etodolac (BioDeep_00000397851)

Main id: BioDeep_00000001784

 


代谢物信息卡片


etodolac

化学式: C17H21NO3 (287.1521)
中文名称: 依托度酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCC1=C2C(=CC=C1)C3=C(N2)C(OCC3)(CC)CC(=O)O
InChI: InChI=1S/C17H21NO3/c1-3-11-6-5-7-12-13-8-9-21-17(4-2,10-14(19)20)16(13)18-15(11)12/h5-7,18H,3-4,8-10H2,1-2H3,(H,19,20)

描述信息

M - Musculo-skeletal system > M01 - Antiinflammatory and antirheumatic products > M01A - Antiinflammatory and antirheumatic products, non-steroids > M01AB - Acetic acid derivatives and related substances
D018501 - Antirheumatic Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D016861 - Cyclooxygenase Inhibitors
D004791 - Enzyme Inhibitors > D016861 - Cyclooxygenase Inhibitors > D052246 - Cyclooxygenase 2 Inhibitors
C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic
D006133 - Growth Substances > D010937 - Plant Growth Regulators > D007210 - Indoleacetic Acids
D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents
D002491 - Central Nervous System Agents > D000700 - Analgesics
D000893 - Anti-Inflammatory Agents
CONFIDENCE standard compound; EAWAG_UCHEM_ID 3308

同义名列表

2 个代谢物同义名

etodolac; Etodolac



数据库引用编号

28 个数据库交叉引用编号

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)

