Trifluoromethanesulfonic Acid

Trifluoromethanesulfonic Acid

SCHEMBL4920095

C=CCn1cc[n+](C)c1.O=S(=O)([O-])C(F)(F)F

nearest known ligand 0.37

Full drug profile on Sugi Atlas →

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
FDPS P14324 2/20 0.37
SMN1; SMN2 Q16637 2/20 0.33
MEN1 O00255 1/20 0.33
APAF1 O14727 1/20 0.33
NPC1 O15118 1/20 0.33
PLA2G1B P04054 1/20 0.33
HSP90AA1 P07900 1/20 0.33
MAPT P10636 1/20 0.33
MAPK1 P28482 1/20 0.33
HTT P42858 1/20 0.33
RAB9A P51151 1/20 0.33
KMT2A Q03164 1/20 0.33
NPSR1 Q6W5P4 1/20 0.33
ATG4B Q9Y4P1 1/20 0.33
KCNH2 Q12809 6/20 0.31
ACHE P22303 1/20 0.31
LMNA P02545 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.

Compoundsimilaritytop predictedshared targets
Trifluoromethanesulfonic Acid SCHEMBL16668993 0.95 FDPS (0.36) FDPSSMN1; SMN2MEN1APAF1NPC1
Sulfuric Acid SCHEMBL30712585 0.89 FDPS (0.39) FDPSSMN1; SMN2MEN1APAF1NPC1
SCHEMBL4281206 0.88 FDPS (0.38) FDPSSMN1; SMN2MEN1APAF1NPC1
Sulfuric Acid SCHEMBL1101232 0.86 FDPS (0.40) FDPSSMN1; SMN2MEN1APAF1NPC1
SCHEMBL2691328 0.86 FDPS (0.33) FDPSSMN1; SMN2MEN1APAF1NPC1
Trifluoromethanesulfonic Acid SCHEMBL2028441 0.84 FDPS (0.36) FDPSSMN1; SMN2MEN1APAF1NPC1
SCHEMBL9934092 0.84 FDPS (0.38) FDPSSMN1; SMN2MEN1APAF1NPC1
SCHEMBL14635383 0.84 FDPS (0.35) FDPSSMN1; SMN2MEN1APAF1NPC1
Sulfuric Acid SCHEMBL28517102 0.83 FDPS (0.39) FDPSSMN1; SMN2MEN1APAF1NPC1
Trifluoromethanesulfonic Acid SCHEMBL16108388 0.82

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119833706-A Three-dimensional solid lithium battery and preparation method thereof 东莞市威力源电子科技有限公司 2025-04-15 CN claimed
US-20080015362-A1 Process for the preparation of optically active (S)-(+)-N,N-dimethyl-3-(1-naphthalenyloxy)-3-(2-thienyl)propanamine TEVA PHARMACEUTICALS USA, INC. 2008-01-17 US claimed
US-20070238883-A1 Process for the preparation of(s)-(+)-N,N-dimethyl-3-(1-Naphthalenyloxy)-3-(2-Thienyl)propanamine, A duloxetine intermediate TEVA PHARMACEUTICALS USA, INC. 2007-10-11 US claimed
CN-119833706-A Three-dimensional solid lithium battery and preparation method thereof 东莞市威力源电子科技有限公司 2025-04-15 CN disclosed
CN-116685468-A Surface protective film 日东电工株式会社 2023-09-01 CN disclosed
EP-3774762-B1 PROCESS FOR PRODUCING A CYCLIC ACETAL IN A HETEROGENEOUS REACTION SYSTEM CELANESE SALES GERMANY GMBH (DE) 2023-08-30 EP disclosed
CN-116670242-A Surface protective film 日东电工株式会社 2023-08-29 CN disclosed
CN-116635228-A Surface protective film 日东电工株式会社 2023-08-22 CN disclosed
CN-116438273-A Film with adhesive layer 日东电工株式会社 2023-07-14 CN disclosed
EP-3774762-A1 PROCESS FOR PRODUCING A CYCLIC ACETAL IN A HETEROGENEOUS REACTION SYSTEM Celanese Sales Germany GmbH (DE) 2021-02-17 EP disclosed
CN-111971276-A Method for producing cyclic acetals in heterogeneous reaction systems 塞拉尼斯销售德国有限公司 2020-11-20 CN disclosed
US-9499512-B2 Process for producing a cyclic acetal in a heterogeneous reaction system TICONA GMBH (DE) 2016-11-22 US disclosed
US-20140350216-A1 Process for Producing A Cyclic Acetal In A Heterogeneous Reaction System NUTRINOVA NUTRITION SPECIALTIES & FOOD INGREDIENTS GMBH (DE) 2014-11-27 US disclosed
EP-2782908-A1 PROCESS FOR PRODUCING A CYCLIC ACETAL IN A HETEROGENEOUS REACTION SYSTEM Ticona GmbH (DE) 2014-10-01 EP disclosed
US-20140182484-A1 Process For Producing Polyoxymethylene Polymers With Long-Chain Alkyl End Groups, and Polymers Made Therefrom TICONA GMBH (DE) 2014-07-03 US disclosed
US-20140182485-A1 Polyoxymethylene Polymer With Long Chain Alkylene Glycol End Groups TICONA GMBH (DE) 2014-07-03 US disclosed
WO-2013076290-A1 PROCESS FOR PRODUCING A CYCLIC ACETAL IN A HETEROGENEOUS REACTION SYSTEM TICONA GMBH (DE) 2013-05-30 WO disclosed
US-20120126931-A1 ELECTROLYTE COMPOSITION SERICOL LIMITED (GB) 2012-05-24 US disclosed
US-20080015362-A1 Process for the preparation of optically active (S)-(+)-N,N-dimethyl-3-(1-naphthalenyloxy)-3-(2-thienyl)propanamine TEVA PHARMACEUTICALS USA, INC. 2008-01-17 US disclosed
US-20070238883-A1 Process for the preparation of(s)-(+)-N,N-dimethyl-3-(1-Naphthalenyloxy)-3-(2-Thienyl)propanamine, A duloxetine intermediate TEVA PHARMACEUTICALS USA, INC. 2007-10-11 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 (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-20080015362-A1 Process for the preparation of optically active (S)-(+)-N,N-dimethyl-3-(1-naphthalenyloxy)-3-(2-thienyl)propanamine HTR3A, PNMT, TPH1 FDPS 1003/4885SMN1; SMN2 302/4885MEN1 3527/4885
US-20140350216-A1 Process for Producing A Cyclic Acetal In A Heterogeneous Reaction System ATIC, DCXR, ALDOA FDPS 137/4885SMN1; SMN2 3068/4885MEN1 4213/4885
US-20070238883-A1 Process for the preparation of(s)-(+)-N,N-dimethyl-3-(1-Naphthalenyloxy)-3-(2-Thienyl)propanamine, A duloxetine intermediate DNTT, NES, PNMT FDPS 1593/4885SMN1; SMN2 198/4885MEN1 3014/4885

“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.