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51-34-3 分子结构
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9-methyl-3-oxa-9-azatricyclo[3.3.1.0^{2,4}]nonan-7-yl 3-hydroxy-2-phenylpropanoate

ChemBase编号:627
分子式:C17H21NO4
平均质量:303.35294
单一同位素质量:303.14705816
SMILES和InChIs

SMILES:
O1C2C1C1N(C2CC(OC(=O)C(CO)c2ccccc2)C1)C
Canonical SMILES:
OCC(c1ccccc1)C(=O)OC1CC2N(C(C1)C1C2O1)C
InChI:
InChI=1S/C17H21NO4/c1-18-13-7-11(8-14(18)16-15(13)22-16)21-17(20)12(9-19)10-5-3-2-4-6-10/h2-6,11-16,19H,7-9H2,1H3
InChIKey:
STECJAGHUSJQJN-UHFFFAOYSA-N

引用这个纪录

CBID:627 http://www.chembase.cn/molecule-627.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
9-methyl-3-oxa-9-azatricyclo[3.3.1.0^{2,4}]nonan-7-yl 3-hydroxy-2-phenylpropanoate
IUPAC传统名
scopolamine
商标名
Atrochin
Atroquin
Atroscine Hydrobromide
Beldavrin
Buscopan
Epoxytropine Tropate
Euscopol
Hydroscine Hydrobromide
Hyocine F Hydrobromide
Hyosceine
Hyoscine
Hyoscine Bromide
Hyoscine Hydrobromide
Hyoscyine Hydrobromide
Hyosol
Hysco
Isopto Hyoscine
Isoscopil
Kwells
L-Hyoscine Hydrobromide
L-Scopolamine
Methscopolamine Bromide
Oscine
SEE
Scop
Scopamin
Scopine Tropate
Scopoderm-Tts
Scopolamine Bromide
Scopolamine Hydrobromide
Scopolamine Hydrobromide Trihydrate
Scopolamine Hyoscine
Scopolaminhydrobromid
Scopolaminium Bromide
Scopolammonium Bromide
Scopos
Sereen
Skopolamin
Tranaxine
Transcop
Transderm-Scop
Transderm-V
Triptone
Tropic Acid, Ester with Scopine
别名
Scopolamine
CAS号
51-34-3
PubChem SID
160964090
PubChem CID
5184

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
DrugBank DB00747 external link
PubChem 5184 external link
数据来源 数据ID 价格

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 15.14574  质子受体
质子供体 LogD (pH = 5.5) -0.56972116 
LogD (pH = 7.4) 0.7621961  Log P 0.8949523 
摩尔折射率 79.7213 cm3 极化性 32.014694 Å3
极化表面积 62.3 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P 1.4  LOG S -1.66 
溶解度 6.61e+00 g/l 

分子性质

分子性质

理化性质 生物活性(PubChem)
疏水性(logP)
0.8 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB00747 external link
Item Information
Drug Groups approved
Description An alkaloid from Solanaceae, especially Datura metel L. and Scopola carniolica. Scopolamine and its quaternary derivatives act as antimuscarinics like atropine, but may have more central nervous system effects. Among the many uses are as an anesthetic premedication, in urinary incontinence, in motion sickness, as an antispasmodic, and as a mydriatic and cycloplegic. [PubChem]
Indication For the treatment of excessive salivation, colicky abdominal pain, bradycardia, sialorrhoea, diverticulitis, irritable bowel syndrome and motion sickness.
Pharmacology Scopolamine is a muscarinic antagonist structurally similar to the neurotransmitter acetylcholine and acts by blocking the muscarinic acetylcholine receptors and is thus classified as an anticholinergic. Scopolamine has many uses including the prevention of motion sickness. It is not clear how Scopolamine prevents nausea and vomiting due to motion sickness. The vestibular part of the ear is very important for balance. When a person becomes disoriented due to motion, the vestibule sends a signal through nerves to the vomiting center in the brain, and vomiting occurs. Acetylcholine is a chemical that nerves use to transmit messages to each other. It is believe that Scopolamine prevents communication between the nerves of the vestibule and the vomiting center in the brain by blocking the action of acetylcholine. Scopolamine also may work directly on the vomiting center. Scopolamine must be taken before the onset of motion sickness to be effective.
Affected Organisms
Humans and other mammals
Absorption Bioavailability is 10 - 50%
Half Life 4.5 hours
Elimination Less than 10% of the total dose is excreted in the urine as parent and metabolites over 108 hours.
References
Putcha L, Cintron NM, Tsui J, Vanderploeg JM, Kramer WG: Pharmacokinetics and oral bioavailability of scopolamine in normal subjects. Pharm Res. 1989 Jun;6(6):481-5. [Pubmed]
External Links
Wikipedia
Drugs.com

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Putcha L, Cintron NM, Tsui J, Vanderploeg JM, Kramer WG: Pharmacokinetics and oral bioavailability of scopolamine in normal subjects. Pharm Res. 1989 Jun;6(6):481-5. Pubmed
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专利

专利

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