Trifluoromethanesulfonamide

Trifluoromethanesulfonamide

SCHEMBL4288876

NS(=O)(=O)C(F)(F)F.O=S(=O)(Nc1ccccc1)C(F)(F)F

nearest known ligand 0.62

Full drug profile on Sugi Atlas →

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CA2 P00918 11/20 0.62
CA1 P00915 7/20 0.56
PTPN1 P18031 1/20 0.55
PTPN11 Q06124 1/20 0.53
MAPK1 P28482 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
PTGS1 P23219 1/20 0.49
PTGS2 P35354 1/20 0.49
CA5A P35218 1/20 0.47
CA9 Q16790 1/20 0.47
KEAP1 Q14145 2/20 0.45
IL1RN P18510 1/20 0.44
ERAP1 Q9NZ08 1/20 0.44
KDM1A O60341 1/20 0.43

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
SCHEMBL216185 0.92 PTPN1 (0.62) CA2CA1PTPN1PTPN11MAPK1
SCHEMBL28665290 0.90 PTPN1 (0.60) CA2CA1PTPN1PTPN11MAPK1
SCHEMBL1976973 0.90 PTPN1 (0.60) CA2CA1PTPN1PTPN11MAPK1
Diphenylamine SCHEMBL1060675 0.82 HSD17B10 (0.52) CA2CA1MAPK1PTGS1PTGS2
SCHEMBL19042259 0.80 CA2 (0.49) CA2CA1PTPN1PTPN11MAPK1
SCHEMBL17266478 0.79 PTPN1 (0.49) CA2CA1PTPN1PTPN11MAPK1
Trifluoromethanesulfonamide SCHEMBL4418171 0.79 CA2 (0.49) CA2CA1PTGS1PTGS2CA5A
SCHEMBL18048059 0.78 PTPN1 (0.51) CA2CA1PTPN1PTPN11MAPK1
SCHEMBL6001500 0.77 PTPN1 (0.86) CA2PTPN1PTPN11MAPK1SMN1; SMN2
SCHEMBL28027003 0.77 PTPN1 (0.54) CA2CA1PTPN1PTPN11MAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0919541-B1 Naphthalene compounds, process for their preparation and their pharmaceutical compositions SERVIER LAB (FR) 2005-08-10 EP claimed
EP-1038863-B1 Substituted dimeric compounds, process for their preparation and pharmaceutical compositions thereof SERVIER LAB (FR) 2003-06-04 EP claimed
EP-1057826-B1 Substituted dimeric carboxamide derivatives, method for preparing them, and pharmaceutical compositions containing them SERVIER LAB (FR) 2003-04-16 EP claimed
EP-0926145-A1 Napthalene compounds, method for their preparation and pharmaceutical compositions containing them ADIR ET COMPAGNIE (FR) 1999-06-30 EP claimed
CN-109476664-A New compound as autotaxin inhibitors and the pharmaceutical composition comprising it 乐高化学生物科学股份有限公司 2019-03-15 CN disclosed
CN-109053723-A Sulfamide derivative and its medicinal usage EA制药株式会社 2018-12-21 CN disclosed
WO-2009152102-A2 PRO-FLUORESCENT PROBES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2009-12-17 WO disclosed
EP-2125755-A2 QUINAZOLINES FOR PDK1 INHIBITION Novartis Ag (CH) 2009-12-02 EP disclosed
WO-2008079988-A2 QUINAZOLINES FOR PDK1 INHIBITION NOVARTIS AG (CH) 2008-07-03 WO disclosed
EP-0919541-B1 Naphthalene compounds, process for their preparation and their pharmaceutical compositions SERVIER LAB (FR) 2005-08-10 EP disclosed
US-6635650-B2 Such as N-(2-(7-(2-((8-(2-(acetyl-amino)ethyl)-2-naphthyl) oxy)ethoxy)-1-napthyl)ethyl)acetamide for treating or preventing melatoninergic disorders LES LABORATOIRES SERVIER (FR) 2003-10-21 US disclosed
US-20020035114-A1 Substituted dimeric compounds LESIEUR DANIEL (FR) 2002-03-21 US disclosed
US-6319930-B1 CONTAINING FUSED AROMATIC CARBO- OR HETEROCYCLIC RINGS AND AMIDE, THIOAMIDE, UREA OR THIOUREA GROUPS; USEFUL IN TREATING OR IN PREVENTING MELATONINERGIC DISORDERS. ADIR ET COMPAGNIE (FR) 2001-11-20 US disclosed
US-6310074-B1 TREATING MELATONINERGIC DISORDERS ADIR ET COMPAGNIE (FR) 2001-10-30 US disclosed
US-6147110-A MELATONINERGIC AGENTS; SLEEP, EATING, CENTRAL NERVOUS SYSTEM, AND CARDIOVASCULAR DISORDERS ADIR ET COMPAGNIE (FR) 2000-11-14 US disclosed
US-6143789-A ENANTIOMORPHS ADIR ET COMPAGNIE (FR) 2000-11-07 US disclosed
EP-0926145-A1 Napthalene compounds, method for their preparation and pharmaceutical compositions containing them ADIR ET COMPAGNIE (FR) 1999-06-30 EP disclosed
EP-0919541-A1 Naphthalene compounds, process for their preparation and their pharmaceutical compositions ADIR ET COMPAGNIE (FR) 1999-06-02 EP 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-20020035114-A1 Substituted dimeric compounds NR0B2, NR0B1, NR2C2 CA2 3267/4885CA1 3197/4885PTPN1 1525/4885

“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.