Trifluoromethanesulfonic Acid

Trifluoromethanesulfonic Acid

SCHEMBL6923670

O=S(=O)(O)C(F)(F)F.[Se]c1ccccc1

nearest known ligand 0.50

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 2/20 0.50
CA2 P00918 2/20 0.50
CA9 Q16790 2/20 0.50
CA7 P43166 1/20 0.50
PTPN1 P18031 3/20 0.42
TSHR P16473 2/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
CA5A P35218 1/20 0.39
CES1 P23141 2/20 0.37
ALDH1A1 P00352 3/20 0.36
L3MBTL1 Q9Y468 1/20 0.36
GPR3 P46089 1/20 0.34
HSD11B1 P28845 1/20 0.34
SRC P12931 1/20 0.33
PSIP1 O75475 1/20 0.33
HTR6 P50406 1/20 0.33
POLB P06746 1/20 0.32
CYP2D6 P10635 1/20 0.32
FAAH O00519 1/20 0.32
PRSS1 P07477 1/20 0.32

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
Biphenyl SCHEMBL1050411 0.81 PTPN1 (0.58) CA1CA2CA9PTPN1TSHR
Trifluoromethanesulfonic Acid SCHEMBL789189 0.80 ALDH1A1 (0.50) CA1CA2CA9CA7PTPN1
Trifluoromethanesulfonic Acid SCHEMBL30552135 0.80 ALDH1A1 (0.50) CA1CA2CA9CA7PTPN1
Trifluoromethanesulfonic Acid SCHEMBL29657724 0.79 CA1 (0.52) CA1CA2CA9PTPN1TSHR
Biphenyl SCHEMBL304392 0.79 PTPN1 (0.56) CA1CA2CA9PTPN1TSHR
Biphenyl SCHEMBL5410059 0.79 PTPN1 (0.56) CA1CA2CA9PTPN1TSHR
Trifluoromethanesulfonic Acid SCHEMBL3345470 0.79 CA1 (0.52) CA1CA2CA9PTPN1TSHR
Biphenyl SCHEMBL2192409 0.79 PTPN1 (0.56) CA1CA2CA9PTPN1TSHR
Trifluoromethanesulfonic Acid SCHEMBL9470710 0.79 CA1 (0.52) CA1CA2CA9PTPN1TSHR
Naphthalene SCHEMBL7160995 0.78 ALOX12 (0.42) CA1CA2CA9PTPN1TSHR

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-103476782-A N-substituted mannosamine derivatives, process for their preparation and their use GLYCOM AS 2013-12-25 CN disclosed
EP-0686160-A4 SOLUTION AND SOLID-PHASE FORMATION OF GLYCOSIDIC LINKAGES UNIV PRINCETON (US) 2003-03-12 EP disclosed
US-6194393-B1 A GLYCOSIDE CONTAINING AN ANOMERIC SULFOXIDE AND NUCLEOPHILIC FUNCTIONAL GROUPS AND HAVING POTENTIAL GLYCOSYL ACCEPTING/DONATING CHARACTERISTICS AND AN ACTIVATING AGENT; RAPID CONSTRUCTION OLIGOSACCHARIDES; GLYCOSYLATION; LIBRARY THE TRUSTEES OF PRINCETON UNIVERSITY 2001-02-27 US disclosed
US-5861492-A LIBRARIES OF SULFOXIDE-SUBSTITUTED GLYCOSIDES WHICH CAN BIND TO OTHER GLYCOSIDES, STEROIDS, AMINO ACIDS, PEPTIDES, LIPIDS OR POLYCYCLIC AROMATIC COMPOUNDS; FOR RAPID, EFFICIENT, SELECTIVE, MULTIPLE GLYCOSYLATION REACTIONS IN ONE STEP THE TRUSTEES OF PRINCETON UNIVERSITY (US) 1999-01-19 US disclosed
US-5792839-A REACTING GLCOSYL DONOR HAVING ANOMERIC SULFOXIDE GROUP AND GLYCOSYL ACCEPTOR AT LOW TEMPERATURE TRUSTEES OF PRINCETON UNIVERSITY (US) 1998-08-11 US disclosed
US-5700916-A INTERMEDIATES FOR FORMING OLIGOSACCHARIDES, INCLUDING 4-HYDROXYTHIOPHENYL-/2-AZIDO-2-DEOXYGLUCO/PYRANOSIDE TRUSTEES OF PRINCETON UNIVERSITY (US) 1997-12-23 US disclosed
EP-0686160-A1 SOLUTION AND SOLID-PHASE FORMATION OF GLYCOSIDIC LINKAGES THE TRUSTEES OF PRINCETON UNIVERSITY (US) 1995-12-13 EP disclosed
WO-1994019360-A1 SOLUTION AND SOLID-PHASE FORMATION OF GLYCOSIDIC LINKAGES THE TRUSTEES OF PRINCETON UNIVERSITY (US) 1994-09-01 WO disclosed