0 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。

亚细胞结构定位 关联基因列表
Cytoplasm 14 ALB, ALOX5, BCL2, BIRC5, CASP3, CASP8, CASP9, CCND1, CDH1, CDKN1A, CTNNB1, PTGS1, PTGS2, RXRA
Peripheral membrane protein 3 ALOX5, PTGS1, PTGS2
Endoplasmic reticulum membrane 3 BCL2, PTGS1, PTGS2
Nucleus 12 ALB, BCL2, BIRC5, CASP3, CASP8, CASP9, CCND1, CDH1, CDKN1A, CTNNB1, PCNA, RXRA
cytosol 14 ALB, ALOX5, BCL2, BIRC5, CASP3, CASP8, CASP9, CCND1, CDH1, CDKN1A, CTNNB1, CTSH, GPT, RXRA
nuclear body 2 CDKN1A, PCNA
trans-Golgi network 1 CDH1
centrosome 4 ALB, CCND1, CTNNB1, PCNA
nucleoplasm 10 ALOX5, BIRC5, CASP3, CASP8, CCND1, CDH1, CDKN1A, CTNNB1, PCNA, RXRA
RNA polymerase II transcription regulator complex 1 RXRA
Cell membrane 4 CDH1, CTNNB1, TNF, TRPA1
lamellipodium 3 CASP8, CDH1, CTNNB1
Multi-pass membrane protein 1 TRPA1
Synapse 1 CTNNB1
cell cortex 1 CTNNB1
cell junction 2 CDH1, CTNNB1
cell surface 1 TNF
glutamatergic synapse 3 CASP3, CDH1, CTNNB1
Golgi apparatus 3 ALB, CDH1, PTGS1
neuronal cell body 2 CASP3, TNF
postsynapse 1 CDH1
presynaptic membrane 1 CTNNB1
Cytoplasm, cytosol 1 ALOX5
Lysosome 1 CTSH
endosome 1 CDH1
plasma membrane 4 CDH1, CTNNB1, TNF, TRPA1
Membrane 4 BCL2, CDH1, CTNNB1, TRPA1
basolateral plasma membrane 1 CTNNB1
caveola 1 PTGS2
extracellular exosome 7 ALB, CDH1, CTNNB1, CTSH, GPT, PCNA, PTGS1
endoplasmic reticulum 3 ALB, BCL2, PTGS2
extracellular space 5 ALB, ALOX5, CTSH, IL6, TNF
perinuclear region of cytoplasm 4 ALOX5, CDH1, CDKN1A, CTNNB1
Schaffer collateral - CA1 synapse 1 CTNNB1
adherens junction 2 CDH1, CTNNB1
apicolateral plasma membrane 1 CTNNB1
bicellular tight junction 2 CCND1, CTNNB1
mitochondrion 4 BCL2, CASP8, CASP9, RXRA
protein-containing complex 8 ALB, BCL2, BIRC5, CASP8, CASP9, CDKN1A, CTNNB1, PTGS2
intracellular membrane-bounded organelle 2 CTSH, PTGS1
Microsome membrane 2 PTGS1, PTGS2
postsynaptic density 1 CASP3
Single-pass type I membrane protein 1 CDH1
Secreted 2 ALB, IL6
extracellular region 6 ALB, ALOX5, CDH1, CTSH, IL6, TNF
cytoplasmic side of plasma membrane 1 CDH1
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 2 BCL2, CASP8
anchoring junction 1 ALB
transcription regulator complex 2 CTNNB1, RXRA
photoreceptor outer segment 1 PTGS1
Nucleus membrane 3 ALOX5, BCL2, CCND1
Bcl-2 family protein complex 1 BCL2
nuclear membrane 4 ALOX5, BCL2, CCND1, CDH1
external side of plasma membrane 1 TNF
actin cytoskeleton 1 CDH1
Z disc 1 CTNNB1
beta-catenin destruction complex 1 CTNNB1
microtubule cytoskeleton 1 BIRC5
nucleolus 1 CDKN1A
Wnt signalosome 1 CTNNB1
midbody 1 BIRC5
apical part of cell 1 CTNNB1
cell-cell junction 1 CTNNB1
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
postsynaptic membrane 1 CTNNB1
Cell projection, lamellipodium 1 CASP8
Cytoplasm, perinuclear region 1 ALOX5
Membrane raft 1 TNF
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 CTNNB1
Cytoplasm, cytoskeleton, spindle 1 BIRC5
focal adhesion 1 CTNNB1
microtubule 1 BIRC5
spindle 1 BIRC5
Cell junction, adherens junction 2 CDH1, CTNNB1
flotillin complex 2 CDH1, CTNNB1
collagen-containing extracellular matrix 1 CTSH
fascia adherens 1 CTNNB1
lateral plasma membrane 2 CDH1, CTNNB1
interphase microtubule organizing center 1 BIRC5
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
receptor complex 1 RXRA
neuron projection 2 PTGS1, PTGS2
ciliary basal body 1 ALB
chromatin 2 PCNA, RXRA
stereocilium bundle 1 TRPA1
phagocytic cup 1 TNF
cell periphery 1 CTNNB1
Chromosome 1 BIRC5
cytoskeleton 1 CASP8
Cytoplasm, cytoskeleton, cilium basal body 1 CTNNB1
centriole 2 ALB, BIRC5
cytoplasmic ribonucleoprotein granule 1 CTSH
Golgi apparatus, trans-Golgi network 1 CDH1
spindle pole 2 ALB, CTNNB1
nuclear replication fork 1 PCNA
