27220-47-9 Usage
Chemical Properties
White or almost white powder
Uses
Different sources of media describe the Uses of 27220-47-9 differently. You can refer to the following data:
1. antineoplastic, anti-estrogen.
Econazole (Spectazole) is a synthetic imidazole. Econazole blocks C-14 demethylation of sterols, interfering with the biosynthesis of ergosterol, which results in disorganization of the fungal plasma cell membrane and increased permeability. It is active against dermatophytes, yeast, P. orbiculare, Aspergillus, Cladosporium, and Sporothrix.
2. Econazole (cas# 27220-47-9) is a compound useful in organic synthesis.
Indications
Econazole (Spectazole) is a synthetic imidazole. Econazole blocks C-14
demethylation of sterols, interfering with the biosynthesis of ergosterol,
which results in disorganization of the fungal plasma cell membrane and
increased permeability. It is active against dermatophytes, yeast, P. orbiculare,
Aspergillus, Cladosporium, and Sporothrix.
Therapeutic Function
Antifungal
Synthesis
Econazole, 1-[2,4-dichloro-β-[(4-chlorobenzyl)oxy]phenethyl]-imidazole
(35.2.8), is an analog of myconazole. It differs in the presence of a single chlorine atom in
the benzyl part of the molecule, and it is synthesized in the same manner, except that it
uses 4-chlorobenzylchloride in the last stage instead of 2,4-dichlorobenzylbromide.
Check Digit Verification of cas no
The CAS Registry Mumber 27220-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,2 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27220-47:
(7*2)+(6*7)+(5*2)+(4*2)+(3*0)+(2*4)+(1*7)=89
89 % 10 = 9
So 27220-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H15Cl3N2O/c19-13-3-1-12(2-4-13)10-24-18(8-15-9-22-11-23-15)16-6-5-14(20)7-17(16)21/h1-7,9,11,15,18H,8,10H2
27220-47-9Relevant articles and documents
Investigation of multi-target-directed ligands (MTDLs) with butyrylcholinesterase (BuChE) and indoleamine 2,3-dioxygenase 1 (IDO1) inhibition: The design, synthesis of miconazole analogues targeting Alzheimer's disease
Lu, Xin,He, Si-yu,Li, Qi,Yang, Hongyu,Jiang, Xueyang,Lin, Hongzhi,Chen, Yao,Qu, Wei,Feng, Feng,Bian, Yaoyao,Zhou, You,Sun, Haopeng
, p. 1665 - 1674 (2018/02/23)
In our endeavor towards the development of potent multi-target ligands for the treatment of Alzheimer's disease, miconazole was identified to show BuChE-IDO1 dual-target inhibitory effects. Morris water maze test indicated that miconazole obviously ameliorated the cognitive function impaired by scopolamine. Furthermore, it showed good safety in primary hepatotoxicity evaluation. Based on these results, we designed, synthesized, and evaluated a series of miconazole derivatives as BuChE-IDO1 dual-target inhibitors. Out of the 12 compounds, 5i and 5j exhibited the best potency in enzymatic evaluation, thus were selected for subsequent behavioral study, in which the two compounds exerted much improved effect than tacrine. Meanwhile, 5i and 5j displayed no apparent hepatotoxicity. The results suggest that miconazole analogue offers an attractive starting point for further development of new BuChE-IDO1 dual-target inhibitors against Alzheimer's disease.
