Thenoyltrifluoroacetone

Thenoyltrifluoroacetone^[1]
Names
	Preferred IUPAC name 4,4,4-Trifluoro-1-(thiophen-2-yl)butane-1,3-dione
	Other names 2-thenoyltrifluoroacetone
Identifiers
CAS Number	326-91-0 ;
3D model (JSmol)	Interactive image;
Abbreviations	TTFA
ChEMBL	ChEMBL1236433;
ChemSpider	5399 ;
DrugBank	DB04795 ;
ECHA InfoCard	100.005.743
EC Number	206-316-7;
PubChem CID	5601;
UNII	MYQ9MNW7NI ;
CompTox Dashboard (EPA)	DTXSID1059812 ;
	InChI InChI=1S/C8H5F3O2S/c9-8(10,11)7(13)4-5(12)6-2-1-3-14-6/h1-3H,4H2 Key: TXBBUSUXYMIVOS-UHFFFAOYSA-N ; InChI=1/C8H5F3O2S/c9-8(10,11)7(13)4-5(12)6-2-1-3-14-6/h1-3H,4H2 Key: TXBBUSUXYMIVOS-UHFFFAOYAR;
	SMILES O=C(c1sccc1)CC(=O)C(F)(F)F;
Properties
Chemical formula	C8H5F3O2S
Molar mass	222.18 g mol−1
Appearance	fine, slightly yellow crystals
Melting point	40 to 44 °C (104 to 111 °F; 313 to 317 K)
Boiling point	96 to 98 °C (205 to 208 °F; 369 to 371 K) 8 mmHg
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Flash point	12 °C (54 °F; 285 K) (closed cup)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Thenoyltrifluoroacetone, C₈H₅F₃O₂S, is a chemical compound used pharmacologically as a chelating agent. It is an inhibitor of cellular respiration by blocking the respiratory chain at complex II.

Perhaps the first report of TTFA as an inhibitor of respiration was by A. L. Tappel in 1960.^[2] Tappel had the (erroneous) idea that inhibitors like antimycin and alkyl hydroxyquinoline-N-oxide might work by chelating iron in the hydrophobic milieu of respiratory membrane proteins, so he tested a series of hydrophobic chelating agents. TTFA was a potent inhibitor, but not because of its chelating ability. TTFA binds at the quinone reduction site in Complex II, preventing ubiquinone from binding. The first x-ray structure of Complex II showing how TTFA binds, 1ZP0, was published in 2005 .^[3]

Thenoyltrifluoroacetone can be made in a Claisen condensation of ethyl trifluoroacetate and 2-acetylthiophene.^[4]

References edit

^ Sigma-Aldrich product page
^ Tappel (July 1960). "Inhibition of electron transport by antimycin A, alkyl hydroxy naphthoquinones and metal coordination compounds". Biochem. Pharmacol. 3 (4): 289–96. doi:10.1016/0006-2952(60)90094-0. PMID 13836892.
^ Sun, Fei; Huo, Xia; Zhai, Yujia; Wang, Aojin; Xu, Jianxing; Su, Dan; Bartlam, Mark; Rao, Zihe (2005). "Crystal Structure of Mitochondrial Respiratory Membrane Protein Complex II". Cell. 121 (7): 1043–1047. doi:10.1016/j.cell.2005.05.025. PMID 15989954. S2CID 16697879.
^ Gergel, Max G. (March 1977). Excuse me sir, would you like to buy a kilo of isopropyl bromide? (PDF). Pierce Chemical. p. 130.

This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it.

[1] Sigma-Aldrich product page

[2] Tappel (July 1960). "Inhibition of electron transport by antimycin A, alkyl hydroxy naphthoquinones and metal coordination compounds". Biochem. Pharmacol. 3 (4): 289–96. doi:10.1016/0006-2952(60)90094-0. PMID 13836892.

[3] Sun, Fei; Huo, Xia; Zhai, Yujia; Wang, Aojin; Xu, Jianxing; Su, Dan; Bartlam, Mark; Rao, Zihe (2005). "Crystal Structure of Mitochondrial Respiratory Membrane Protein Complex II". Cell. 121 (7): 1043–1047. doi:10.1016/j.cell.2005.05.025. PMID 15989954. S2CID 16697879.

[4] Gergel, Max G. (March 1977). Excuse me sir, would you like to buy a kilo of isopropyl bromide? (PDF). Pierce Chemical. p. 130.

[1]

[2]

[3]

[4]