Molecular Formula | C26H28Cl2N4O4 |
Molar Mass | 531.43 |
Density | 1.38 |
Melting Point | 146℃ |
Boling Point | 753.4±60.0 °C(Predicted) |
Specific Rotation(α) | -10.5 ° (C=0.4, CHCl3) |
Flash Point | 409.4°C |
Solubility | Insoluble in water |
Vapor Presure | 1.39E-22mmHg at 25°C |
Appearance | White crystalline powder |
pKa | 6.88±0.12(Predicted) |
Storage Condition | 2-8℃ |
Sensitive | Sensitive to heat |
Refractive Index | 1.642 |
MDL | MFCD00058579 |
Physical and Chemical Properties | Melting Point: 146°C |
Use | For antifungal drugs, used to treat beriberi and dandruff and other conditions |
Hazard Symbols | T - Toxic |
Risk Codes | R25 - Toxic if swallowed |
Safety Description | S36 - Wear suitable protective clothing. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
UN IDs | UN 2811 |
Reference Show more | 1. Zhou Guojian, Ye Dongting, Deng Xuxing. Effects of yinhuang granule, Niuhuang Shangqing pill and Shuanghuanglian mixture on activity of drug metabolizing enzyme cyp3a_4 [J]. Asia-Pacific Traditional Medicine, 2016,12(15):19-22. 2. Zhou Guojian, Ye Dongting, Deng Xuxing. Effects of Huanglian Shangqing pills, Hugan Pian and Niuhuang Jiedu pills on activity of drug metabolizing enzyme CYP3A4 [J]. Chinese national and folk medicine, 2016, 10(v.25;No.279):22-24. 3. Zhou Guojian, Ye Dongting, Deng Xuxing. Effects of Banlangen granules, Yinzhihuang granules and compound berberine tablets on activity of drug metabolizing enzyme cyp3a_4 [J]. Chinese Medicine Review, 2017,23(03):72-74. 4. Zhong Jing, zuoxiaoting, Wang Xiaoqin, et al. Study on the induction of four active components of licorice [J]. Journal of Shihezi University: natural science edition, 2016, 34(004):468-472. 5. Peng Yan, Yang Chao, Jiang Yaozhang, etc. Isolation and identification of fine-pole Streptomyces from beef cattle [J]. Chinese Journal of Preventive Veterinary Medicine, 2020, v.42(01):86-89 99. 6. Ma Xiaoping, Yang Qiuxia, Yu cast, etc. Comparison of some biological characteristics and drug sensitivity test between wild strain (Z20) and mutant strain (Zt) of Cladosporium from giant panda [J]. Journal of Agricultural Sciences of Zhejiang, 2018(8):1328-1335. 7. Wang Chengyu, Li Dengke, Quan Zhengyang, Hu Ying also, Sun Zhenxiao. Study on hepatotoxicity and related components of Polygonum multiflorum based on cytochrome oxidase CYP2D6 [J]. Pharmacovigilance in China, 2021,18(03):220-227 239. 8. Chen Rui, Zhou Wei, Zhang Li, Zhu Gaogao, Huang Jing, Tang Lei. In vitro inhibition of five common Cytochrome P_(450) enzymes in human liver microsomes by bevacizumab acid A [J]. China Pharmacy, 2021,32(02):195-200. 9. Huang, Wei, et al. "Effects of osthol on activity, mRNA and protein expression of Cyp3a in rats in vivo." Biopharmaceutics & drug disposition 41.1-2 (2020): 64-71.https://doi.org/10.1002/bdd.2214 10. Huang, Wei, et al. "Effects of osthol on activity, mRNA and protein expression of Cyp3a in rats in vivo." Biopharmaceutics & drug disposition 41.1-2 (2020): 64-71.https://doi.org/10.1002/bdd.2214 11. [IF=4.411] Xu Zhang et al."In Vitro and In Situ Characterization of the Intestinal Absorption of Capilliposide B and Capilliposide C from Lysimachia capillipes Hemsl."Molecules. 2019 Jan;24(7):1227 12. [IF=5.076] Liu Zi-Jing et al."The Alexipharmic Mechanisms of Five Licorice Ingredients Involved in CYP450 and Nrf2 Pathways in Paraquat-Induced Mice Acute Lung Injury."Oxid Med Cell Longev. 2019;2019:7283104 13. [IF=1.663] Wei Huang et al."Effects of osthol on activity, mRNA and protein expression of Cyp3a in rats in vivo."Biopharm Drug Dispos. 2020 Feb;41(1-2):64-71 14. [IF=3.5] Ying-huan Hu et al."Inhibition of CYP3A4 enhances aloe-emodin induced hepatocyte injury."Toxicol In Vitro. 2021 Dec;:105276 |
white crystalline powder. Melting Point 146 °c.
A mixture of 1-acetyl-4-(4-hydroxybenzene) piperazine, sodium cyanide, dimethyl sulfate and benzene was stirred at 40 °c for 1H, then 2-(2.4 monodichlorobenzene) was added -2-(1H-imidazole-1-ylmethyl)-1, 3-oxopentylcyclo-4-ylmethyl methanesulfonate, stirred at 100 ° C. For a certain time. The reaction product was post-treated to obtain ketoconazole.
imidazole antifungal drugs can inhibit the biosynthesis of ergosterol in fungal cell membrane, affect the permeability of cell membrane and inhibit its growth. Can be used for the treatment of superficial and deep mycosis, such as skin and onychomycosis, vaginal candidiasis, gastrointestinal fungal infections, etc., as well as by Candida albicans, Coccidioides, systemic infection caused by histoplasmosis.
mouse, rat, guinea pig, dog LDso(mg/kg): 44, 86, 28, 49 intravenous injection; 702, 227, 202, 780 oral.