Sulfuric Acid

Sulfuric Acid

SCHEMBL5200253

FC(F)F.O=S(=O)(O)O.[Ag]

nearest known ligand 0.55

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

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

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CA5A P35218 2/20 0.55
CA5B Q9Y2D0 2/20 0.55
TSHR P16473 3/20 0.46
TDP1 Q9NUW8 1/20 0.46
CA2 P00918 2/20 0.36
CA1 P00915 1/20 0.36
NT5E P21589 1/20 0.36
CA4 P22748 1/20 0.36
CA6 P23280 1/20 0.36
CA7 P43166 1/20 0.36
CA9 Q16790 1/20 0.36
BLM P54132 1/20 0.35
KDM4E B2RXH2 1/20 0.35
MEN1 O00255 1/20 0.33
ALDH1A1 P00352 1/20 0.33
KMT2A Q03164 1/20 0.33

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
Sulfuric Acid SCHEMBL152452 0.95
Sulfuric Acid SCHEMBL28756197 0.91 CA5A (0.55) CA5ACA5BTSHRTDP1CA2
Sulfuric Acid SCHEMBL4795542 0.91 CA5A (0.55) CA5ACA5BTSHRTDP1CA2
Sulfuric Acid SCHEMBL9568493 0.91 CA5A (0.55) CA5ACA5BTSHRTDP1CA2
Sulfuric Acid SCHEMBL20641565 0.91 CA5A (0.55) CA5ACA5BTSHRTDP1CA2
Sulfuric Acid SCHEMBL408154 0.91 CA5A (0.55) CA5ACA5BTSHRTDP1CA2
Sulfuric Acid SCHEMBL10878652 0.87 TSHR (0.67) CA5ACA5BTSHRTDP1CA2
Sulfuric Acid SCHEMBL5042267 0.80 CA5A (0.86) CA5ACA5BTSHRTDP1CA2
Sulfuric Acid SCHEMBL2110347 0.80
Sulfuric Acid SCHEMBL28294145 0.80 CA5A (0.86) CA5ACA5BTSHRTDP1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2015056993-A1 COMBINATION OF A HOST COMPOUND AND A DOPANT COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME ROHM AND HAAS ELECTRONIC MATERIALS KOREA LTD. (KR) 2015-04-23 WO disclosed
EP-1247814-B1 TRANSITION METAL COMPOUNDS, POLYMERIZATION CATALYSTS FOR OLEFINS, OLEFIN POLYMERS AND PROCESS FOR THEIR PRODUCTION IDEMITSU KOSAN CO (JP) 2007-08-22 EP disclosed
US-6770772-B2 DOUBLE CROSS-LINKED METALLOCENE COMPLEX; HIGH MOLECULAR WEIGHT, STEREOSPECIFIC; NARROW MOLECULAR WEIGHT DISTRIBUTION IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2004-08-03 US disclosed
EP-1115729-B1 PHOSPHONIC ACID DERIVATIVES AS INHIBITORS OF PTP-1B MERCK FROSST CANADA INC (CA) 2003-02-19 EP disclosed
US-20030017940-A1 Transition metal compound, polymerization catalysts for olefin , olefin polymers and process for their production IDEMITSU KOSAN CO. LTD. (JP) 2003-01-23 US disclosed
EP-1247814-A1 TRANSITION METAL COMPOUNDS, POLYMERIZATION CATALYSTS FOR OLEFINS, OLEFIN POLYMERS AND PROCESS FOR THEIR PRODUCTION IDEMITSU PETROCHEMICAL CO., LTD. (JP) 2002-10-09 EP disclosed
EP-1115729-A1 PHOSPHONIC ACID DERIVATIVES AS INHIBITORS OF PTP-1B Merck Frosst Canada & Co. (CA) 2001-07-18 EP disclosed
US-6174874-B1 ANTIDIABETIC,-CARCINOGENIC AGENTS; IMPROVING GLUCOSE TOLERANCE/INSULIN-SENSITIVITY; PREVENTING/TREATING OBESITY AND NEURODEGENERATIVE DISEASES; E.G. 1,3-BIS-((PHOSPHONODI-FLUOROMETHYL)PHENYL)-2-DICARBOXYPROPANE MERCK FROSST CANADA & CO. (CA) 2001-01-16 US disclosed
WO-2000017211-A1 PHOSPHONIC ACIDS DERIVATIVES AS INHIBITORS OF PTP-1B MERCK FROSST CANADA & CO. (CA) 2000-03-30 WO disclosed
EP-0776328-B1 8-FLUORO-ANTHRACYCLINES, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM MENARINI FARMA IND (IT) 1998-11-04 EP disclosed
US-5814608-A S-fluoro-anthracyclines, processes for their preparation and pharmaceutical compositions containing them BRISTOL-MYERS SQUIBB, S.P.A. (IT) 1998-09-29 US disclosed
EP-0776328-A1 8-FLUORO-ANTHRACYCLINES, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM A. MENARINI INDUSTRIE FARMACEUTICHE RIUNITE S.R.L. (IT) 1997-06-04 EP disclosed
WO-1996004292-A1 8-FLUORO-ANTHRACYCLINES, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM A. MENARINI INDUSTRIE FARMACEUTICHE RIUNITE S.R.L. (IT) 1996-02-15 WO disclosed