Trifluoroacetic Acid

Trifluoroacetic Acid

SCHEMBL3149138

NCCN.O=C(O)C(F)(F)F

nearest known ligand 0.41

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADORA1ADORA2AADORA2BADORA3PDE3APDE3BPDE4APDE4BPDE4CPDE4D

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
HRH4 Q9H3N8 2/20 0.41
HRH3 Q9Y5N1 2/20 0.41
ODC1 P11926 2/20 0.41
CA12 O43570 2/20 0.41
CA1 P00915 2/20 0.41
CA2 P00918 2/20 0.41
CA9 Q16790 2/20 0.41
GLRA1 P23415 1/20 0.39
SLC6A9 P48067 1/20 0.39
OR51E2 Q9H255 1/20 0.39
LMNA P02545 2/20 0.38
BLM P54132 2/20 0.38
KDM4E B2RXH2 1/20 0.38
MAPT P10636 1/20 0.38
RAB9A P51151 1/20 0.38
PMP22 Q01453 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
HDAC6 Q9UBN7 2/20 0.36
GABRR3 A8MPY1 1/20 0.36
GABRP O00591 1/20 0.36

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 SCHEMBL10619788 1.00 HRH4 (0.41) HRH4HRH3ODC1CA12CA1
Trifluoroacetic Acid SCHEMBL11052838 0.97 HRH4 (0.40) HRH4HRH3ODC1CA12CA1
Trifluoroacetic Acid SCHEMBL6490887 0.88 HRH4 (0.50) HRH4HRH3ODC1CA12CA1
Trifluoroacetic Acid SCHEMBL10619767 0.88 ODC1 (0.48) HRH4HRH3ODC1CA12CA1
Trifluoroacetic Acid SCHEMBL1833664 0.88 TSHR (0.47) HRH4HRH3ODC1CA12CA1
Trifluoroacetic Acid SCHEMBL3149196 0.88 ODC1 (0.48) HRH4HRH3ODC1CA12CA1
Trifluoroacetic Acid SCHEMBL29019099 0.87 GABRR1 (0.41) HRH4HRH3ODC1CA12CA1
Trifluoroacetic Acid SCHEMBL28235039 0.86 ALDH1A1 (0.38) ODC1CA2SMN1; SMN2THRBTSHR
Diaminooctane SCHEMBL31657050 0.85 MEN1 (0.52) HRH4HRH3ODC1CA12CA1
Trifluoroacetic Acid SCHEMBL31657036 0.85 MEN1 (0.52) HRH4HRH3ODC1CA12CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115915795-A Perovskite solar cell containing double-layer trifluoroacetate modification layer and preparation method thereof 河北工业大学 2023-04-04 CN claimed
CN-1606439-A Cis-imidazolines HOFFMANN LA ROCHE (CH) 2005-04-13 CN claimed
CN-115915795-A Perovskite solar cell containing double-layer trifluoroacetate modification layer and preparation method thereof 河北工业大学 2023-04-04 CN disclosed
CN-115915795-A Perovskite solar cell containing double-layer trifluoroacetate modification layer and preparation method thereof 河北工业大学 2023-04-04 CN disclosed
CN-109265400-B Arginine methyltransferase inhibitors and uses thereof EPIZYME股份有限公司 2022-10-04 CN disclosed
CN-111093645-A Selective inhibitors of clinically important mutants of EGFR tyrosine kinase CS制药技术有限公司 2020-05-01 CN disclosed
EP-2763990-B1 PYRROLOPYRAZINE KINASE INHIBITORS HOFFMANN LA ROCHE (CH) 2017-02-22 EP disclosed
EP-2763990-A1 PYRROLOPYRAZINE KINASE INHIBITORS F.HOFFMANN-LA ROCHE AG (CH) 2014-08-13 EP disclosed
US-8658646-B2 Pyrrolopyrazine kinase inhibitors HOFFMANN-LAROCHE INC. (US) 2014-02-25 US disclosed
WO-2013030138-A1 PYRROLOPYRAZINE KINASE INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2013-03-07 WO disclosed
US-20130059834-A1 PYRROLOPYRAZINE KINASE INHIBITORS HOFFMANN-LA ROCHE INC. 2013-03-07 US disclosed
US-20090093633-A1 Organic Compounds NOVARTIS AG 2009-04-09 US disclosed
EP-2012759-A1 PURINE DERIVATIVES AS A2A RECEPTOR AGONISTS Novartis AG (CH) 2009-01-14 EP disclosed
EP-1841768-B1 PURINE DERIVATIVES ACTING AS A2A RECEPTOR AGONISTS NOVARTIS AG (CH) 2008-11-12 EP disclosed
US-20080207648-A1 Organic Compounds NOVARTIS AG (CH) 2008-08-28 US disclosed
WO-2007121923-A1 PURINE DERIVATIVES AS A2A RECEPTOR AGONISTS NOVARTIS AG (CH) 2007-11-01 WO disclosed
EP-1841768-A1 PURINE DERIVATIVES ACTING AS A2A RECEPTOR AGONISTS Novartis AG (CH) 2007-10-10 EP disclosed
WO-2006074925-A1 PURINE DERIVATIVES ACTING AS A2A RECEPTOR AGONISTS NOVARTIS AG (CH) 2006-07-20 WO disclosed
EP-1458378-B1 AMINO ACID DERIVATIVES USEFUL FOR THE TREATMENT OF ALZHEIMER'S DISEASE ELAN PHARM INC (US) 2006-05-24 EP disclosed
CN-1606439-A Cis-imidazolines HOFFMANN LA ROCHE (CH) 2005-04-13 CN 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 (3 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-20090093633-A1 Organic Compounds ADORA2A, ADORA3, ADORA1 HRH4 496/4885HRH3 628/4885ODC1 898/4885
US-20130059834-A1 PYRROLOPYRAZINE KINASE INHIBITORS SYK, ZAP70, JAK1 HRH4 1867/4885HRH3 2710/4885ODC1 1991/4885
US-20080207648-A1 Organic Compounds ADORA2A, ADORA1, ADORA3 HRH4 181/4885HRH3 318/4885ODC1 422/4885

“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.