Sulfuric Acid

Sulfuric Acid

SCHEMBL8501566

Nc1ccccc1CCO.O=C([O-])[O-].O=S(=O)(O)O.[K+].[K+]

nearest known ligand 0.36

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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
CA1 P00915 4/20 0.36
CA2 P00918 4/20 0.36
CA9 Q16790 3/20 0.36
CA12 O43570 2/20 0.36
CA4 P22748 2/20 0.36
CA6 P23280 2/20 0.36
CA5A P35218 2/20 0.36
CA7 P43166 2/20 0.36
CA14 Q9ULX7 2/20 0.36
CA5B Q9Y2D0 2/20 0.36
FDPS P14324 1/20 0.36
GAA P10253 3/20 0.34
KDM4E B2RXH2 3/20 0.34
MAPT P10636 2/20 0.34
ALDH1A1 P00352 2/20 0.34
LMNA P02545 1/20 0.34
CYP3A4 P08684 1/20 0.34
BLM P54132 1/20 0.34
GFER P55789 1/20 0.34
PMP22 Q01453 1/20 0.34

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 SCHEMBL8441339 0.91 FDPS (0.39) CA1CA2CA9CA12CA4
Sulfuric Acid SCHEMBL7093205 0.91 FDPS (0.41) CA1CA2CA9CA12CA4
SCHEMBL249418 0.82 TDP1 (0.44) FDPSKDM4EMAPTALDH1A1CYP3A4
Hydrochloric Acid SCHEMBL7205319 0.80 TDP1 (0.42) FDPSKDM4EMAPTALDH1A1CYP3A4
Sulfuric Acid SCHEMBL14830445 0.77 TTR (0.38) CA1CA2CA9CA12CA4
Acrylic Acid SCHEMBL27927427 0.75 ALDH1A1 (0.38) FDPSGAAKDM4EMAPTALDH1A1
Sulfuric Acid SCHEMBL9293766 0.74 GABRA1 (0.44) CA1CA2CA9CA12CA4
Sulfuric Acid SCHEMBL28641532 0.74 CA1 (0.39) CA1CA2CA9CA12CA4
SCHEMBL8767340 0.73 FDPS (0.41) CA1CA2CA9CA12CA4
SCHEMBL9177470 0.72 FDPS (0.38) CA1CA2CA9CA12CA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5998117-A METHINE DYE CAPABLE OF BEING DECOLORED BY REACTING WITH A COLOR DEVELOPING AGENT. KONICA CORPORATION (JP) 1999-12-07 US disclosed