Sulfuric Acid

Sulfuric Acid

SCHEMBL7056944

Cc1cccc[n+]1CCO.Cc1cccc[n+]1CCO.O=S(=O)([O-])[O-]

nearest known ligand 0.53

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Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

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
POLB P06746 3/20 0.53
SMN1; SMN2 Q16637 3/20 0.53
NPC1 O15118 1/20 0.53
RAB9A P51151 1/20 0.53
KMT2A Q03164 3/20 0.39
ALDH1A1 P00352 4/20 0.36
KDM4E B2RXH2 4/20 0.36
RXFP1 Q9HBX9 1/20 0.36
PABPC1 P11940 1/20 0.35
THRB P10828 1/20 0.35
MEN1 O00255 2/20 0.35
LMNA P02545 1/20 0.35
MMP14 P50281 1/20 0.35
GAA P10253 1/20 0.34
HPGD P15428 1/20 0.34
CYP2C19 P33261 1/20 0.34
MAPT P10636 1/20 0.32
CA12 O43570 1/20 0.31
CA1 P00915 1/20 0.31
CA2 P00918 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
SCHEMBL1827048 0.89 POLB (0.64) POLBSMN1; SMN2NPC1RAB9AKMT2A
SCHEMBL29724058 0.89 POLB (0.64) POLBSMN1; SMN2NPC1RAB9AKMT2A
Hydrochloric Acid SCHEMBL7599736 0.87 POLB (0.62) POLBSMN1; SMN2NPC1RAB9AKMT2A
Bromide SCHEMBL11433371 0.87 POLB (0.68) POLBSMN1; SMN2NPC1RAB9AKMT2A
SCHEMBL7056036 0.87 POLB (0.44) POLBSMN1; SMN2NPC1RAB9AKMT2A
Sulfuric Acid SCHEMBL2185375 0.81 CYP2D6 (0.34) POLBSMN1; SMN2NPC1RAB9AKMT2A
SCHEMBL29252527 0.79 SMN1; SMN2 (0.53) POLBSMN1; SMN2NPC1RAB9AKMT2A
Sulfuric Acid SCHEMBL781947 0.79 NPC1 (0.67) POLBSMN1; SMN2NPC1RAB9AKMT2A
Sulfuric Acid SCHEMBL781847 0.79 NPC1 (0.67) POLBSMN1; SMN2NPC1RAB9AKMT2A
SCHEMBL21523383 0.78 POLB (0.61) POLBSMN1; SMN2NPC1RAB9AKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0776888-B1 Process for the preparation of beta-Hydrosyalkylpicolinium salts and picolinium salts as intermediates for the prepation of cationic dyes BAYER AG (DE) 2003-05-14 EP disclosed
EP-1264825-A1 Beta-Hydroxyalkylpicoliniumsalts Bayer Aktiengesellschaft (DE) 2002-12-11 EP disclosed
US-5840902-A REACTING PICOLINE WITH ALKYLENE OXIDE IN PRESENCE OF ACID IN WATER OR MIXTURE OF WATER AND POLAR SOLVENT BAYER AKTIENGESELLSCHAFT (DE) 1998-11-24 US disclosed
EP-0776888-A2 Process for the preparation of beta-Hydrosyalkylpicolinium salts and picolinium salts as intermediates for the prepation of cationic dyes BAYER AG (DE) 1997-06-04 EP disclosed