Trifluoroacetic Acid — predicted protein targets

Known targets — ChEMBL curated mechanism

ABCC8 ACE ADORA1 ADORA2A ADORA2B ADORA3 ALDH5A1 ALOX5 ALOX5AP ATP4A ATP4B BRAF CA1 CA12 CA2 CA4 CYSLTR1 DHFR DPEP1 EDNRA EDNRB ESR2 F10 FDPS FGF1 GABBR1 GABBR2 GABRA1 GABRA2 GABRA3 GABRA4 GABRA5 GABRA6 GABRB1 GABRB2 GABRB3 GABRD GABRE GABRG1 GABRG2 GABRG3 GABRP GABRQ GART GNRHR GSC1 HMGCR IMPDH1 IMPDH2 KCNJ11 LY96 NOD2 NR3C1 NS3 NS4A NS5b P2RY1 P2RY12 P2RY2 P2RY4 P2RY6 PBP2X PDE3A PDE3B PDE4A PDE4B PDE4C PDE4D PDK1 PDK2 PDK3 PDK4 PPARG PPAT PTGIR PTGS1 PTGS2 RAF1 RYR1 RYR3 SCN10A SCN11A SCN1A SCN2A SCN3A SCN4A SCN5A SCN7A SCN8A SCN9A SERPINC1 SLC12A1 SLC12A3 SYK THRA THRB TLR3 TLR4 TLR9 TUBA1A TUBA1B TUBA1C TUBA3C TUBA3E TUBA4A TUBB TUBB1 TUBB2A TUBB2B TUBB3 TUBB4A TUBB4B TUBB6 TUBB8 TYMS VKORC1 XDH bla blaIMP-1 blaOXA-33 blaOXA-58 blaT-3 blaT-4 blaT-5 blaT-6 dacA dacB dacC folA folP folP1 ftsI fusA gag gyrA gyrB mecA mrcA mrcB mrdA pbp1a pbp1b pbp2 pbp2a pbp2b pbp3 pbp4 pbpA pbpB pbpC pbpF pol ponB rplA rplB rplC rplD rplE rplF rplJ rplK rplL rplM rplN rplO rplP rplQ rplR rplS rplT rplU rplV rplW rplX rplY rpmA rpmB rpmC rpmD rpmE rpmF rpmG rpmH rpmI rpmJ rpoA rpoB rpoC rpoZ rpsA rpsB rpsC rpsD rpsE rpsF rpsG rpsH rpsI rpsJ rpsK rpsL rpsM rpsN rpsO rpsP rpsQ rpsR rpsS rpsT rpsU ykgM ykgO

The experimentally established mechanism targets of Trifluoroacetic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

	gene	UniProt	supporting neighbours	confidence
▸	HTR6	P50406	16/20	0.37

▸	CYP3A4	P08684	1/20	0.36

▸	HTR2A	P28223	1/20	0.36

▸	HTR2C	P28335	1/20	0.36

▸	HTR2B	P41595	1/20	0.36

▸	CACNA1B	Q00975	1/20	0.33

▸	TPSAB1	Q15661	1/20	0.32

▸	LMNA	P02545	1/20	0.31

▸	SMN1; SMN2	Q16637	1/20	0.31

▸	PKM	P14618	1/20	0.31

▸	PKLR	P30613	1/20	0.31

▸	DRD2	P14416	1/20	0.31

▸	DRD3	P35462	1/20	0.31

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compound	similarity	top predicted	shared targets
Trifluoroacetic Acid SCHEMBL1997380	0.98	HTR6 (0.38)	HTR6CYP3A4HTR2AHTR2CHTR2B
SCHEMBL2003639	0.91	HTR6 (0.42)	HTR6CYP3A4HTR2AHTR2CHTR2B
Trifluoroacetic Acid SCHEMBL1994879	0.90	KDM4E (0.36)	HTR6LMNASMN1; SMN2
Trifluoroacetic Acid SCHEMBL1998089	0.90	HTR6 (0.39)	HTR6HTR2CSMN1; SMN2PKMPKLR
Trifluoroacetic Acid SCHEMBL1998907	0.88	ALDH1A1 (0.37)	HTR6HTR2CPKMPKLRDRD3
SCHEMBL1998227	0.83	HTR6 (0.36)	HTR6CYP3A4HTR2AHTR2CHTR2B
SCHEMBL2001918	0.82	PKM (0.44)	HTR6CYP3A4HTR2CSMN1; SMN2PKM
SCHEMBL1995792	0.81	HTR6 (0.36)	HTR6CYP3A4HTR2AHTR2CHTR2B
SCHEMBL1998665	0.81	PKM (0.39)	HTR6HTR2CPKMPKLRDRD3
Trifluoroacetic Acid SCHEMBL1998224	0.80	HTR6 (0.40)	HTR6CYP3A4HTR2AHTR2CHTR2B

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 2 patents. claimed = in the patent's claims; disclosed = body only.

Patent	Title	Assignee	Published	Priority	Filing	Country	Status
EP-2091953-A1	8-SULFONYL-L, 3, 4, 8-TETRAHYDR0-2H- [1, 4]OXAZEPINO [6, 7-E]INDOLE DERIVATIVES AND THEIR USE AS 5-HT6 RECEPTOR LIGANDS	BIOVITRUM AB (publ) (SE)	2009-08-26	—	—	EP	disclosed
WO-2008054288-A1	8-SULFONYL-L, 3, 4, 8-TETRAHYDR0-2H- [1, 4] OXAZEPINO [6, 7-E] INDOLE DERIVATIVES AND THEIR USE AS 5-HT6 RECEPTOR LIGANDS	BIOVITRUM AB (PUBL) (SE)	2008-05-08	—	—	WO	disclosed