Trifluoroacetic Acid

Trifluoroacetic Acid

SCHEMBL332728

O=C(O)C(F)(F)F.O=S(=O)(O)O

nearest known ligand 0.58

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CALCRLCHRM1CHRM2CHRM3F2RMAOAMAOBMAP2K1MAP2K2NTRK1NTRK2NTRK3OPRD1OPRK1OPRM1P2RY12PKLRSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASLC18A2SLC6A2SLC6A3TLR7TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8dacAdacBdacCfolAftsImrcAmrcBmrdApolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmB1rpmB2rpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmHrpmIrpmJrpmJ2rpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsR1rpsR2rpsSrpsTrpsUrpsZykgMykgO

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 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.58
L3MBTL1 Q9Y468 1/20 0.58
CA5A P35218 1/20 0.43
CA5B Q9Y2D0 1/20 0.43
TSHR P16473 3/20 0.38
TDP1 Q9NUW8 1/20 0.38
THRB P10828 1/20 0.35
CA2 P00918 5/20 0.33
POLB P06746 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
TP53 P04637 1/20 0.33
MEN1 O00255 1/20 0.32
KMT2A Q03164 1/20 0.32
CES1 P23141 1/20 0.32
CA1 P00915 4/20 0.32
CA7 P43166 1/20 0.32
CA13 Q8N1Q1 1/20 0.32
ACLY P53396 2/20 0.31
CA12 O43570 2/20 0.31
CA9 Q16790 2/20 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.