chromosome, telomeric region 1 PCNA
nuclear chromosome 1 BIRC5
blood microparticle 1 ALB
postsynaptic density, intracellular component 1 CTNNB1
microvillus membrane 1 CTNNB1
nuclear envelope 1 ALOX5
Nucleus envelope 1 ALOX5
Endomembrane system 2 CTNNB1, PTGS1
Chromosome, centromere 1 BIRC5
Chromosome, centromere, kinetochore 1 BIRC5
euchromatin 1 CTNNB1
cell body 1 CASP8
replication fork 1 PCNA
myelin sheath 1 BCL2
ficolin-1-rich granule lumen 2 ALOX5, CTSH
secretory granule lumen 2 ALOX5, CTSH
endoplasmic reticulum lumen 3 ALB, IL6, PTGS2
nuclear matrix 1 ALOX5
transcription repressor complex 1 CCND1
male germ cell nucleus 1 PCNA
platelet alpha granule lumen 1 ALB
tertiary granule lumen 1 CTSH
kinetochore 1 BIRC5
beta-catenin-TCF complex 1 CTNNB1
anaphase-promoting complex 1 CDH1
Nucleus matrix 1 ALOX5
nuclear envelope lumen 1 ALOX5
apoptosome 1 CASP9
chromosome, centromeric region 1 BIRC5
presynaptic active zone cytoplasmic component 1 CTNNB1
nuclear lamina 1 PCNA
chromosome passenger complex 1 BIRC5
[Isoform 2]: Nucleus 1 CDH1
cytoplasmic microtubule 1 BIRC5
protein-DNA complex 1 CTNNB1
spindle microtubule 1 BIRC5
survivin complex 1 BIRC5
CD95 death-inducing signaling complex 1 CASP8
death-inducing signaling complex 2 CASP3, CASP8
ripoptosome 1 CASP8
apical junction complex 1 CDH1
Cell junction, desmosome 1 CDH1
desmosome 1 CDH1
catenin complex 2 CDH1, CTNNB1
cyclin-dependent protein kinase holoenzyme complex 3 CCND1, CDKN1A, PCNA
alveolar lamellar body 1 CTSH
multivesicular body lumen 1 CTSH
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
interleukin-6 receptor complex 1 IL6
Nucleus intermembrane space 1 ALOX5
BAD-BCL-2 complex 1 BCL2
cyclin D1-CDK4 complex 1 CCND1
PCNA complex 1 PCNA
PCNA-p21 complex 2 CDKN1A, PCNA
replisome 1 PCNA
beta-catenin-TCF7L2 complex 1 CTNNB1
cyclin D1-CDK6 complex 1 CCND1
beta-catenin-ICAT complex 1 CTNNB1
Scrib-APC-beta-catenin complex 1 CTNNB1
ciliary transition fiber 1 ALB
caspase complex 1 CASP9
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Poonam Patil, Atul Shirkhedkar. Nanostructured Etodolac Carriers in Transdermal Gel: Optimization and Characterization. Pharmaceutical nanotechnology. 2023 Jun; 11(3):276-293. doi: 10.2174/2211738511666230111110340. [PMID: 36635925]
  • Anna Czajkowska-Kośnik, Emilia Szymańska, Katarzyna Winnicka. Nanostructured Lipid Carriers (NLC)-Based Gel Formulations as Etodolac Delivery: From Gel Preparation to Permeation Study. Molecules (Basel, Switzerland). 2022 Dec; 28(1):. doi: 10.3390/molecules28010235. [PMID: 36615429]
  • Marwa Ibrahim Helmy, Samah Sabry Saad, Maha Abdelmonem Hegazy, Ahmed Salah Fayed. Sensitive and selective LC-MS/MS for the determination of tolperisone and etodolac in human plasma and application to a pharmacokinetic study. Journal of separation science. 2022 May; 45(10):1646-1655. doi: 10.1002/jssc.202100991. [PMID: 35233941]
  • Syed Nazrin Ruhina Rahman, Oly Katari, Datta Maroti Pawde, Gopi Sumanth Bhaskar Boddeda, Abhinab Goswami, Srinivasa Rao Mutheneni, Tamilvanan Shunmugaperumal. Application of Design of Experiments® Approach-Driven Artificial Intelligence and Machine Learning for Systematic Optimization of Reverse Phase High Performance Liquid Chromatography Method to Analyze Simultaneously Two Drugs (Cyclosporin A and Etodolac) in Solution, Human Plasma, Nanocapsules, and Emulsions. AAPS PharmSciTech. 2021 May; 22(4):155. doi: 10.1208/s12249-021-02026-6. [PMID: 33987739]
  • Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. Cell reports. 2021 04; 35(4):109040. doi: 10.1016/j.celrep.2021.109040. [PMID: 33910017]
