Sulfuric Acid

Sulfuric Acid

SCHEMBL8640969

Nc1ccc(Oc2cccc(Oc3ccc(N)cc3)c2)cc1.O=S(=O)(O)O

nearest known ligand 0.77

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
MAOA known ✓ P21397 2/20 0.57
MAOB known ✓ P27338 2/20 0.52
ALDH1A1 P00352 5/20 0.77
SMN1; SMN2 Q16637 3/20 0.77
MEN1 O00255 2/20 0.77
KMT2A Q03164 2/20 0.77
MAPT P10636 2/20 0.77
MITF O75030 1/20 0.77
GAA P10253 1/20 0.77
GFER P55789 1/20 0.77
NLRP1 Q9C000 1/20 0.77
NOD2 Q9HC29 1/20 0.77
NPC1 O15118 1/20 0.56
RAB9A P51151 1/20 0.56
NLRP3 Q96P20 1/20 0.56
CYP3A4 P08684 1/20 0.54
TSHR P16473 1/20 0.54
TDP1 Q9NUW8 1/20 0.54
FURIN P09958 2/20 0.50
F2 P00734 1/20 0.50

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 SCHEMBL8643727 0.93 ALDH1A1 (0.66) ALDH1A1SMN1; SMN2MEN1KMT2AMAPT
SCHEMBL63594 0.88 ALDH1A1 (1.00) ALDH1A1SMN1; SMN2MEN1KMT2AMAPT
SCHEMBL1271678 0.88 ALDH1A1 (1.00) ALDH1A1SMN1; SMN2MEN1KMT2AMAPT
SCHEMBL6289307 0.88 ALDH1A1 (1.00) ALDH1A1SMN1; SMN2MEN1KMT2AMAPT
SCHEMBL1270594 0.88 ALDH1A1 (1.00) ALDH1A1SMN1; SMN2MEN1KMT2AMAPT
SCHEMBL562469 0.88 ALDH1A1 (1.00) ALDH1A1SMN1; SMN2MEN1KMT2AMAPT
SCHEMBL4092959 0.88 ALDH1A1 (1.00) ALDH1A1SMN1; SMN2MEN1KMT2AMAPT
SCHEMBL6290330 0.88 ALDH1A1 (1.00) ALDH1A1SMN1; SMN2MEN1KMT2AMAPT
SCHEMBL22289568 0.88 ALDH1A1 (1.00) ALDH1A1SMN1; SMN2MEN1KMT2AMAPT
SCHEMBL6290623 0.88 ALDH1A1 (1.00) ALDH1A1SMN1; SMN2MEN1KMT2AMAPT

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-5821320-A MIXING AROMATIC DIAMINE DIHYDROCHLORIDE OR SULFATE WITH AROMATIC ACID DIANHYDRIDE, HEATING TO DEHYDRATE AND CONDENSE PETROLEUM ENERGY CENTER (JP) 1998-10-13 US disclosed