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147127-20-6 分子结构
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({[(2R)-1-(6-amino-9H-purin-9-yl)propan-2-yl]oxy}methyl)phosphonic acid

ChemBase编号:185
分子式:C9H14N5O4P
平均质量:287.212321
单一同位素质量:287.07834058
SMILES和InChIs

SMILES:
P(=O)(O)(O)CO[C@@H](Cn1c2ncnc(N)c2nc1)C
Canonical SMILES:
C[C@H](Cn1cnc2c1ncnc2N)OCP(=O)(O)O
InChI:
InChI=1S/C9H14N5O4P/c1-6(18-5-19(15,16)17)2-14-4-13-7-8(10)11-3-12-9(7)14/h3-4,6H,2,5H2,1H3,(H2,10,11,12)(H2,15,16,17)/t6-/m1/s1
InChIKey:
SGOIRFVFHAKUTI-ZCFIWIBFSA-N

引用这个纪录

CBID:185 http://www.chembase.cn/molecule-185.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
({[(2R)-1-(6-amino-9H-purin-9-yl)propan-2-yl]oxy}methyl)phosphonic acid
IUPAC传统名
({[(2R)-1-(6-amino-9H-purin-9-yl)propan-2-yl]oxy}methyl)phosphonic acid
tenofovir
商标名
Apropovir
Viread
别名
泰诺福韦
(R)-9-(2-Phosphonomethoxypropyl)adenine
Apropovir
9-[2-(Phosphonomethoxy)propyl]adenine
Tenofovir
Tenofovir disoproxil
Tenofovir disoproxil fumarate
D,L-Tenofovir
TDF
PMPA
Tenofovir
Viread
PMPA
[[(1R)-2(6-Amino-9H-purin-9-yl)-1-methylethoxy]methyl]phosphonic Acid
(R)-9-(2-Phosphonomethoxypropyl)adenine
(R)-PMPA
GS-1278
CAS号
147127-20-6
147127-20-6
MDL号
MFCD00943794
PubChem SID
160963648
46508131
PubChem CID
464205

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 1.3504745  质子受体
质子供体 LogD (pH = 5.5) -3.55535 
LogD (pH = 7.4) -3.5490735  Log P -4.1293006 
摩尔折射率 67.535 cm3 极化性 25.71448 Å3
极化表面积 136.38 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P -1.51  LOG S -2.19 
溶解度 1.87e+00 g/l 

