Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Moligand™, ≥98%(HPLC) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 38 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
This product is white, odorless and slightly bitter. This product is soluble in ethanol or chloroform, slightly soluble in boiling water and slightly soluble in glycerol. Solubility: 1g/1310ml cold water, 1g/82ml, 1g/15ml cold ethanol, 1g/2.8ml boiling ethanol, 1g/14ml chloroform, 1g/90ml ether. Substrates of CYP1A2 and CYP2D6.
| ALogP | 1.6 |
|---|
| Pubchem Sid | 504750805 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504750805 |
| Sonrisas canónicas | CCOC1=CC=C(C=C1)NC(=O)C |
| IUPAC Name | N-(4-ethoxyphenyl)acetamide |
| InChIKey | CPJSUEIXXCENMM-UHFFFAOYSA-N |
| INCHI | 1S/C10H13NO2/c1-3-13-10-6-4-9(5-7-10)11-8(2)12/h4-7H,3H2,1-2H3,(H,11,12) |
| Isómeros SMILES | CCOC1=CC=C(C=C1)NC(=O)C |
| WGK Alemania | 3 |
| RTECS | AM4375000 |
| Peso molecular | 179.22 |
| Beilstein | 1869238 |
| Reaxy-Rn | 1869238 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1869238&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Anilides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acetanilides |
| Alternative Parents | N-acetylarylamines Phenoxy compounds Phenol ethers Alkyl aryl ethers Acetamides Secondary carboxylic acid amides Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Acetanilide - N-acetylarylamine - Phenoxy compound - Phenol ether - N-arylamide - Alkyl aryl ether - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Ether - Carboxylic acid derivative - Organic oxygen compound - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as acetanilides. These are organic compounds containing an acetamide group conjugated to a phenyl group. |
| External Descriptors | aromatic ether - acetamides |
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Mar 04, 2025 | P109420 | |
| Certificate of Analysis | Mar 04, 2025 | P109420 | |
| Certificate of Analysis | Jul 27, 2024 | P109420 | |
| Certificate of Analysis | Jul 27, 2024 | P109420 | |
| Certificate of Analysis | Jul 27, 2024 | P109420 | |
| Certificate of Analysis | Jul 27, 2024 | P109420 | |
| Certificate of Analysis | Jul 27, 2024 | P109420 | |
| Certificate of Analysis | Jun 09, 2021 | P109420 | |
| Certificate of Analysis | Jun 09, 2021 | P109420 | |
| Certificate of Analysis | May 06, 2021 | P109420 | |
| Certificate of Analysis | May 06, 2021 | P109420 | |
| Certificate of Analysis | May 06, 2021 | P109420 | |
| Certificate of Analysis | May 06, 2021 | P109420 |
| Solubilidad | DMSO : ≥ 100 mg/mL;H2O : 0.67 mg/m |
|---|---|
| Índice de refracción | 1.51 |
| Punto de ebullición (°C) | 132°C/4mmHg |
| Punto de fusión (°C) | 133-136°C |
| Peso molecular | 179.220 g/mol |
| XLogP3 | 1.600 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 179.095 Da |
| Monoisotopic Mass | 179.095 Da |
| Topological Polar Surface Area | 38.300 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 162.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Sainan Wang, Chao Yuan, Wei Chen, Yifan Niu, Yexi Yan, Fan Li, Hongmei Jiang. (2023) 3D spherical CuO@g-C3N4 composites activating peroxymonosulfate for high efficient degradation of 2,4,6-trichlorophenol: The mechanism of 1O2 generation. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2023.148050] |
| 2. Shisi Deng, Zezhong Shan, Qianqian Wei, Wei Li, Jing Guo, Cheng Chen, Ying Li. (2023) Amorphous zirconium phosphate as a recycled material anchored cobalt for catalytic degradation of phenacetin via peroxymonosulfate activation. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2023.125630] |