  • Michael R Duff, Scott A Gabel, Lars C Pedersen, Eugene F DeRose, Juno M Krahn, Elizabeth E Howell, Robert E London. The Structural Basis for Nonsteroidal Anti-Inflammatory Drug Inhibition of Human Dihydrofolate Reductase. Journal of medicinal chemistry. 2020 08; 63(15):8314-8324. doi: 10.1021/acs.jmedchem.0c00546. [PMID: 32658475]
  • Sonia T Hassib, Ghaneya S Hassan, Asmaa A El-Zaher, Marwa A Fouad, Omnia A Abd El-Ghafar, Enas A Taha. Synthesis and biological evaluation of new prodrugs of etodolac and tolfenamic acid with reduced ulcerogenic potential. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences. 2019 Dec; 140(?):105101. doi: 10.1016/j.ejps.2019.105101. [PMID: 31639436]
  • Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular pharmacology. 2019 11; 96(5):629-640. doi: 10.1124/mol.119.115964. [PMID: 31515284]
  • Malek Hassan, Usama Alshana. Switchable-hydrophilicity solvent liquid-liquid microextraction of non-steroidal anti-inflammatory drugs from biological fluids prior to HPLC-DAD determination. Journal of pharmaceutical and biomedical analysis. 2019 Sep; 174(?):509-517. doi: 10.1016/j.jpba.2019.06.023. [PMID: 31238298]
  • In-Hwan Baek. Pharmacokinetic modeling and simulation of etodolac following single oral administration in dogs. Xenobiotica; the fate of foreign compounds in biological systems. 2019 Aug; 49(8):981-986. doi: 10.1080/00498254.2018.1524185. [PMID: 30216103]
  • Noha Khalifa Abo Aasy, Doaa Ragab, Marwa Ahmed Sallam, Doaa A Abdelmonsif, Rania G Aly, Kadria A Elkhodairy. A comparative study: the prospective influence of nanovectors in leveraging the chemopreventive potential of COX-2 inhibitors against skin cancer. International journal of nanomedicine. 2019; 14(?):7561-7581. doi: 10.2147/ijn.s218905. [PMID: 31571864]
  • Rita Haldar, Lee Shaashua, Hagar Lavon, Yasmin A Lyons, Oded Zmora, Eran Sharon, Yehudit Birnbaum, Tanir Allweis, Anil K Sood, Iris Barshack, Steve Cole, Shamgar Ben-Eliyahu. Perioperative inhibition of β-adrenergic and COX2 signaling in a clinical trial in breast cancer patients improves tumor Ki-67 expression, serum cytokine levels, and PBMCs transcriptome. Brain, behavior, and immunity. 2018 10; 73(?):294-309. doi: 10.1016/j.bbi.2018.05.014. [PMID: 29800703]
  • Akira Ooki, Asma Begum, Luigi Marchionni, Christopher J VandenBussche, Shifeng Mao, Max Kates, Mohammad Obaidul Hoque. Arsenic promotes the COX2/PGE2-SOX2 axis to increase the malignant stemness properties of urothelial cells. International journal of cancer. 2018 07; 143(1):113-126. doi: 10.1002/ijc.31290. [PMID: 29396848]
  • Yin Zhou, Paula Hertel, Jennifer Cu. Case 5: Large Amounts of Urine Bilirubin on Urine Dipstick in a 14-year-old Girl. Pediatrics in review. 2017 Sep; 38(9):440. doi: 10.1542/pir.2015-0068. [PMID: 28864738]
  • Il-Dong Song, Ju-Seop Kang, Hyun-Jin Kim, Se-Mi Kim, Dong-Xu Zhao, Shin-Hee Kim, Min-Young Chun, Kyu-Hyun Lee. Quantification of Etodolac in Human Plasma for Pharmacokinetics and Bioequivalence Studies in 27 Korean Subjects. Drug metabolism letters. 2017; 10(4):286-294. doi: 10.2174/1872312811666170116151004. [PMID: 28093968]
  • S Sarıözkan, G Türk, P Çıkla-Süzgün, M Güvenç, A Yüce, A H Yay, F Cantürk, Ş G Küçükgüzel. Effect of etodolac hydrazone, a new compound synthesised from etodolac, on spermatozoon quality, testicular lipid peroxidation, apoptosis and spermatozoon DNA integrity. Andrologia. 2016 Mar; 48(2):177-88. doi: 10.1111/and.12429. [PMID: 25929857]
  • Carolina de Miranda Silva, Adriana Rocha, Eduardo Tozatto, Lucienir Maria da Silva, Eduardo Antônio Donadi, Vera Lucia Lanchote. Enantioselective analysis of etodolac in human plasma by LC-MS/MS: Application to clinical pharmacokinetics. Journal of pharmaceutical and biomedical analysis. 2016 Feb; 120(?):120-6. doi: 10.1016/j.jpba.2015.12.009. [PMID: 26723001]