分子性质

分子性质

理化性质 安全信息 药理学性质 产品相关信息 生物活性(PubChem)
溶解度
13.4 mg/mL in distilled water at 25oC (disoproxil fumarate salt) expand 查看数据来源
Warm DMSO expand 查看数据来源
Warm Water expand 查看数据来源
外观
White to Off-White Solid expand 查看数据来源
熔点
280-282°C expand 查看数据来源
疏水性(logP)
-1.6 expand 查看数据来源
保存条件
-20°C expand 查看数据来源
-20°C Freezer expand 查看数据来源
保存注意事项
IRRITANT expand 查看数据来源
MSDS下载
下载链接 expand 查看数据来源
下载链接 expand 查看数据来源
TSCA收录
false expand 查看数据来源
作用靶点
Reverse transcriptase expand 查看数据来源
生物活性机理
Reverse transcriptase inhibitor expand 查看数据来源
纯度
95+% expand 查看数据来源
成盐信息
Free Base expand 查看数据来源
质检报告
下载链接 expand 查看数据来源
应用领域
Anti-HIV agent expand 查看数据来源
Antiretroviral drugs expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank Selleck Chemicals Selleck Chemicals TRC TRC
DrugBank -  DB00300 external link
Item Information
Drug Groups approved; investigational
Description Tenofovir, marketed by Gilead Sciences under the trade name Viread®, belongs to a class of antiretroviral drugs known as nucleotide analogue reverse transcriptase inhibitors (nRTIs), which block reverse transcriptase, an enzyme crucial to viral production in HIV-infected people. [Wikipedia]
Indication For use, in combination with other antiretroviral agents, for the treatment of HIV-1 infection.
Pharmacology Tenofovir belongs to a class of antiretroviral drugs known as nucleotide analogue reverse transcriptase inhibitors (NtRTIs), which block reverse transcriptase, an enzyme crucial to viral production in HIV-infected people. Tenofovir is currently in late-stage clinical trials for the treatment of hepatitis B. Tenofovir disoproxil fumarate is an acyclic nucleoside phosphonate diester analog of adenosine monophosphate. Tenofovir requires initial diester hydrolysis for conversion to tenofovir and subsequent phosphorylations by cellular enzymes to form tenofovir diphosphate. Tenofovir diphosphate is a weak inhibitor of mammalian DNA polymerases α, β, and mitochondrial DNA polymerase γ.
Toxicity Limited clinical experience at doses higher than the therapeutic dose of tenofovir 300 mg is available. In Study 901 tenofovir disoproxil fumarate 600 mg was administered to 8 patients orally for 28 days. No severe adverse reactions were reported. The effects of higher doses are not known.
Affected Organisms
Human Immunodeficiency Virus
Biotransformation Neither tenofovir disoproxil nor tenofovir are substrates of CYP450 enzymes.
Absorption The oral bioavailability in fasted patients is approximately 25%. Administration of food (high fat meal containing 40 to 50% fat) increases the oral bioavailability, with an increase in the AUC of approximately 40%.
Half Life Approximately 17 hours.
Protein Binding Very low: < 0.7% to human plasma proteins and < 7.2% to serum proteins
Distribution * 1.3 ± 0.6 L/kg [tenofovir 1.0 mg/kg]
* 1.2 ± 0.4 L/kg [tenofovir 3.0 mg/kg]
External Links
Wikipedia
RxList
PDRhealth
Drugs.com
Selleck Chemicals -  S1401 external link
Research Area: Infection
Biological Activity:
Tenofovir (Viread) is a drug used to treat human immunodeficiency virus (HIV) infection. Tenofovir is an antiviral drug called a nucleotide reverse transcriptase inhibitor. Tenofovir may reduce the amount of HIV in the blood and increase the number of CD4 cells (T-cells) in the blood. Tenofovir is used in combination with other drugs to treat the HIV virus. Tenofovir will not cure or prevent HIV infection or AIDS. [1]
Toronto Research Chemicals -  T018500 external link
Acyclic phosphonate nucleotide analogue; reverse transcriptase inhibitor. Used as an anti-HIV agent. Antiviral.

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • http://www.rxlist.com/atripla-drug.htm
  • Shaw, J.-P., et al.: Pharm. Res., 14, 1824 (1997)
  • Wyles, D., et al.: Clin Infect. Dis., 40, 174 (1997)
  • Peng, J., et al.: J. Clin. Pharmacol., 46, 265 (1997)
  • Seminari, E., et al.: J. Antimicrob. Chemother., 60, 831 (1997)
  • Eur. Pat., 1986, Ceskoslovenska, 206 459; CA, 106, 214308n
  • van Rompay, K.K.A. et al., Antimicrob. Agents Chemother., 1996, 40, 2586-2591
  • Balzarini, J. et al., Biochem. Biophys. Res. Commun., 1996, 219, 337-341
  • Arimilli, M.N. et al., Antiviral Chem. Chemother., 1997, 8, 557-564
  • Mulato, A.S. et al., Antiviral Res., 1997, 36, 91-97
  • Robbins, B.L. et al., Antimicrob. Agents Chemother., 1998, 42, 612-617; 1484-1487
  • Naesens, L. et al., Antimicrob. Agents Chemother., 1998, 42, 1568-1573
  • Hatse, S. et al., Int. J. Cancer, 1998, 76, 595-600
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专利

专利

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