| 3. Minjie Peng, Yufeng Sun, Wen Zang, Changyong Gao, Lijing Miao, Aiguo Wu, Yujie Zhang. (2023) A highly sensitive method for the detection of p-Aminophenol based on Cu–Au nanoparticles and KIO3. ANALYTICA CHIMICA ACTA, [PMID:37977800] [10.1016/j.aca.2023.341954] |
| 4. Fang Fang, Shaohua Zhang, Chaofan Chen, Xueying Wang, Chuannan Luo, Qin Wei. (2023) A fluorescent nanoprobe based on N/S co-doped carbon dots coupled with molecularly imprinted polymers for the detection of curcumin. OPTICAL MATERIALS, [PMID:] [10.1016/j.optmat.2023.113800] |
| 5. Xiaofei Xin, Jingjing Li, Wantao Wu, Pengbo Zhao, Yang Yang, Ying Zhu, Lianjie Ren, Chao Qin, Lifang Yin. (2023) ROS-scavenging nanomedicine for “multiple crosstalk” modulation in non-alcoholic fatty liver disease. Biomaterials Science, 11 (10): (3709-3725). [PMID:37039546] [10.1039/D2BM02161G] |
| 6. Dongli Qi, Huihui Li, Chunxia Liang, Peijin Peng, Zhen Yang, Yanquan Gao, Ziwei Li, Qingqing Zhang, Zhidong Liu. (2023) Herb-drug interaction of Xingnaojing injection and Edaravone via pharmacokinetics, mixed inhibition of UGTs, and molecular docking. PHYTOMEDICINE, [PMID:36764095] [10.1016/j.phymed.2023.154696] |
| 7. Li Yingzi, Liu Xiaoyan, Li Ludi, Zhang Tao, Gao Yadong, Zeng Kewu, Wang Qi. (2023) Characterization of the metabolism of eupalinolide A and B by carboxylesterase and cytochrome P450 in human liver microsomes. Frontiers in Pharmacology, [PMID:36762117] [10.3389/fphar.2023.1093696] |
| 8. Shiqi Duan, Yan Jia, Zhihang Zhu, Lancheng Wang, Peng Xu, Youmei Wang, Bin Di, Chi Hu. (2022) Induction of CYP450 by illicit drugs: Studies using an in vitro 3D spheroidal model in comparison to animals. TOXICOLOGY LETTERS, [PMID:35914676] [10.1016/j.toxlet.2022.07.815] |
| 9. Zeming Wang, Li Liu, Yeqing Lan, Wei Li. (2022) Sn0-modified carbon derived from cigarette butts as a recycled material for enhanced removal of antibiotic phenacetin. Journal of Environmental Chemical Engineering, [PMID:] [10.1016/j.jece.2022.107164] |
| 10. Li Liu, Yuxin Li, Wei Li, Yeqing Lan, Ying Li. (2021) CrPO4 as a recycled material supported Co3O4 as an efficient peroxymonosulfate catalyst for phenacetin elimination from aqueous solution. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2021.133558] |
| 11. Bei Tan, Jie Chen, Siyuan Qin, Chuyao Liao, Ying Zhang, Di Wang, Siqi Li, Zunjian Zhang, Pei Zhang, Fengguo Xu. (2021) Tryptophan Pathway-Targeted Metabolomics Study on the Mechanism and Intervention of Cisplatin-Induced Acute Kidney Injury in Rats. CHEMICAL RESEARCH IN TOXICOLOGY, [PMID:34110802] [10.1021/acs.chemrestox.1c00110] |
| 12. Zifei Qin, Peile Wang, Shuyi Duan, Xiaoying Wan, Han Xing, Jing Yang, Xiaojian Zhang, Zhihong Yao, Xinsheng Yao. (2021) Potential Determinants for Metabolic Fates and Inhibitory Effects of Isobavachalcone Involving in Human Cytochrome P450, UDP-Glucuronosyltransferase Enzymes, and Efflux Transporters. JOURNAL OF PHARMACEUTICAL SCIENCES, [PMID:33610566] [10.1016/j.xphs.2021.02.013] |
| 13. Hongfang Li, Yunyan Tang, Yang Wang, Weipeng Wei, Chengchen Yin, Fushang Tang. (2020) Effects of Saikosaponin D on CYP1A2 and CYP2D6 in HepaRG Cells. Drug Design Development and Therapy, [PMID:33273809] [10.2147/DDDT.S268358] |
| 14. Cui-Mei Liu, Hong-Yuan He, Lin Xu, Zhen-Dong Hua. (2020) New qualitative analysis strategy for illicit drugs using Raman spectroscopy and characteristic peaks method. Drug Testing and Analysis, 13 (3): (720-728). [PMID:33142047] [10.1002/dta.2963] |