Compoundsimilaritytop predictedshared targets
Trifluoroacetic Acid SCHEMBL19856417 0.97 ALDH1A1 (0.55) ALDH1A1L3MBTL1CA5ACA5BTSHR
Trifluoroacetic Acid SCHEMBL529369 0.91 ALDH1A1 (0.50) ALDH1A1L3MBTL1CA5ACA5BTSHR
Trifluoroacetic Acid SCHEMBL10510205 0.90 ALDH1A1 (0.55) ALDH1A1L3MBTL1CA5ACA5BTSHR
Trifluoromethanesulfonic Acid SCHEMBL991785 0.87 ALDH1A1 (0.60) ALDH1A1L3MBTL1TSHRTDP1THRB
Trifluoroacetic Acid SCHEMBL144167 0.87 ALDH1A1 (0.52) ALDH1A1L3MBTL1CA5ACA5BTSHR
Trifluoroacetic Acid SCHEMBL2173045 0.87 ALDH1A1 (0.52) ALDH1A1L3MBTL1TSHRTDP1THRB
Trifluoroacetic Acid SCHEMBL2484766 0.84 ALDH1A1 (0.44) ALDH1A1L3MBTL1TSHRTHRBCA2
Trifluoroacetic Acid SCHEMBL474 0.84
Trifluoroacetic Acid SCHEMBL4598430 0.84
Trifluoroacetic Acid SCHEMBL7814389 0.84 ALDH1A1 (0.44) ALDH1A1L3MBTL1TSHRTHRBCA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117924066-A Trifluoroacetic acid purification method 四川熔增环保科技有限公司 2024-04-26 CN claimed
CN-117865911-A Preparation method of 3-methyl-1, 2, 4-thiadiazole-5-carbohydrazide 成都科圣原医药科技有限公司 2024-04-12 CN claimed
CN-110317212-B Synthesis of polycyclic carbamoylpyridone compounds 吉利德科学公司 2022-10-21 CN claimed
EP-3527573-B9 SYNTHESIS OF POLYCYCLIC-CARBAMOYLPYRIDONE COMPOUNDS GILEAD SCIENCES INC (US) 2022-07-06 EP claimed
CN-114394983-A Synthesis of polycyclic carbamoylpyridone compounds 吉利德科学公司 2022-04-26 CN claimed
US-10975096-B2 Synthesis of polycyclic-carbamoylpyridone compounds GILEAD SCIENCES, INC. (US) 2021-04-13 US claimed
EP-3783001-A1 SYNTHESIS OF POLYCYCLIC-CARBAMOYLPYRIDONE COMPOUNDS Gilead Sciences, Inc. (US) 2021-02-24 EP claimed
EP-3527573-B1 SYNTHESIS OF POLYCYCLIC-CARBAMOYLPYRIDONE COMPOUNDS GILEAD SCIENCES INC (US) 2020-08-12 EP claimed
US-20200223866-A1 SYNTHESIS OF POLYCYCLIC-CARBAMOYLPYRIDONE COMPOUNDS GILEAD SCIENCES, INC. 2020-07-16 US claimed
CN-110317212-A The synthesis of polycyclic carbamoylpyridone compound 吉利德科学公司 2019-10-11 CN claimed
WO-2015195656-A2 SYNTHESIS OF POLYCYCLIC-CARBAMOYLPYRIDONE COMPOUNDS GILEAD SCIENCES ,INC. (US) 2015-12-23 WO claimed
CN-104230782-A Synthetic method of silodosin KUNMING JIDA PHARMACEUTICAL CO LTD 2014-12-24 CN claimed
US-20130012736-A1 METHYLIDENE MALONATE PROCESS OPTMED, INC. (US) 2013-01-10 US claimed
US-20090124814-A1 Process for preparing telmisartan PERLMAN NURIT 2009-05-14 US claimed
EP-1699765-A1 PROCESS FOR PREPARING TELMISARTAN Teva Pharmaceutical Industries Ltd (IL) 2006-09-13 EP claimed
US-20060094883-A1 high yields, low cost process; easy solvent extraction; nontoxic, safe, environmentally friendly, low boiling point organic solvents; 1,7'-dimethyl-2'-propyl-1H,3'H-[2,5']bibenzoimidazolyl is reacted with 4'bromomethyl-biphenyl-2-carboxylic acid alkyl ester; industrial scale; hydrolysis TEVA PHARMACEUTICALS USA, INC. 2006-05-04 US claimed
WO-2006044648-A1 PROCESS FOR PREPARING TELMISARTAN TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2006-04-27 WO claimed
EP-0035881-B1 2,3,4,5,6,7-HEXAHYDRO-10-HYDROXY-2-METHYL-8-PHENYL-8H-FURO(3,2-G)-3-BENZAZEPINES, PROCESS FOR THEIR PREPARATION AND COMPOSITIONS CONTAINING THEM SMITHKLINE BECKMAN CORPORATION (US) 1985-07-17 EP claimed
EP-0035881-A1 2,3,4,5,6,7-Hexahydro-10-hydroxy-2-methyl-8-phenyl-8H-furo(3,2-g)-3-benzazepines, process for their preparation and compositions containing them SMITHKLINE BECKMAN CORPORATION (US) 1981-09-16 EP claimed
US-4255445-A DOPAMINERGIC ACTIVITY, RENAL VASODILATING ACTIVITY SMITHKLINE CORPORATION (US) 1981-03-10 US claimed

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

For each of this compound's patents that has machine-readable text (5 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-20200223866-A1 SYNTHESIS OF POLYCYCLIC-CARBAMOYLPYRIDONE COMPOUNDS CPS1, SDHA, DHPS ALDH1A1 883/4885L3MBTL1 4723/4885CA5A 283/4885
US-20130012736-A1 METHYLIDENE MALONATE PROCESS MPHOSPH6, ME1, MGAM ALDH1A1 1618/4885L3MBTL1 958/4885CA5A 4030/4885
US-20060094883-A1 high yields, low cost process; easy solvent extraction; nontoxic, safe, environmentally friendly, low boiling point organic solvents; 1,7'-dimethyl-2'-propyl-1H,3'H-[2,5']bibenzoimidazolyl is reacted with 4'bromomethyl-biphenyl-2-carboxylic acid alkyl ester; industrial scale; hydrolysis AGT, ACE, REN ALDH1A1 1639/4885L3MBTL1 3642/4885CA5A 3186/4885
US-20090124814-A1 Process for preparing telmisartan AGT, ACE, REN ALDH1A1 2133/4885L3MBTL1 4842/4885CA5A 3842/4885
US-10975096-B2 Synthesis of polycyclic-carbamoylpyridone compounds CPS1, SDHA, DHPS ALDH1A1 883/4885L3MBTL1 4723/4885CA5A 283/4885

“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.