー
基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
部分構造検索類似構造を探す

基本情報

CAS
5638-76-6
標準SMILES
CNCCc1ccccn1
InChIKey
UUQMNUMQCIQDMZ-UHFFFAOYSA-N
分子式
C8H12N2
平均分子量
136.19 g/mol
単同位体質量
136.10004839

概要

Betahistine is an aminoalkylpyridine that is pyridine substituted by a 2-(methylamino)ethyl group at position 2. It acts as a histamine agonist and a vasodilator, and is thought to improve the microcirculation of the labyrinth, resulting in reduced endolymphatic pressure. It is used (generally as the hydrochloride or mesylate salt) to reduce the symptoms of vertigo, tinnitus, and hearing loss associated with Mnire's disease. It has a role as a vasodilator agent and a H1-receptor agonist. It is an aminoalkylpyridine and a secondary amino compound.

名称と識別子

優先名称
Betahistine
IUPAC
N-methyl-2-pyridin-2-ylethanamine
現地名
ベタヒスチン
英語名
Betahistine
分子式
C8H12N2
分子量
136.19

名称と別名

betahistine5638-76-6N-Methyl-2-pyridineethanamineVasomotal2-Pyridineethanamine, N-methyl-Betahistina2-[2-(Methylamino)ethyl]pyridineN-methyl-2-pyridin-2-ylethanamineBetahistinummethyl[2-(pyridin-2-yl)ethyl]amineBetaistina2-(2-(Methylamino)ethyl)pyridine
名称をさらに表示
N-メチルピリジン-2-エタンアミンN-メチル-2-ピリジンエタンアミンN-メチル-2-(2-ピリジル)エチルアミンベータヒスチンβ-ヒスチンN-メチルピリジン-2-(エタンアミン)2-(2-メチルアミノエチル)ピリジン2-[2-(メチルアミノ)エチル]ピリジン2-(メチルアミノエチル)ピリジンベタヒスチンN-メチル-2-ピリジンエタン-1-アミンメチル[2-(ピリジン-2-イル)エチル]アミンn-methyl-2-(pyridin-2-yl)ethan-1-amineY-G 14-d3PT 9 baseSerc baseβ-HistineNSC 42617-d3AKOS BBS-00002883Sinmenier (free base)
Vestibo(2-(2-Pyridyl)ethyl)methylamine[2-(2-Pyridyl)ethyl]methylamine2-(beta-Methylaminoethyl)pyridineHISTALEANX32KK4201DN-Methyl-2-(2-pyridinyl)ethanamineNSC-42617

物性

構造計算による物性

XLogP
0.4
極性表面積
24.9 Ų
水素結合供与体数
1
水素結合受容体数
2
回転可能結合数
3
重原子数
10
形式電荷
0
複雑度
83.3

実験および物理化学的性質

Drugs · 3 件

Pharmaceuticals -> Listed in ZINC15

Pharmaceuticals

Pharmaceuticals -> Used in Switzerland

LogP0.68
Boiling Point210.9±15.0 °C
Melting Point150-144
Physical DescriptionSolid
Dissociation Constants3.5, 9.7
Collision Cross Section132.35 Ų [M+K]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

物理化学的性質

沸点
113 · 113-114 °C30 mm Hg(lit.)
比重(密度)
0.984 g/mL · 0.984 g/mL at 25 °C(lit.)
蒸気圧
17.7 Pa · 17.7Pa at 25℃
屈折率
20 · n20/D 1.518(lit.)
闪点
206 °F · 206 °F
貯蔵温度
Keep in dark place,Inert atmosphere,Room temperature

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 4 件

Warning

H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 47 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Regulatory InformationREACH registered substance: Betahistine (EC: 227-086-4)
Hazard Classes and CategoriesSkin Irrit. 2 (100%)

毒性情報

Drug Induced Liver Injury · 5 件

Drug-Induced Liver Injury Severity and Toxicity (DILIst)

betahistine

DILI Positive

Oral

DOI:10.1016/j.drudis.2019.09.022

安全データ

wgk
2
tsca
TSCA listed
rtecs
UT5552000
hs_code
2933399990
risk_code
36/37/38
hazard_code
Xi,C
hazard_note
Corrosive
safety_code
26-37/39
Hazard Classifications
Eye Irrit. 2Skin Irrit. 2STOT SE 3

化学と産業

薬理情報

ATC Code · 3 件

N07CA01

N - Nervous system

QN - Nervous system

Protein BindingThe plasma protein binding of betahistine is reported to be less than 5%.
PharmacodynamicsThrough its actions on the histamine receptors, betahistine provides relief from vertigo associated with Ménière's disease.
Mechanism of Action · 2 件

OBE101 is a H1 receptor agonist and partial H3 receptor antagonist. Because inhibition of H1 receptors increases feeding, agonism of H1 receptors by OBE101 should reduce feeding. By also partially antagonizing H3, OBE101 impedes a negative feedback loop that essentially prolongs stimulation of the H1 receptors.