| 15. Chaoqun Tan, Xinchi Jian, Haotian Wu, Tianyu Sheng, Kechun Sun, Haiying Gao. (2020) Kinetics degradation of phenacetin by solar activated persulfate system. SEPARATION AND PURIFICATION TECHNOLOGY, [PMID:] [10.1016/j.seppur.2020.117851] |
| 16. Xinqiang Li, Han Xing, Zifei Qin, Jing Yang, Peile Wang, Xiaojian Zhang, Zhihong Yao, Xinsheng Yao. (2020) Potential metabolism determinants and drug–drug interactions of a natural flavanone bavachinin. RSC Advances, 10 (58): (35141-35152). [PMID:35515695] [10.1039/D0RA06961B] |
| 17. Xing Han, Yang Jing, Ren Kaidi, Qin Zifei, Wang Peile, Zhang Xiaojian, Yao Zhihong, Gonzalez Frank J, Yao Xinsheng. (2020) Investigation on the metabolic characteristics of isobavachin in Psoralea corylifolia L. (Bu-gu-zhi) and its potential inhibition against human cytochrome P450s and UDP-glucuronosyltransferases. JOURNAL OF PHARMACY AND PHARMACOLOGY, 72 (12): (1865-1878). [PMID:32750744] [10.1111/jphp.13337] |
| 18. Qin Zifei, Jia Mengmeng, Yang Jing, Xing Han, Yin Zhao, Yao Zhihong, Zhang Xiaojian, Yao Xinsheng. (2020) Multiple circulating alkaloids and saponins from intravenous Kang-Ai injection inhibit human cytochrome P450 and UDP-glucuronosyltransferase isozymes: potential drug–drug interactions. Chinese Medicine, 15 (1): (1-18). [PMID:32655683] [10.1186/s13020-020-00349-3] |
| 19. Chaoqun Tan, Xinxin Cui, Kecun Sun, Huiming Xiang, Erdeng Du, Ling Deng, Haiying Gao. (2020) Kinetic mechanism of ozone activated peroxymonosulfate system for enhanced removal of anti-inflammatory drugs. SCIENCE OF THE TOTAL ENVIRONMENT, [PMID:32446064] [10.1016/j.scitotenv.2020.139250] |
| 20. Nana Long, Huaqiao Tang, Lin Lin, Jianlong Li, Lijuan Guo, Fenghui Sun, Min Dai. (2019) Effects of infection of MRSA on the expression and activity of renal cytochrome P450s in mice. JOURNAL OF TOXICOLOGICAL SCIENCES, [PMID:30944282] [10.2131/jts.44.299] |
| 21. Bin Xie, Yuan-Yuan Lu, Zhuo-Hui Luo, Zhao Qu, Chun-Ge Zheng, Xin-An Huang, Hong-Yan Zhou, Ying-Jie Hu, Xiao-Ling Shen. (2019) Tenacigenin B ester derivatives from Marsdenia tenacissima actively inhibited CYP3A4 and enhanced in vivo antitumor activity of paclitaxel. JOURNAL OF ETHNOPHARMACOLOGY, [PMID:30772481] [10.1016/j.jep.2019.02.028] |
| 22. Huaqiao Tang, Nana Long, Min Dai, Lin Lin, Jianlong Li, Fenghui Sun, Lijuan Guo. (2018) Effect of citral on mouse hepatic cytochrome P450 enzymes. PHARMACEUTICAL BIOLOGY, [PMID:29969356] [10.1080/13880209.2018.1470191] |
| 23. Xue Cai-fu, Zhang Zhe, Jin Yan, Zhu Bin, Xing Jun-fen, Ma Guo, Xiang Xiao-qiang, Cai Wei-min. (2018) Novel in vitro dynamic metabolic system for predicting the human pharmacokinetics of tolbutamide. ACTA PHARMACOLOGICA SINICA, 39 (9): (1522-1532). [PMID:29644999] [10.1038/aps.2017.201] |
| 24. Zifei Qin, Shishi Li, Zhihong Yao, Xiaodan Hong, Jinjin Xu, Pei Lin, Guoping Zhao, Frank J. Gonzalez, Xinsheng Yao. (2018) Metabolic profiling of corylin in vivo and in vitro. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, [PMID:29631076] [10.1016/j.jpba.2018.03.047] |
| 25. Xiao-qian Xu, Ting Geng, She-bing Zhang, Dan-yu Kang, Yan-jing Li, Gang Ding, Wen-zhe Huang, Zhen-zhong Wang, Wei Xiao. (2016) Inhibition of Re Du Ning Injection on Enzyme Activities of Rat Liver Microsomes Using Cocktail Method. Chinese Herbal Medicines, [PMID:] [10.1016/S1674-6384(16)60045-X] |
| 26. Junlang Qiu, Guosheng Chen, Fang Zhu, Gangfeng Ouyang. (2016) Sulfonated nanoparticles doped electrospun fibers with bioinspired polynorepinephrine sheath for in vivo solid-phase microextraction of pharmaceuticals in fish and vegetable. JOURNAL OF CHROMATOGRAPHY A, [PMID:27295966] [10.1016/j.chroma.2016.05.082] |
