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71963-77-4 分子结构
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10-methoxy-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.0^{4,13}.0^{8,13}]hexadecane

ChemBase编号:4435
分子式:C16H26O5
平均质量:298.37464
单一同位素质量:298.17802393
SMILES和InChIs

SMILES:
CC1CCC2C(C)C(OC)OC3C42C1CCC(OO4)(O3)C
Canonical SMILES:
COC1OC2OC3(C)CCC4C2(C(C1C)CCC4C)OO3
InChI:
InChI=1S/C16H26O5/c1-9-5-6-12-10(2)13(17-4)18-14-16(12)11(9)7-8-15(3,19-14)20-21-16/h9-14H,5-8H2,1-4H3
InChIKey:
SXYIRMFQILZOAM-UHFFFAOYSA-N

引用这个纪录

CBID:4435 http://www.chembase.cn/molecule-4435.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
10-methoxy-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.0^{4,13}.0^{8,13}]hexadecane
IUPAC传统名
artemisinine,methyl ether (α)
商标名
Coartem
别名
Dihydroartemisinin methyl ether
Artemether
CAS号
71963-77-4
PubChem SID
160967867
PubChem CID
500199

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 DB06697 external link
PubChem 500199 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
质子受体 质子供体
LogD (pH = 5.5) 3.481392  LogD (pH = 7.4) 3.481392 
Log P 3.481392  摩尔折射率 74.6605 cm3
极化性 30.79904 Å3 极化表面积 46.15 Å2
可自由旋转的化学键 里宾斯基五规则 true 
Log P 3.02  LOG S -2.81 
溶解度 4.57e-01 g/l 

分子性质

分子性质

生物活性(PubChem)

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB06697 external link
Item Information
Drug Groups approved
Description Artemether is an antimalarial agent used to treat acute uncomplicated malaria. It is administered in combination with lumefantrine for improved efficacy. This combination therapy exerts its effects against the erythrocytic stages of Plasmodium spp. and may be used to treat infections caused by P. falciparum and unidentified Plasmodium species, including infections acquired in chloroquine-resistant areas.
Indication Artemether and lumefantrine combination therapy is indicated for the treatment of acute uncomplicated malaria caused by Plasmodium falciparum, including malaria acquired in chloroquine-resistant areas. May also be used to treat uncomplicated malaria when the Plasmodium species has not been identified. Indicated for use in adults and children greater than 5 kg.
Pharmacology In the body, artemether is metabolized into the active metabolite metabolite dihydroartemisinin. The drug works against the erythrocytic stages of P. falciparum by inhibiting nucleic acid and protein synthesis. Artemether is administered in combination with lumefantrine for improved efficacy. Artemether has a rapid onset of action and is rapidly cleared from the body. It is thought that artemether provides rapid symptomatic relief by reducing the number of malarial parasites. Lumefantrine has a much longer half life and is believed to clear residual parasites.
Toxicity Common side effects of combination artemether/lumefantrine therapy in adults include headache, anorexia, dizziness, and asthenia. Common side effects in children include pyrexia, cough, vomiting, anorexia, and headache. Possible serious adverse effects include QT prolongation, bullous eruption, urticaria, splenomegaly (9%), hepatomegaly (adults, 9%; children, 6%), hypersensitivty reaction, and angioedema.
Affected Organisms
Plasmodium
Biotransformation Rapidly metablized to its active metabolite, dihydroartemisinin.
Absorption Food increases absorption.
Half Life Artemether, 1.6 +/- 0.7 and 2.2 +/- 1.9 hr; Dihydroartemisinin, 1.6 +/- 0.6 and 2.2 +/- 1.5 hr
Protein Binding Artemether, 95.4%; Dihydroartemisinin, 47-76%
References
Artemether and Lumefantrine (2010). AHFS Drug Information [Electronic versionb]. Retrieved October 24, 2010.
Artemether/Lumefantrine (2010). DrugPoints? System [Electronic version]. Retrieved October 24, 2010.
Novartis. Coartem (artemether/lumefantrine) tablets prescribing information. East Hanover, NJ; 2010 Feb.
External Links
Wikipedia
RxList
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
  • Novartis. Coartem (artemether/lumefantrine) tablets prescribing information. East Hanover, NJ; 2010 Feb.
  • Artemether and Lumefantrine (2010). AHFS Drug Information [Electronic versionb]. Retrieved October 24, 2010.
  • Artemether/Lumefantrine (2010). DrugPoints? System [Electronic version]. Retrieved October 24, 2010.
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专利

专利

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