基本情報
- 標準SMILES
CCN(CC)CCOCCOC(=O)C1(c2ccccc2)CCCC1- InChIKey
CFJMRBQWBDQYMK-UHFFFAOYSA-N- 分子式
- C20H31NO3
- 平均分子量
- 333.5 g/mol
- 単同位体質量
- 333.23039385
概要
1-phenyl-1-cyclopentanecarboxylic acid 2-[2-(diethylamino)ethoxy]ethyl ester is a member of benzenes.
名称と識別子
- 優先名称
- Carbetapentane
- IUPAC
- 2-[2-(diethylamino)ethoxy]ethyl 1-phenylcyclopentane-1-carboxylate
- 現地名
- ペントキシベリン
- 英語名
- Pentoxyverine
- 分子式
- C20H31NO3
- 分子量
- 333.46
名称と別名
名称をさらに表示
データベース識別子
- CAS
77-23-6- PubChem CID
- 2562
- DTXSID
DTXSID9022734- ChEMBL
CHEMBL73234- ChEBI
CHEBI:94484- UNII
- 32C726X12W
- EC Number
- 201-014-1
- Nikkaji
- J4.198J
物性
構造計算による物性
- XLogP
- 3.8
- 極性表面積
- 38.8 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 4
- 回転可能結合数
- 11
- 重原子数
- 24
- 形式電荷
- 0
- 複雑度
- 356
実験および物理化学的性質
Drugs
Pharmaceuticals
Pharmaceuticals -> Listed in ZINC15
物理化学的性質
- 沸点
- 165 · 165-170 °C (1.33Pa)
- 比重(密度)
- 1.048 · 1.048±0.06 g/cm3(Predicted)
- 屈折率
- 1.499 · 1.4990-1.5010
- 貯蔵温度
- Refrigerator
- 溶解性
- ジクロロメタン(微量)、メタノール(微量)
- 酸解離定数(Pka)
- 9.69 · 9.69±0.25(Predicted)
- 外見
- 油
- 色
- クリアベリーダークレッドからブラウン
- CAS データベース
- 77 · 77-23-6(CAS DataBase Reference)
- NISTの化学物質情報
- 1 · 1-Cyclopentanecarboxylate, 2-(diethylaminoethoxy)ethyl-1-phenyl-(77-23-6)
安全と法規制
危険有害性情報
毒性情報
安全データ
- 毒性
- LD50 oral in rat: 150mg/kg
- 有毒物質データの
- 77-23-6(Hazardous Substances Data)
化学と産業
薬理情報
ATC Code
R - Respiratory system
QR - Respiratory system
Pharmacodynamics
Pentoxyverine induces an antitussive action. In animal studies, intraperitoneal administration of pentoxyverine inhibited citric-acid-induced cough in guinea-pigs _in vivo_. Some mice and rat studies suggest that pentoxyverine may also exert anticonvulsant activities without inducing a protective effect from NMDA-induced lethality. Protective effects against maximal electroshock-induced seizures in a dose-related fashion was also observed following either intraperitoneal or oral administration. In hERG-transfected cells, pentoxyverine inhibited the outward current of the hERG ion channel with half-maximal inhibition concentrations (IC50) of 3.0 µM. In rats receiving intrathecal administration, pentoxyverine exhibited dose-dependent spinal blockade with a more sensory-selective action over motor blockade. It induced a spinal blockade with a more sensory/nociceptive-selective action over motor blockade compared to lidocaine.
Mechanism of Action
While the mechanism of antitussive action of pentoxyverine is not fully understood, it is thought to be mediated via sigma-1 receptors expressed in the central nervous system. Pentoxyverine acts as an agonist at sigma receptors with the Ki of 75±28 nM, as demonstrated in a competitive binding assay. The function of sigma receptors on cough suppressant activities is unclear, however these receptors are highly expressed in the nucleus tractus solitarius (NTS) of the brainstem where the afferent fibres first synapse. NTS is located very close to the cough centre in the brainstem thus may function as a ‘gate' for the cough reflex and allow sigma-1 receptor agonists to modulate afferent activity prior to reaching the cough center. It is suggested that highly lipophilic sigma-1 agonists may penetrate the CNS following systemic administration. When administered as aerosols, sigma-1 receptor agonists may temporarily act in the periphery to modulate cough by acting activate sigma receptors expressed in the lungs. However there is limited evidence of peripheral localization of the sigma agonists following aerosol administration and the ruling out of systemic exposure. The local anesthesia action of pentoxyverine may occur through inhibition of voltage-gated Na(+) currents.
NUMBER OF DRUGS ARE KNOWN TO REDUCE COUGH AS RESULT OF THEIR CENTRAL ACTIONS, ALTHOUGH EXACT MECHANISMS ARE STILL NOT ENTIRELY CLEAR. /NONOPIOID ANTITUSSIVES/
Absorption, Distribution and Excretion
In humans, maximum plasma concentrations are achieved 1.2 hours after oral dosing.
No pharmacokinetic data available.
No pharmacokinetic data available.
No pharmacokinetic data available.
用途と製造
Uses
MEDICATION
Use (kg; approx.) in Germany (2009): >1000
応用分野
使用Carbetapentane is an antitussive anticonvulsant sigma site agonist.
上流・下流製品情報
上流原料
サプライヤー50 社
関連反応
現在のフィルター条件では反応記録がありません。
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