Albaconazole

Albaconazole
Clinical data
ATC code	none;
Identifiers
	IUPAC name 7-Chloro-3-[(2R,3R)-3-(2,4-difluorophenyl)-3-hydroxy-4-(1,2,4-triazol-1-yl)butan-2-yl]quinazolin-4-one;
CAS Number	187949-02-6 ;
PubChem CID	208952;
ChemSpider	181045 ;
UNII	YDW24Y8IAB;
KEGG	D09702 ;
ChEMBL	ChEMBL298817 ;
CompTox Dashboard (EPA)	DTXSID3058244 ;
ECHA InfoCard	100.170.829
Chemical and physical data
Formula	C20H16ClF2N5O2
Molar mass	431.823146 g/mol g·mol−1
3D model (JSmol)	Interactive image;
	SMILES Fc1ccc(c(F)c1)[C@](O)([C@H](N3\C=N/c2cc(Cl)ccc2C3=O)C)Cn4ncnc4;
	InChI InChI=1S/C20H16ClF2N5O2/c1-12(28-11-25-18-6-13(21)2-4-15(18)19(28)29)20(30,8-27-10-24-9-26-27)16-5-3-14(22)7-17(16)23/h2-7,9-12,30H,8H2,1H3/t12-,20-/m1/s1 ; Key:UHIXWHUVLCAJQL-MPBGBICISA-N ;
(verify)

Albaconazole (development code UR-9825) is an experimental triazole antifungal.[1] It has potential broad-spectrum activity and exhibits inhibition of numerous CYP450 hepatic enzymes.

It has also been studied as an antiprotozoal agent.[2]

References

"Albaconazole". Adis Insight.
Guedes, P. M. d. M.; Urbina, J. A.; De Lana, M.; Afonso, L. C. C.; Veloso, V. M.; Tafuri, W. L.; Machado-Coelho, G. L. L.; Chiari, E.; Bahia, M. T. (2004). "Activity of the New Triazole Derivative Albaconazole against Trypanosoma (Schizotrypanum) cruzi in Dog Hosts". Antimicrobial Agents and Chemotherapy. 48 (11): 4286–4292. doi:10.1128/AAC.48.11.4286-4292.2004. PMC 525424.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] "Albaconazole". Adis Insight.

[2] Guedes, P. M. d. M.; Urbina, J. A.; De Lana, M.; Afonso, L. C. C.; Veloso, V. M.; Tafuri, W. L.; Machado-Coelho, G. L. L.; Chiari, E.; Bahia, M. T. (2004). "Activity of the New Triazole Derivative Albaconazole against Trypanosoma (Schizotrypanum) cruzi in Dog Hosts". Antimicrobial Agents and Chemotherapy. 48 (11): 4286–4292. doi:10.1128/AAC.48.11.4286-4292.2004. PMC 525424.