Halofuginone

Halofuginone
Clinical data
Trade names	Halocur
AHFS/Drugs.com	International Drug Names
ATCvet code	QP51BX01 (WHO) ;
Legal status
Legal status	EU: Rx-only;
Identifiers
	IUPAC name 7-Bromo-6-chloro-3-[3-[(2S,3R)-3-hydroxy-2-piperidinyl]-2-oxopropyl]-4-quinazolinone;
CAS Number	55837-20-2 ;
PubChem CID	400772;
ChemSpider	355164 ;
UNII	L31MM1385E;
ChEMBL	ChEMBL1199540 ;
CompTox Dashboard (EPA)	DTXSID0048260 ;
Chemical and physical data
Formula	C16H17BrClN3O3
Molar mass	414.68 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES O=C(CN3C=NC2=CC(Br)=C(Cl)C=C2C3=O)C[C@@H]1NCCC[C@H]1O;
	InChI InChI=1S/C16H17BrClN3O3/c17-11-6-13-10(5-12(11)18)16(24)21(8-20-13)7-9(22)4-14-15(23)2-1-3-19-14/h5-6,8,14-15,19,23H,1-4,7H2/t14-,15+/m0/s1 ; Key:LVASCWIMLIKXLA-LSDHHAIUSA-N ;
	(what is this?) (verify)

Halofuginone, sold under the brand name Halocur, is a coccidiostat used in veterinary medicine. It is a synthetic halogenated derivative of febrifugine, a natural quinazolinone alkaloid which can be found in the Chinese herb Dichroa febrifuga (Chang Shan).^[3] Collgard Biopharmaceuticals is developing halofuginone for the treatment of scleroderma and it has received orphan drug designation from the U.S. Food and Drug Administration.^[4]

Halofuginone inhibits the development of T helper 17 cells, immune cells that play an important role in autoimmune disease, but it does not affect other kinds of T cells which are involved in normal immune function.^[5] Halofuginone therefore has potential for the treatment of autoimmune disorders.^[5]

Halofuginone is also an inhibitor of collagen type I gene expression and as a consequence it may inhibit tumor cell growth.^[3] Halofuginone exerts its effects by acting as a high affinity inhibitor of the enzyme glutamyl-prolyl tRNA synthetase. Inhibition of prolyl tRNA charging leads to the accumulation of uncharged prolyl tRNAs, which serve as a signal to initiate the amino acid starvation response, which in turn exerts anti-inflammatory and anti-fibrotic effects.^[6]

References

^ "Halocur EPAR". European Medicines Agency (EMA). 29 October 1999. Retrieved 26 December 2024.
^ "Halocur PI". Union Register of medicinal products. 9 November 1999. Retrieved 26 December 2024.
^ ^a ^b "Halofuginone hydrobromide". NCI Drug Dictionary. National Cancer Institute, National Institutes of Health, U.S. Department of Health and Human Services.
^ "Halofuginone Receives FDA Orphan Drug Status For Scleroderma". WebCite. 10 March 2000. Archived from the original on 4 March 2012.
^ ^a ^b Sundrud MS, Koralov SB, Feuerer M, Calado DP, Kozhaya AE, Rhule-Smith A, et al. (June 2009). "Halofuginone inhibits TH17 cell differentiation by activating the amino acid starvation response". Science. 324 (5932): 1334–8. Bibcode:2009Sci...324.1334S. doi:10.1126/science.1172638. PMC 2803727. PMID 19498172.{{cite journal}}: CS1 maint: overridden setting (link)
^ Keller TL, Zocco D, Sundrud MS, Hendrick M, Edenius M, Yum J, et al. (February 2012). "Halofuginone and other febrifugine derivatives inhibit prolyl-tRNA synthetase". Nature Chemical Biology. 8 (3): 311–7. doi:10.1038/nchembio.790. PMC 3281520. PMID 22327401.{{cite journal}}: CS1 maint: overridden setting (link)

[1] "Halocur EPAR". European Medicines Agency (EMA). 29 October 1999. Retrieved 26 December 2024.

[2] "Halocur PI". Union Register of medicinal products. 9 November 1999. Retrieved 26 December 2024.

[drugdictionary-3] "Halofuginone hydrobromide". NCI Drug Dictionary. National Cancer Institute, National Institutes of Health, U.S. Department of Health and Human Services.

[4] "Halofuginone Receives FDA Orphan Drug Status For Scleroderma". WebCite. 10 March 2000. Archived from the original on 4 March 2012.

[:0-5] Sundrud MS, Koralov SB, Feuerer M, Calado DP, Kozhaya AE, Rhule-Smith A, et al. (June 2009). "Halofuginone inhibits TH17 cell differentiation by activating the amino acid starvation response". Science. 324 (5932): 1334–8. Bibcode:2009Sci...324.1334S. doi:10.1126/science.1172638. PMC 2803727. PMID 19498172.{{cite journal}}: CS1 maint: overridden setting (link)

[6] Keller TL, Zocco D, Sundrud MS, Hendrick M, Edenius M, Yum J, et al. (February 2012). "Halofuginone and other febrifugine derivatives inhibit prolyl-tRNA synthetase". Nature Chemical Biology. 8 (3): 311–7. doi:10.1038/nchembio.790. PMC 3281520. PMID 22327401.{{cite journal}}: CS1 maint: overridden setting (link)

[1]

[2]

[3]

[4]

[5]

[6]