Vertigo is a disturbing sensation of movement caused by dysfunction of the labyrinth (inner ear), vestibular nerve, cerebellum, brainstem, or Central Nervous System (CNS). Vestibular forms of vertigo are often accompanied by auditory dysfunctions such as hyperacusis, hearing loss, and tinnitus. In most cases, adaptive mechanisms of the CNS lead to functional recovery after episodes of vertigo, however, syndromes such as Ménière's disease tend to cause the recurrence of vertigo symptoms. This significantly impacts the quality of life and the ability to carry out daily activities. **H1-receptor activity** The mechanism of action of betahistine is multifactorial. Ménière's disease is thought to result from a disruption of endolymphatic fluid homeostasis in the ear. Betahistine mainly acts as a histamine H1-receptor agonist. The stimulation of H1-receptors in the inner ear causes a vasodilatory effect leading to increased permeability of blood vessels and a reduction in endolymphatic pressure; this action prevents the rupture of the labyrinth, which can contribute to the hearing loss associated with Ménière's disease. Betahistine is also purported to act by reducing the asymmetrical functioning of sensory vestibular organs and increasing vestibulocochlear blood flow, relieving symptoms of vertigo. **H3-receptor activity** In addition to the above mechanisms, betahistine also acts as a histamine H3-receptor antagonist, increasing the turnover of histamine from postsynaptic histaminergic nerve receptors, subsequently leading to an increase in H1-agonist activity. H3-receptor antagonism elevates levels of neurotransmitters including serotonin in the brainstem, inhibiting the activity of vestibular nuclei, thus restoring proper balance and decreasing vertigo symptoms.

関連反応

64 件
反応記録を作成
HRID 14638 の反応式
HRID 14638反応物としてuspto-grants-2010_06
HRID 14687 の反応式
HRID 14687反応物としてuspto-grants-2010_06
HRID 17829 の反応式
HRID 17829反応物としてuspto-grants-2010_06
HRID 17833 の反応式
HRID 17833反応物としてuspto-grants-2010_06
HRID 33721 の反応式
HRID 33721反応物としてuspto-grants-2008_09
HRID 154598 の反応式
HRID 154598反応物としてTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
HRID 187445 の反応式
HRID 187445反応物としてTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
HRID 211212 の反応式
HRID 211212反応物としてTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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化合物ノート

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このページの内容基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
その他の操作
ノートを作成反応を作成見積依頼を出す

データベース識別子

CAS
5638-76-6
PubChem CID
2366
DTXSID
DTXSID3022665
ChEMBL
CHEMBL24441
ChEBI
CHEBI:35677
UNII
X32KK4201D
EC Number
227-086-4
Nikkaji
J8.042J
溶解性
Chloroform (Slightly), DMSO (Sparingly), Ethyl Acetate (Slightly), Methanol (Slightly)
酸解離定数(Pka)
3.46 · pKa 3.46 (Uncertain)
外見
油
色
薄黄色~黄色
水溶解度
1000 g/L · 1000g/L at 25℃
Merck
13 · 13,1181
InChI
1S/C8H12N2/c1-9-7-5-8-4-2-3-6-10-8/h2-4,6,9H,5,7H2,1H3
InChIKey
UUQMNUMQCIQDMZ-UHFFFAOYSA-N
SMILES
CNCCc1ccccn1
LogP
0.68 · 0.68
CAS データベース
5638 · 5638-76-6(CAS DataBase Reference)
EPAの化学物質情報
2 · 2-Pyridineethanamine, N-methyl- (5638-76-6)
ストレージクラス
10 - Combustible liquids
Biological Half-LifeThe half-life of betahistine is 3-4 hours.
Metabolism/MetabolitesBetahistine is metabolized primarily into the inactive metabolite 2-pyridylacetic acid. There is both clinical and in vitro evidence that monoamine oxidase enzymes are responsible for the metabolism of betahistine.
MeSH Pharmacological Classification · 2 件

Drugs used to cause dilation of the blood vessels.

Drugs that bind to and activate histamine receptors. Although they have been suggested for a variety of clinical applications histamine agonists have so far been more widely used in research than therapeutically.

Absorption, Distribution and Excretion · 3 件

When given orally, betahistine is rapidly and almost completely absorbed from the gastrointestinal tract. In the fasted state, Cmax is achieved within 1 hour of administration; in the fed state, Cmax is delayed, but the total drug absorption is similar. Food, therefore, has little effect on the absorption of betahistine.[A220563,16388]

Betahistine is mainly excreted in the urine; with approximately 85-91% being detected in urine samples within 24 hours of administration.

In a pharmacokinetic study of rats, betahistine was found to be distributed throughout the body. Human data for betahistine's volume of distribution is not readily available.

Cellular LocationsMembrane
Metabolite PathwaysBetahistine H1-Antihistamine Action

用途と製造

UsesUse (kg; approx.) in Germany (2009): >1000
General Manufacturing Information2-Pyridineethanamine, N-methyl-: INACTIVE
応用分野 · 2 件

説明Betahistine is an analogue of histamine with weak agonist properties at histamine H1 receptors and more potent antagonistic effects at histamine H3 receptors.This drug is broadly used worldwide, except for the USA, since it has not been approved by the US Food and Drug Administration. Betahistine is a structural analog of histamine that acts as a weak partial postsynaptic histamine H1 receptor agonist and presynaptic H3 receptor antagonist, with no effect on postsynaptic H2 receptors (Gbahou et al, 2010). The mechanism of action of the drug appears to depend mainly on its action on H3 receptors mediated by two metabolites, aminoethylpyridine and hydroxyethylpyridine (Bertich et al, 2014).

使用Betahistine is a vasodilator, a mild H1 histamine agonist, and a potent H3 histamine antagonist. The mechanism of action in Meniere's disease is unknown, but theories include reducing the endolymphatic pressure through improved circulation in the stria vascularis or inhibiting activity in the vestibular nuclei. It has been found to be a safe drug with a very low side effect profile. Betahistine was FDA approved for Meniere's disease in the US market for a short period of time in the 1970s, but approval was then rescinded due to lack of evidence supporting its efficacy. However, based on clinical experience and several observational studies, it is still widely used elsewhere in the world.

上流・下流製品情報

上流原料

2-ピコリン2-ピリジンエタノール2-ビニルピリジンメチルアミン 塩酸塩塩酸酢酸

下流製品

N-Methyl-N,N-bis(2-pyridylethyl)amineベタヒスチン塩酸塩