Sulfuric Acid

Sulfuric Acid

SCHEMBL8501569

O=C([O-])[O-].O=S(=O)(O)O.O=S(=O)(O)O.OCCNc1ccccc1.OCCNc1ccccc1.[K+].[K+]

nearest known ligand 0.44

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 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 5/20 0.44
CA2 P00918 5/20 0.44
CA9 Q16790 4/20 0.44
ALDH1A1 P00352 2/20 0.44
MAPT P10636 2/20 0.44
RECQL P46063 1/20 0.44
MCL1 Q07820 1/20 0.44
CA1 P00915 4/20 0.43
RORC P51449 2/20 0.41
KCNH3 Q9ULD8 1/20 0.40
ACP1 P24666 2/20 0.40
L3MBTL1 Q9Y468 1/20 0.39
KDM4E B2RXH2 2/20 0.39
LMNA P02545 1/20 0.39
CYP3A4 P08684 1/20 0.39
GAA P10253 1/20 0.39
BLM P54132 1/20 0.39
GFER P55789 1/20 0.39
PMP22 Q01453 1/20 0.39
HDAC3 O15379 1/20 0.38

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 SCHEMBL8441340 0.91 ALDH1A1 (0.48) CA12CA2CA9ALDH1A1MAPT
Sulfuric Acid SCHEMBL2484445 0.91 ALDH1A1 (0.52) CA12CA2CA9ALDH1A1MAPT
Sulfuric Acid SCHEMBL8441342 0.89 CA12 (0.52) CA12CA2CA9ALDH1A1MAPT
Sulfuric Acid SCHEMBL8501318 0.85 CA12 (0.47) CA12CA2CA9ALDH1A1MAPT
Sulfuric Acid SCHEMBL30019534 0.81 CA12 (0.43) CA12CA2CA9ALDH1A1MAPT
SCHEMBL8115 0.81 ALDH1A1 (0.64) ALDH1A1MAPTRECQLMCL1KCNH3
Sulfuric Acid SCHEMBL1605645 0.80 MAPT (0.59) CA12CA2CA9ALDH1A1MAPT
Acetic Acid SCHEMBL9815635 0.80 MAPT (0.52) ALDH1A1MAPTRECQLMCL1RORC
Hydrochloric Acid SCHEMBL1683326 0.79 ALDH1A1 (0.61) ALDH1A1MAPTRECQLMCL1KCNH3
Bromide SCHEMBL28400204 0.79 ALDH1A1 (0.61) ALDH1A1MAPTRECQLMCL1KCNH3

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