  • Ismail I Hewala, Marwa S Moneeb, Hatem A Elmongy, Abdel-Aziz M Wahbi. Enantioselective HPLC-DAD method for the determination of etodolac enantiomers in tablets, human plasma and application to comparative pharmacokinetic study of both enantiomers after a single oral dose to twelve healthy volunteers. Talanta. 2014 Dec; 130(?):506-17. doi: 10.1016/j.talanta.2014.07.011. [PMID: 25159440]
  • Askin Ender Topal, Hasan Akkoc, Ilker Kelle, Sedat Yilmaz, Derya Topal, Murat Akkus. Impact of N-acetylcysteine and etodolac treatment on systolic and diastolic function in a rat model of myocardial steatosis induced by high-fat-diet. Endocrine, metabolic & immune disorders drug targets. 2014; 14(4):313-9. doi: 10.2174/1871530314666141028144702. [PMID: 25348332]
  • Shenglan Wang, Yi Dai, Yoko Kogure, Satoshi Yamamoto, Wensheng Zhang, Koichi Noguchi. Etodolac activates and desensitizes transient receptor potential ankyrin 1. Journal of neuroscience research. 2013 Dec; 91(12):1591-8. doi: 10.1002/jnr.23274. [PMID: 24027177]
  • Marina Borges, Rivaldo Marini Filho, Cecília Braga Laposy, Priscylla Tatiana Chalfun Guimarães-Okamoto, Marina Platzeck Chaves, André Nanny Le Sueur Vieira, Alessandra Melchert. Nonsteroidal anti-inflammatory therapy: changes on renal function of healthy dogs. Acta cirurgica brasileira. 2013 Dec; 28(12):842-7. doi: 10.1590/s0102-86502013001200006. [PMID: 24316857]
  • Ahmed Abd-Elbary, Mina Ibrahim Tadros, Ahmed Adel Alaa-Eldin. Sucrose stearate-enriched lipid matrix tablets of etodolac: modulation of drug release, diffusional modeling and structure elucidation studies. AAPS PharmSciTech. 2013 Jun; 14(2):656-68. doi: 10.1208/s12249-013-9951-3. [PMID: 23572253]
  • Hiroshi Imamura, Jiro Hata, Ai Iida, Noriaki Manabe, Ken Haruma. Evaluating the effects of diclofenac sodium and etodolac on renal hemodynamics with contrast-enhanced ultrasonography: a pilot study. European journal of clinical pharmacology. 2013 Feb; 69(2):161-5. doi: 10.1007/s00228-012-1336-0. [PMID: 22732768]
  • Katsuhito Miyazawa, Yoshitaka Takahashi, Nobuyo Morita, Manabu T Moriyama, Takeo Kosaka, Matomo Nishio, Tanihiro Yoshimoto, Koji Suzuki. Cyclooxygenase 2 and prostaglandin E2 regulate the attachment of calcium oxalate crystals to renal epithelial cells. International journal of urology : official journal of the Japanese Urological Association. 2012 Oct; 19(10):936-43. doi: 10.1111/j.1442-2042.2012.03060.x. [PMID: 22640700]
  • P Mehta, M Lukacs, S M Abraham. Normal in the blood, abnormal in the urine. QJM : monthly journal of the Association of Physicians. 2012 Oct; 105(10):1001-2. doi: 10.1093/qjmed/hcr164. [PMID: 21880696]
  • Kathryn K Surdyk, Dawn L Sloan, Scott A Brown. Renal effects of carprofen and etodolac in euvolemic and volume-depleted dogs. American journal of veterinary research. 2012 Sep; 73(9):1485-90. doi: 10.2460/ajvr.73.9.1485. [PMID: 22924732]
  • Yukiko Nozawa, Ayako Sato, Hoglan Piao, Tetsuo Morioka, Ichiei Narita, Takashi Oite. The effect of renal administration of a selective cyclooxygenase-2 inhibitor or stable prostaglandin I2 analog on the progression of sclerotic glomerulonephritis in rats. Clinical and experimental nephrology. 2012 Apr; 16(2):221-30. doi: 10.1007/s10157-011-0558-2. [PMID: 22147282]
  • Ahmed Abd-Elbary, Mina Ibrahim Tadros, Ahmed Adel Alaa-Eldin. Development and in vitro/in vivo evaluation of etodolac controlled porosity osmotic pump tablets. AAPS PharmSciTech. 2011 Jun; 12(2):485-95. doi: 10.1208/s12249-011-9608-z. [PMID: 21479749]
