Trifluoromethanesulfonic Acid

Trifluoromethanesulfonic Acid

SCHEMBL28047635

C[N+](C)(C)CCO.O=S(=O)(O)C(F)(F)F

nearest known ligand 0.55

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Known targets — ChEMBL curated mechanism

ADORA1ADORA2AADORA2BADORA3GNRHRMPLPDE3APDE3BPDE4APDE4BPDE4CPDE4DPPARASLC5A2

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

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.52
LMNA P02545 1/20 0.52
KMT2A Q03164 1/20 0.52
CYP3A4 P08684 1/20 0.52
SLC5A7 Q9GZV3 1/20 0.52
BBOX1 O75936 1/20 0.32
SLC6A4 P31645 1/20 0.32
L3MBTL1 Q9Y468 2/20 0.31
ALDH1A1 P00352 1/20 0.31
APAF1 O14727 1/20 0.30
POLB P06746 1/20 0.30
GRK2 P25098 1/20 0.30
DNMT1 P26358 1/20 0.30
PTPN7 P35236 1/20 0.30
RECQL P46063 1/20 0.30
BLM P54132 1/20 0.30
PPP1CA P62136 1/20 0.30
CTDSP1 Q9GZU7 1/20 0.30
PTPN22 Q9Y2R2 1/20 0.30

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
Trifluoromethanesulfonic Acid SCHEMBL29160398 0.98 CYP3A4 (0.56) MEN1LMNAKMT2ACYP3A4SLC5A7
Choline SCHEMBL28499286 0.88 CYP3A4 (0.50) MEN1LMNAKMT2ACYP3A4SLC5A7
Trifluoromethanesulfonic Acid SCHEMBL3008777 0.86 L3MBTL1 (0.40) MEN1LMNAKMT2ACYP3A4SLC5A7
Trifluoromethanesulfonamide SCHEMBL28047636 0.84 LMNA (0.50) MEN1LMNAKMT2ACYP3A4SLC5A7
Trifluoromethanesulfonic Acid SCHEMBL3785097 0.84 MEN1 (0.50) MEN1LMNAKMT2ACYP3A4SLC5A7
Trifluoromethanesulfonamide SCHEMBL28047774 0.84 LMNA (0.50) MEN1LMNAKMT2ACYP3A4SLC5A7
Choline SCHEMBL393397 0.83 MEN1 (0.67) MEN1LMNAKMT2ACYP3A4SLC5A7
Choline SCHEMBL27857086 0.82 MEN1 (0.43) MEN1LMNAKMT2ACYP3A4SLC5A7
Choline SCHEMBL28501392 0.82 CYP3A4 (0.48) MEN1LMNAKMT2ACYP3A4SLC5A7
Choline SCHEMBL933567 0.81 MEN1 (0.46) MEN1LMNAKMT2ACYP3A4SLC5A7

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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105503540-A Method for preparation of benzene ring phenol compound from alkali lignin DALIAN INST CHEMICAL PHYSICS CAS 2016-04-20 CN claimed
CN-105315164-A Environment-friendly choline ionic liquid and preparation method therefor DALIAN CHEMICAL PHYSICS INST 2016-02-10 CN claimed
CN-114390909-B Manufacturing technology of skin compatible electrode 荷兰应用自然科学研究组织TNO 2024-09-20 CN disclosed
CN-117941116-A Ionic binders for solid state electrodes 迪金大学 2024-04-26 CN disclosed
CN-115989294-A Dry stimulating electrode 汉高股份有限及两合公司 2023-04-18 CN disclosed
CN-105503540-A Method for preparation of benzene ring phenol compound from alkali lignin DALIAN INST CHEMICAL PHYSICS CAS 2016-04-20 CN disclosed
CN-105315164-A Environment-friendly choline ionic liquid and preparation method therefor DALIAN CHEMICAL PHYSICS INST 2016-02-10 CN disclosed
CN-105315164-A Environment-friendly choline ionic liquid and preparation method therefor DALIAN CHEMICAL PHYSICS INST 2016-02-10 CN disclosed