Bisoprolol (BioDeep_00000001910)
Secondary id: BioDeep_00000397909
human metabolite blood metabolite
代谢物信息卡片
化学式: C18H31NO4 (325.2253)
中文名称: 比索洛尔
谱图信息:
最多检出来源 Homo sapiens(blood) 10.19%
分子结构信息
SMILES: CC(C)NCC(COC1=CC=C(C=C1)COCCOC(C)C)O
InChI: InChI=1S/C18H31NO4/c1-14(2)19-11-17(20)13-23-18-7-5-16(6-8-18)12-21-9-10-22-15(3)4/h5-8,14-15,17,19-20H,9-13H2,1-4H3
描述信息
Bisoprolol is a cardioselective β1-adrenergic blocking agent used for secondary prevention of myocardial infarction (MI), heart failure, angina pectoris and mild to moderate hypertension. Bisoprolol is structurally similar to metoprolol, acebutolol and atenolol in that it has two substituents in the para position of the benzene ring. The β1-selectivity of these agents is thought to be due in part to the large substituents in the para position. At lower doses (less than 20 mg daily), bisoprolol selectively blocks cardiac β1-adrenergic receptors with little activity against β2-adrenergic receptors of the lungs and vascular smooth muscle. Receptor selectivity decreases with daily doses of 20 mg or greater. Unlike propranolol and pindolol, bisoprolol does not exhibit membrane-stabilizing or sympathomimetic activity. Bisoprolol possesses a single chiral centre and is administered as a racemic mixture. Only l-bisoprolol exhibits significant β-blocking activity.
C - Cardiovascular system > C07 - Beta blocking agents > C07A - Beta blocking agents > C07AB - Beta blocking agents, selective
C78272 - Agent Affecting Nervous System > C29747 - Adrenergic Agent > C72900 - Adrenergic Antagonist
D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents > D013565 - Sympatholytics
D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents > D018674 - Adrenergic Antagonists
D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents
CONFIDENCE standard compound; EAWAG_UCHEM_ID 3013
CONFIDENCE standard compound; INTERNAL_ID 8595
CONFIDENCE standard compound; INTERNAL_ID 2677
同义名列表
25 个代谢物同义名
1-[(propan-2-yl)amino]-3-(4-{[2-(propan-2-yloxy)ethoxy]methyl}phenoxy)propan-2-ol; (+-)-1-((alpha-(2-Isopropoxyethoxy)-p-tolyl)oxy)-3-(isopropylamino)-2-propanol; (RS)-1-(4-(2-Isopropoxyethoxymethyl)phenoxy)-3-(isopropylamino)-2-propanol; (+-)-1-((a-(2-Isopropoxyethoxy)-p-tolyl)oxy)-3-(isopropylamino)-2-propanol; (+-)-1-((Α-(2-isopropoxyethoxy)-p-tolyl)oxy)-3-(isopropylamino)-2-propanol; 1-{4-[(2-isopropoxyethoxy)methyl]phenoxy}-3-(isopropylamino)propan-2-ol; Bisoprolol fumarate (1:1) salt, (+-)-isomer; Bisoprolol fumarate (2:1) salt, (+-)-isomer; Merck brand OF bisoprolol fumarate; Bisoprolol methanesulfonate salt; Bisoprolol, fumarate (1:1) salt; Bisoprolol, fumarate (2:1) salt; Hydrochloride, bisoprolol; Bisoprolol hydrochloride; Bisoprolol hemifumarate; Bisoprolol, (+-)-isomer; Bisoprolol, (-)-isomer; Fumarate, bisoprolol; Bisoprolol Fumarate; Bisoprolol fumerate; Bisoprololum; BISOPROLOL; Concor; Bisoprolol; Bisoprolol
数据库引用编号
31 个数据库交叉引用编号
- ChEBI: CHEBI:3127
- KEGG: C06852
- KEGGdrug: D02342
- PubChem: 2405
- HMDB: HMDB0014750
- Metlin: METLIN1353
- DrugBank: DB00612
- ChEMBL: CHEMBL645
- Wikipedia: Bisoprolol
- MeSH: Bisoprolol
- chemspider: 2312
- CAS: 104344-23-2
- CAS: 66722-44-9
- MoNA: AU267702
- MoNA: AU267706
- MoNA: EQ301301
- MoNA: EQ301305
- MoNA: EQ301304
- MoNA: EQ301302
- MoNA: AU267703
- MoNA: EQ301306
- MoNA: AU267701
- MoNA: SM859501
- MoNA: AU267705
- MoNA: AU267704
- MoNA: EQ301303
- PMhub: MS000001429
- PubChem: 9070
- NIKKAJI: J32.485J
- RefMet: Bisoprolol
- KNApSAcK: 3127
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
1 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Kamal Sharma, Hardik Desai, Neha Sharm, Mukesh Laddha, Kalpesh Hansora, Prashant Vazirani. To Evaluate the 'Real World' Clinical Performance of Bisoprolol in Post-Myocardial Infarction with Left Ventricular Dysfunction: Tenacity Study.
The Journal of the Association of Physicians of India.
2022 Apr; 70(4):11-12. doi:
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- Joshua Wong, Sameer Sharma, Jessica V Yao, Anuradha Aggarwal, Leeanne Grigg. COVID-19 mRNA vaccine (Comirnaty)-induced myocarditis.
The Medical journal of Australia.
2022 02; 216(3):122-123. doi:
10.5694/mja2.51394
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Medicine.
2021 Dec; 100(51):e28322. doi:
10.1097/md.0000000000028322
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The Canadian journal of cardiology.
2021 10; 37(10):1665-1667. doi:
10.1016/j.cjca.2021.05.010
. [PMID: 34118375] - Yuji Takahashi, Tomohiro Sonoo, Hidehiko Nakano, Hiromu Naraba, Hideki Hashimoto, Kensuke Nakamura. The influence of edema on the bisoprolol blood concentration after bisoprolol dermal patch application: A case-control study.
Medicine.
2021 Sep; 100(38):e27354. doi:
10.1097/md.0000000000027354
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2021 06; 22(2):271-276. doi:
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CPT: pharmacometrics & systems pharmacology.
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2020 Apr; 35(2):228-237. doi:
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2019 Dec; 59(12):64-71. doi:
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Molecular pharmacology.
2019 11; 96(5):629-640. doi:
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Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
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Scientific reports.
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Journal of cardiovascular pharmacology and therapeutics.
2019 07; 24(4):387-396. doi:
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Current drug safety.
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Clinical drug investigation.
2018 Dec; 38(12):1145-1154. doi:
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2018 11; 289(?):146-157. doi:
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Journal of pharmaceutical and biomedical analysis.
2018 Sep; 159(?):272-281. doi:
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The lancet. Diabetes & endocrinology.
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European journal of heart failure.
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Trials.
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European journal of drug metabolism and pharmacokinetics.
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Brain, behavior, and immunity.
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Pharmacology.
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Journal of clinical pharmacology.
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Journal of the American College of Cardiology.
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Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
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The Journal of pharmacy and pharmacology.
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