| 27. Huimin Duan, Leilei Li, Xiaojiao Wang, Yanhui Wang, Jianbo Li, Chuannan Luo. (2015) CdTe quantum dots@luminol for trace-level chemiluminescence sensing of phenacetin based on biological recognition materials. NEW JOURNAL OF CHEMISTRY, 40 (1): (458-463). [PMID:] [10.1039/C5NJ01305D] |
| 28. Ting Geng, Haihong Si, Danyu Kang, Yanjing Li, Wenzhe Huang, Gang Ding, Zhenzhong Wang, Yu’an Bi, Hong Zhang, Wei Xiao. (2015) Influences of Re Du Ning Injection, a traditional Chinese medicine injection, on the CYP450 activities in rats using a cocktail method. JOURNAL OF ETHNOPHARMACOLOGY, [PMID:26318744] [10.1016/j.jep.2015.08.035] |
| 29. Danyi Lu, Zhiguo Ma, Tianpeng Zhang, Xingwang Zhang, Baojian Wu. (2015) Metabolism of the anthelmintic drug niclosamide by cytochrome P450 enzymes and UDP-glucuronosyltransferases: metabolite elucidation and main contributions from CYP1A2 and UGT1A1. XENOBIOTICA, [PMID:26068521] [10.3109/00498254.2015.1047812] |
| 30. Dongmei Cui, Li Mi, Xuan Xu, Jusheng Lu, Jing Qian, Songqin Liu. (2014) Nanocomposites of Graphene and Cytochrome P450 2D6 Isozyme for Electrochemical-Driven Tramadol Metabolism. LANGMUIR, [PMID:25222611] [10.1021/la502699m] |
| 31. Qiao Xue, Ji Shuai, Yu Si-wang, Lin Xiong-hao, Jin Hong-wei, Duan Yao-kai, Zhang Liang-ren, Guo De-an, Ye Min. (2013) Identification of Key Licorice Constituents Which Interact with Cytochrome P450: Evaluation by LC/MS/MS Cocktail Assay and Metabolic Profiling. AAPS Journal, 16 (1): (101-113). [PMID:24254844] [10.1208/s12248-013-9544-9] |
| 32. Wu Xing, Yi Jian-Min, Liu Yue-Jin, Liu Yong-Bing, Zhang Pan-Liang. (2013) Solubility and micronisation of phenacetin in supercritical carbon dioxide. CHEMICAL PAPERS, 67 (5): (517-525). [PMID:] [10.2478/s11696-013-0328-6] |
| 33. Han Zhang, Fang Fang, Jiangle Yi, Yuanling Sun, Xueying Wang. (2025) Molecularly imprinted polymer coupled with zinc-doped carbon quantum dots as a fluorescent probe for the determination of doxorubicin hydrochloride. NEW JOURNAL OF CHEMISTRY, 49 (8): (3200-3206). [PMID:] [10.1039/D4NJ05142D] |
| 34. Zhiyong Wu, Xinhao Wang, Lin Wang, Na Sun, Zihui Yang, Jianguo Zeng. (2025) Research on the metabolites and key metabolic enzymes of allocryptopine in chicken liver microsomes via stable isotope tracing technology. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, [PMID:39805195] [10.1016/j.jpba.2025.116667] |
| 35. Zhang Meng, Du Pengfei, Xiao Yirong, Liu Hao, Wang Meixue, Zhang Yumei, Chen Xin. (2024) Sex differences in CYP450-based sodium dehydroacetate metabolism and its metabolites in rats. npj Science of Food, 8 (1): (1-12). [PMID:39719445] [10.1038/s41538-024-00361-z] |
| 36. Kun Peng, Qiqin Wang, Weijia Chen, Donghai Xia, Zhengyin Zhou, Yuqiang Wang, Zhengjin Jiang, Fuhai Wu. (2016) Phosphatidic acid-functionalized monolithic stationary phase for reversed-phase/cation-exchange mixed mode chromatography. RSC Advances, 6 (103): (100891-100898). [PMID:] [10.1039/C6RA21504A] |
| 37. Lifeng Niu, Lina Ding, Chunyun Lu, Feifei Zuo, Ke Yao, Shaobo Xu, Wen Li, Donghua Yang, Xia Xu. (2016) Flavokawain A inhibits Cytochrome P450 in in vitro metabolic and inhibitory investigations. JOURNAL OF ETHNOPHARMACOLOGY, [PMID:27318274] [10.1016/j.jep.2016.06.039] |
| 38. Qing-Xuan Xie, Xiao-Na Zeng, Yun-Hui Wang, Li-Xia Tan, Miao Yang, Yin-Xiao Du, Xiao-Ping Chen. (2026) Gut microbiota influence pharmacokinetics variability in aging mice: Effects vary from drug to drug. DRUG METABOLISM AND DISPOSITION, [PMID:41687425] [10.1016/j.dmd.2026.100241] |
Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →