基本情報
- 標準SMILES
CC(C)(C)NC[C@H](O)COc1cccc2c1CCCC2=O.Cl- InChIKey
DNTDOBSIBZKFCP-YDALLXLXSA-N- 分子式
- C17H26ClNO3
- 平均分子量
- 327.8 g/mol
- 単同位体質量
- 327.16012137
概要
Levobunolol hydrochloride is a hydrochloride obtained by combining equimolar amounts of levobunolol and hydrochloric acid. A non-selective beta-adrenergic antagonist used for treatment of glaucoma. It has a role as a beta-adrenergic antagonist and an antiglaucoma drug. It contains a levobunolol(1+).
名称と識別子
- 優先名称
- Levobunolol Hydrochloride
- IUPAC
- 5-[(2S)-3-(tert-butylamino)-2-hydroxypropoxy]-3,4-dihydro-2H-naphthalen-1-one;hydrochloride
名称と別名
名称をさらに表示
データベース識別子
- CAS
27912-14-7- PubChem CID
- 5284409
- DTXSID
DTXSID6020777- ChEMBL
CHEMBL1201177- ChEBI
CHEBI:6439- UNII
- O90S49LDHH
- EC Number
- 248-725-3
物性
構造計算による物性
- 極性表面積
- 58.6 Ų
- 水素結合供与体数
- 3
- 水素結合受容体数
- 4
- 回転可能結合数
- 6
- 重原子数
- 22
- 形式電荷
- 0
- 複雑度
- 350
実験および物理化学的性質
Human Drugs
FDA approved drugs -> Active ingredient
FDA approved drugs -> Active ingredient
安全と法規制
GHS分類
GHS Classification
This chemical does not meet GHS hazard criteria for 2.1% (1 of 48) of reports.
Warning
H302 (97.9%): Harmful if swallowed [Warning Acute toxicity, oral]
P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 48 reports by companies from 3 notifications to the ECHA C&L Inventory.
危険有害性情報
化学と産業
薬理情報
FDA Pharmacological Classification
LEVOBUNOLOL HYDROCHLORIDE
beta-Adrenergic Blocker [EPC]; Adrenergic beta-Antagonists [MoA]
MeSH Pharmacological Classification
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.
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.
関連反応
関連ノート
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