Sulfuric Acid

Sulfuric Acid

SCHEMBL4283485

Cc1cc(C)ncn1.O=S(=O)(O)O

nearest known ligand 0.34

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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
ALDH1A1 P00352 2/20 0.33
UHRF1 Q96T88 2/20 0.33
TDP1 Q9NUW8 2/20 0.33
ALOX15 P16050 1/20 0.33
MAPK1 P28482 1/20 0.33
HSD17B10 Q99714 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
SORT1 Q99523 1/20 0.33
KDM4E B2RXH2 1/20 0.32
GAA P10253 1/20 0.32
CA5A P35218 1/20 0.32
CA5B Q9Y2D0 1/20 0.32
LARS1 Q9P2J5 1/20 0.31
HTT P42858 3/20 0.31
NPC1 O15118 1/20 0.31
MITF O75030 1/20 0.31
LMNA P02545 1/20 0.31
MAPT P10636 1/20 0.31
RAB9A P51151 1/20 0.31
KMT2A Q03164 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
SCHEMBL161508 0.83
Formic Acid SCHEMBL27906957 0.79 ALDH1A1 (0.39) ALDH1A1UHRF1TDP1ALOX15MAPK1
SCHEMBL27257701 0.73 MAPT (0.32) ALDH1A1UHRF1TDP1KDM4EGAA
Sulfuric Acid SCHEMBL27717455 0.72 HTT (0.39) ALDH1A1TDP1ALOX15MAPK1KDM4E
Sulfuric Acid SCHEMBL28042580 0.70 KDM4E (0.33) ALDH1A1ALOX15HSD17B10L3MBTL1KDM4E
SCHEMBL26664408 0.70 ALDH1A1 (0.33) ALDH1A1UHRF1TDP1ALOX15MAPK1
Sulfuric Acid SCHEMBL4275195 0.69 CA5A (0.38) ALDH1A1TDP1ALOX15HSD17B10L3MBTL1
SCHEMBL882667 0.69 ALDH1A1 (0.39) ALDH1A1TDP1ALOX15MAPK1HSD17B10
Sulfuric Acid SCHEMBL6156212 0.68 NOS3 (0.48) ALDH1A1MAPK1HSD17B10KDM4EGAA
Sulfuric Acid SCHEMBL6214534 0.67 ALDH1A1 (0.50) ALDH1A1TDP1ALOX15MAPK1HSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7615644-B2 catalytic producing methanol from methane gas, by bubbling methane through the oxidation catalyst liquid mixture containing an imidazolium ionic liquid catalyst and a dissolved platinum compound as PtCl2, PtCl4, PtO2; cost efficiency, energy efficiency, low pollution, environmentally friendly CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2009-11-10 US disclosed
US-20060069169-A1 Use of ionic liquids as coordination ligands for organometallic catalysts CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2006-03-30 US disclosed
WO-2006033990-A2 USE OF IONIC LIQUIDS AS COORDINATION LIGANDS FOR ORGANOMETALLIC CATALYSTS CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2006-03-30 WO disclosed