  • Valentina L Kouznetsova, Igor F Tsigelny, Megha A Nagle, Sanjay K Nigam. Elucidation of common pharmacophores from analysis of targeted metabolites transported by the multispecific drug transporter-Organic anion transporter1 (Oat1). Bioorganic & medicinal chemistry. 2011 Jun; 19(11):3320-40. doi: 10.1016/j.bmc.2011.04.045. [PMID: 21571536]
  • Yuuki Akagi, Yuta Nio, Shuji Shimada, Takao Aoyama. Influence of nonsteroidal anti-inflammatory drugs on the antiplatelet effects of aspirin in rats. Biological & pharmaceutical bulletin. 2011; 34(2):233-7. doi: 10.1248/bpb.34.233. [PMID: 21415533]
  • Ota Fuchs. Transcription factor NF-κB inhibitors as single therapeutic agents or in combination with classical chemotherapeutic agents for the treatment of hematologic malignancies. Current molecular pharmacology. 2010 Nov; 3(3):98-122. doi: 10.2174/1874467211003030098. [PMID: 20594187]
  • J N King, C Rudaz, L Borer, M Jung, W Seewald, P Lees. In vitro and ex vivo inhibition of canine cyclooxygenase isoforms by robenacoxib: a comparative study. Research in veterinary science. 2010 Jun; 88(3):497-506. doi: 10.1016/j.rvsc.2009.11.002. [PMID: 20004922]
  • Kimihiko Yanaoka, Masashi Oka, Noriko Yoshimura, Hisanobu Deguchi, Chizu Mukoubayashi, Shotaro Enomoto, Takao Maekita, Izumi Inoue, Kazuki Ueda, Hirotoshi Utsunomiya, Mikitaka Iguchi, Hideyuki Tamai, Mitsuhiro Fujishiro, Yasushi Nakamura, Tetsuya Tsukamoto, Kenichi Inada, Tatsuya Takeshita, Masao Ichinose. Preventive effects of etodolac, a selective cyclooxygenase-2 inhibitor, on cancer development in extensive metaplastic gastritis, a Helicobacter pylori-negative precancerous lesion. International journal of cancer. 2010 Mar; 126(6):1467-73. doi: 10.1002/ijc.24862. [PMID: 19711347]
  • Nahla S Barakat. Enhanced oral bioavailability of etodolac by self-emulsifying systems: in-vitro and in-vivo evaluation. The Journal of pharmacy and pharmacology. 2010 Feb; 62(2):173-80. doi: 10.1211/jpp.62.02.0004. [PMID: 20487196]
  • Savita Vyas, Piyush Trivedi, Subhash Chandra Chaturvedi. Dextran-etodolac conjugates: synthesis, in vitro and in vivo evaluation. Acta poloniae pharmaceutica. 2009 Mar; 66(2):201-6. doi: NULL. [PMID: 19719056]
  • Marjo J Karjalainen, Pertti J Neuvonen, Janne T Backman. In vitro inhibition of CYP1A2 by model inhibitors, anti-inflammatory analgesics and female sex steroids: predictability of in vivo interactions. Basic & clinical pharmacology & toxicology. 2008 Aug; 103(2):157-65. doi: 10.1111/j.1742-7843.2008.00252.x. [PMID: 18816299]
  • Mojca Brunskole, Bogdan Stefane, Karmen Zorko, Marko Anderluh, Jure Stojan, Tea Lanisnik Rizner, Stanislav Gobec. Towards the first inhibitors of trihydroxynaphthalene reductase from Curvularia lunata: synthesis of artificial substrate, homology modelling and initial screening. Bioorganic & medicinal chemistry. 2008 Jun; 16(11):5881-9. doi: 10.1016/j.bmc.2008.04.066. [PMID: 18482840]
  • Yin-Xiu Jin, Yi-Hong Tang, Su Zeng. Analysis of flurbiprofen, ketoprofen and etodolac enantiomers by pre-column derivatization RP-HPLC and application to drug-protein binding in human plasma. Journal of pharmaceutical and biomedical analysis. 2008 Apr; 46(5):953-8. doi: 10.1016/j.jpba.2008.01.038. [PMID: 18329215]
  • Hyun-Soo Lee, Il-Mo Kang, Heon-Woo Lee, Ji-Hyung Seo, Ju-Hee Ryu, Sang-Jun Choi, Myung-Jae Lee, Seo-Young Jeong, Young-Wuk Cho, Kyung-Tae Lee. Development and validation of a high performance liquid chromatography-tandem mass spectrometry for the determination of etodolac in human plasma. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2008 Feb; 863(1):158-62. doi: 10.1016/j.jchromb.2007.11.032. [PMID: 18218344]
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