Sulfuric Acid

Sulfuric Acid

SCHEMBL8720422

O=S(=O)(O)F.O=S(=O)(O)O

nearest known ligand 0.89

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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 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.89
TDP1 Q9NUW8 1/20 0.89
CA5A P35218 2/20 0.67
CA5B Q9Y2D0 2/20 0.67
CA2 P00918 2/20 0.46
CA1 P00915 1/20 0.42
NT5E P21589 1/20 0.42
CA4 P22748 1/20 0.42
CA6 P23280 1/20 0.42
CA7 P43166 1/20 0.42
CA9 Q16790 1/20 0.42
BLM P54132 2/20 0.40
KDM4E B2RXH2 2/20 0.40
ALDH1A1 P00352 2/20 0.39
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39
CYP2D6 P10635 1/20 0.32
CYP2C19 P33261 1/20 0.32
NPSR1 Q6W5P4 1/20 0.32
L3MBTL1 Q9Y468 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
SCHEMBL29818845 0.94 TSHR (1.00) TSHRTDP1CA5ACA5BCA2
SCHEMBL1938 0.94
SCHEMBL8378123 0.89
SCHEMBL8377677 0.89
SCHEMBL8376424 0.89
Lithium SCHEMBL929003 0.89 TSHR (0.89) TSHRTDP1CA5ACA5BCA2
SCHEMBL6223954 0.89
Methane SCHEMBL9362880 0.89
SCHEMBL7249115 0.89
SCHEMBL3422882 0.89 TSHR (0.89) TSHRTDP1CA5ACA5BCA2

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
US-4033899-A Alkylation fluosulfonic-sulfuric acid catalyst recovery process with silica-alumina removal of fluoride compounds TEXACO INC. (US) 1977-07-05 US claimed
US-11324903-B2 To the manufacture and remanufacture of volatile anaesthetic agents using supercritical fluids SAGETECH MEDICAL EQUIPMENT LIMITED (GB) 2022-05-10 US disclosed
US-20190275275-A1 IMPROVEMENTS TO THE MANUFACTURE AND REMANUFACTURE OF VOLATILE ANAESTHETIC AGENTS USING SUPERCRITICAL FLUIDS SAGETECH MEDICAL EQUIPMENT LIMITED (GB) 2019-09-12 US disclosed
EP-3419739-A1 IMPROVEMENTS TO THE MANUFACTURE AND REMANUFACTURE OF VOLATILE ANAESTHETIC AGENTS USING SUPERCRITICAL FLUIDS Sagetech Medical Equipment Limited (GB) 2019-01-02 EP disclosed
WO-2017144879-A1 IMPROVEMENTS TO THE MANUFACTURE AND REMANUFACTURE OF VOLATILE ANAESTHETIC AGENTS USING SUPERCRITICAL FLUIDS SAGETECH MEDICAL EQUIPMENT LIMITED (GB) 2017-08-31 WO disclosed
US-5744116-A Reaction of uranium fluorides with mineral acids to recover hydrogen fluoride CAMECO CORPORATION (CA) 1998-04-28 US disclosed
WO-1996017802-A1 CONVERSION OF URANIUM FLUORIDES TO OXIDES AND ANHYDROUS HYDROGEN FLUORIDE BY REACTION WITH SULPHURIC ACID CAMECO CORPORATION (CA) 1996-06-13 WO disclosed
US-4033899-A Alkylation fluosulfonic-sulfuric acid catalyst recovery process with silica-alumina removal of fluoride compounds TEXACO INC. (US) 1977-07-05 US disclosed