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21256-18-8 分子结构
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3-(diphenyl-1,3-oxazol-2-yl)propanoic acid

ChemBase编号:865
分子式:C18H15NO3
平均质量:293.3166
单一同位素质量:293.10519335
SMILES和InChIs

SMILES:
o1c(c(nc1CCC(=O)O)c1ccccc1)c1ccccc1
Canonical SMILES:
OC(=O)CCc1nc(c(o1)c1ccccc1)c1ccccc1
InChI:
InChI=1S/C18H15NO3/c20-16(21)12-11-15-19-17(13-7-3-1-4-8-13)18(22-15)14-9-5-2-6-10-14/h1-10H,11-12H2,(H,20,21)
InChIKey:
OFPXSFXSNFPTHF-UHFFFAOYSA-N

引用这个纪录

CBID:865 http://www.chembase.cn/molecule-865.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
3-(diphenyl-1,3-oxazol-2-yl)propanoic acid
IUPAC传统名
oxaprozin
商标名
Alvo
Daypro
Daypro Alta
Deflam
Voir
别名
4,5-Diphenyl-2-oxazolepropionic Acid
3-(4,5-Diphenyloxazol-2-yl)propionic Acid
Actirin
Alvo
Durapro
Duraprost
NSC 310839
Oxapro
Wy 21743
β-(4,5-Diphenyloxazol-2-yl)propionic Acid
4,5-Diphenyl-2-oxazolepropanoic acid
Daypro
Oxaprozin
Oxaprozin
3-(4,5-Diphenyl-1,3-oxazol-2-yl)propanoic acid 97%
3-(4,5-diphenyl-1,3-oxazol-2-yl)propanoic acid
Oxaprozina [INN-Spanish]
Oxaprozine [INN-French]
Oxaprozinum [INN-Latin]
Oxaprozin
CAS号
21256-18-8
EC号
244-296-1
MDL号
MFCD00215977
PubChem SID
160964328
46506429
24278617
PubChem CID
4614

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 4.953937  质子受体
质子供体 LogD (pH = 5.5) 2.8090506 
LogD (pH = 7.4) 1.0501883  Log P 3.4633667 
摩尔折射率 81.8793 cm3 极化性 34.290295 Å3
极化表面积 63.33 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P 3.33  LOG S -3.96 
溶解度 3.25e-02 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
DMSO expand 查看数据来源
Insoluble expand 查看数据来源
Methanol expand 查看数据来源
外观
solid expand 查看数据来源
White Solid expand 查看数据来源
熔点
154-163°C expand 查看数据来源
161-163°C expand 查看数据来源
疏水性(logP)
2.948 expand 查看数据来源
3.7 expand 查看数据来源
保存条件
Refrigerator expand 查看数据来源
保存注意事项
Harmful expand 查看数据来源
RTECS编号
RP6990000 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
德国WGK号
3 expand 查看数据来源
个人保护装置
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand 查看数据来源
作用靶点
Others expand 查看数据来源
相关基因信息
human ... PTGIR(5739) expand 查看数据来源
纯度
95% expand 查看数据来源
97% 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
Empirical Formula (Hill Notation)
C18H15NO3 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank Sigma Aldrich Sigma Aldrich TRC TRC
DrugBank -  DB00991 external link
Item Information
Drug Groups approved
Description Oxaprozin is a non-narcotic, non-steroidal anti-inflammatory drug (NSAID), used to relieve the inflammation, swelling, stiffness, and joint pain associated with osteoarthritis and rheumatoid arthritis.
Indication Used to relieve the inflammation, swelling, stiffness, and joint pain associated with rheumatoid arthritis and osteoarthritis.
Pharmacology Oxaprozin is a nonsteroidal anti-inflammatory drug (NSAID) with analgesic and antipyretic properties. Oxaprozin is used to treat rheumatoid arthritis, osteoarthritis, dysmenorrhea, and to alleviate moderate pain.
Toxicity Oral, mouse: LD50 = 1210 mg/kg; Oral, rabbit: LD50 = 172 mg/kg; Oral, rat: LD50 = 4470 mg/kg
Affected Organisms
Humans and other mammals
Biotransformation Hepatic. Ester and ether glucuronide are the major conjugated metabolites of oxaprozin, and do not have significant pharmacologic activity.
Absorption Oxaprozin is 95% absorbed after oral administration. Food may reduce the rate of absorption of oxaprozin, but the extent of absorption is unchanged. Antacids do not significantly affect the extent and rate of oxaprozin absorption.
Half Life 54.9 hours
Protein Binding >99.5% bound to albumin
Elimination Oxaprozin is expected to be excreted in human milk based on its physical-chemical properties; however, the amount of oxaprozin excreted in breast milk has not been evaluated. Approximately 95% of oxaprozin is metabolized by the liver. Approximately 5% of the oxaprozin dose is excreted unchanged in the urine. Sixty-five percent (65%) of the dose is excreted in the urine and 35% in the feces as metabolite.
Biliary excretion of unchanged oxaprozin is a minor pathway. Several oxaprozin metabolites have been identified in human urine or feces.
Distribution * 11 to 17 L/70 kg
References
Heller B, Tarricone R: Oxaprozin versus diclofenac in NSAID-refractory periarthritis pain of the shoulder. Curr Med Res Opin. 2004 Aug;20(8):1279-90. [Pubmed]
Zhou XP, Zhang MX, Sun W, Yang XH, Wang GS, Sui DY, Yu XF, Qu SC: Design, synthesis, and in-vivo evaluation of 4,5-diaryloxazole as novel nonsteroidal anti-inflammatory drug. Biol Pharm Bull. 2009 Dec;32(12):1986-90. [Pubmed]
External Links
Wikipedia
RxList
Drugs.com
Sigma Aldrich -  O9637 external link
Application
Anti-inflammatory
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. O9637.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.
Toronto Research Chemicals -  O845400 external link
Oxaprozin is an anti-inflammatory drug. Oxaprozin was comparable to Aspirin (A687780).

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Heller B, Tarricone R: Oxaprozin versus diclofenac in NSAID-refractory periarthritis pain of the shoulder. Curr Med Res Opin. 2004 Aug;20(8):1279-90. PubmedZhou XP, Zhang MX, Sun W, Yang XH, Wang GS, Sui DY, Yu XF, Qu SC: Design, synthesis, and in-vivo evaluation of 4,5-diaryloxazole as novel nonsteroidal anti-inflammatory drug. Biol Pharm Bull. 2009 Dec;32(12):1986-90. Pubmed
  • Whitehouse, M.W., et al.: Biochem. Pharmacol., 20, 2309 (1971)
  • Janssen, F.W., et al.: Drug Metab. Dispos., 6, 465 (1971)
  • Shriver, D.A., et al.: Toxicol. Appl. Pharmacol., 42, 75 (1971)
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专利

专利

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