Trifluoroacetic Acid

Trifluoroacetic Acid

SCHEMBL726303

CCN(CC)CC.O=C(O)C(F)(F)F

nearest known ligand 0.36

Full drug profile on Sugi Atlas →

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MLYCD O95822 1/20 0.36
FAAH O00519 9/20 0.36
CES1 P23141 6/20 0.34
CES2 O00748 4/20 0.34
MEN1 O00255 1/20 0.34
CYP1A2 P05177 1/20 0.34
KMT2A Q03164 1/20 0.34
HSD17B10 Q99714 1/20 0.34
ARG1 P05089 2/20 0.34
ARG2 P78540 2/20 0.34
PPIP5K2 O43314 1/20 0.34
FFAR3 O14843 1/20 0.33
CHRM2 P08172 1/20 0.33
CHRM4 P08173 1/20 0.33
CHRM5 P08912 1/20 0.33
CHRM1 P11229 1/20 0.33
CHRM3 P20309 1/20 0.33

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.

Compoundsimilaritytop predictedshared targets
Trifluoroacetic Acid SCHEMBL3708678 1.00 MLYCD (0.36) MLYCDFAAHCES1CES2MEN1
Trifluoroacetic Acid SCHEMBL3708677 1.00 MLYCD (0.36) MLYCDFAAHCES1CES2MEN1
Trifluoroacetic Acid SCHEMBL29024974 0.97 MLYCD (0.35) MLYCDFAAHCES1CES2MEN1
Trifluoroacetic Acid SCHEMBL6534847 0.95 MLYCD (0.34) MLYCDFAAHCES1CES2MEN1
Trifluoroacetic Acid SCHEMBL7929496 0.95 MLYCD (0.34) MLYCDFAAHCES1CES2MEN1
Trifluoroacetic Acid SCHEMBL9293783 0.89 MLYCD (0.34) MLYCDFAAHARG1ARG2PPIP5K2
Trifluoroacetic Acid SCHEMBL6534970 0.87 FAAH (0.47) FAAHCES1CES2MEN1CYP1A2
Trifluoroacetic Acid SCHEMBL1432240 0.85 TDP1 (0.44) MLYCDFAAHMEN1CYP1A2KMT2A
Trifluoroacetic Acid SCHEMBL28455031 0.85 PPIP5K2 (0.38) MLYCDPPIP5K2
Trifluoroacetic Acid SCHEMBL17396033 0.83 CHRM2 (0.38) MLYCDFAAHCES1CES2MEN1

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 264 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110922582-B Perfluoro polyether siloxane compound and preparation method and application thereof 东莞东阳光科研发有限公司 2023-06-09 CN claimed
CN-109897176-B Perfluoropolyether siloxane compound and synthesis method and application thereof 乳源东阳光氟有限公司 2022-12-27 CN claimed
CN-115141257-A Purification method of degarelix 浙江苏泊尔制药有限公司 2022-10-04 CN claimed
CN-111393253-A Synthesis method of compound containing trans-substituted cyclohexyl 江苏广域化学有限公司 2020-07-10 CN claimed
CN-110922582-A Perfluoropolyether siloxane compound and preparation method and application thereof 东莞东阳光科研发有限公司 2020-03-27 CN claimed
CN-109897176-A A kind of perfluoropolyether silicone compounds and its synthetic method and application 乳源东阳光氟有限公司 2019-06-18 CN claimed
EP-1861364-B1 PREPARATION OF AN ATORVASTATIN INTERMEDIATE USING A PAAL-KNORR CONDENSATION C P PHARMACEUTICALS INTERNAT C V (US) 2011-05-11 EP claimed
US-7709169-B2 Charge trapping releaser containing charge transport layer photoconductors XEROX CORPORATION (US) 2010-05-04 US claimed
US-7687212-B2 Charge trapping releaser containing photogenerating layer photoconductors XEROX CORPORATION (US) 2010-03-30 US claimed
US-20090092909-A1 CHARGE TRAPPING RELEASER CONTAINING PHOTOGENERATING LAYER PHOTOCONDUCTORS XEROX CORPORATION (US) 2009-04-09 US claimed
US-20090092908-A1 CHARGE TRAPPING RELEASER CONTAINING CHARGE TRANSPORT LAYER PHOTOCONDUCTORS XEROX CORPORATION (US) 2009-04-09 US claimed
JP-2008533128-A 2008-08-21 JP claimed
EP-1861364-A1 PREPARATION OF AN ATORVASTATIN INTERMEDIATE USING A PAAL-KNORR CONDENSATION Pfizer Science and Technology Ireland Limited (IE) 2007-12-05 EP claimed
WO-2006097909-A1 PREPARATION OF AN ATORVASTATIN INTERMEDIATE USING A PAAL-KNORR CONDENSATION PFIZER SCIENCE AND TECHNOLOGY IRELAND LIMITED (IE) 2006-09-21 WO claimed
US-20050196789-A1 Preparation of biologically derived fluids for biomarker determination by mass spectrometry APPLERA CORPORATION (US) 2005-09-08 US claimed
EP-4320138-B1 PSEUDO SOLID PHASE PROTECTING GROUP AND METHODS FOR THE SYNTHESIS OF OLIGONUCLEOTIDES AND OLIGONUCLEOTIDE CONJUGATES BACHEM AG (CH) 2026-04-01 EP disclosed
US-20260062375-A1 AMINE SEPARATION METHOD DAICEL CORPORATION (JP) 2026-03-05 US disclosed
US-4386026-A Cell-specific glycopeptide ligands MERCK & CO., INC. (US) 1983-05-31 US disclosed
EP-0063373-A1 Cell-specific glycopeptide ligands MERCK & CO. INC. (US) 1982-10-27 EP disclosed
US-3944538-A Process and apparatus for the synthesis of peptides not linked to polymers BODANSZKY MIKLOS 1976-03-16 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20260062375-A1 AMINE SEPARATION METHOD SLC7A1, SAMM50, PNMT MLYCD 4671/4885FAAH 1434/4885CES1 547/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.