Sulfuric Acid

Sulfuric Acid

SCHEMBL9067178

NCc1ccc(O)cc1.O=S(=O)(O)O

nearest known ligand 0.76

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
SLC6A2 known ✓ P23975 2/20 0.50
ADRA2A known ✓ P08913 1/20 0.50
ABAT P80404 1/20 0.76
CA2 P00918 4/20 0.52
CA1 P00915 3/20 0.52
CA12 O43570 2/20 0.52
CA9 Q16790 2/20 0.52
CA4 P22748 1/20 0.52
CA6 P23280 1/20 0.52
CA5A P35218 1/20 0.52
CA7 P43166 1/20 0.52
CA14 Q9ULX7 1/20 0.52
CA5B Q9Y2D0 1/20 0.52
TAAR1 Q96RJ0 3/20 0.50
KDM4E B2RXH2 2/20 0.50
ALDH1A1 P00352 2/20 0.50
HTR1A P08908 1/20 0.50
CYP2C19 P33261 1/20 0.50
HTR3A P46098 1/20 0.50
BACE1 P56817 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
SCHEMBL27534980 0.91 ABAT (0.70) ABATCA2CA1CA12CA9
SCHEMBL63123 0.87
SCHEMBL20696075 0.85 ABAT (0.94) ABATCA2TAAR1KDM4EALDH1A1
SCHEMBL27558427 0.85
Water SCHEMBL8381326 0.85 ABAT (0.94) ABATCA2TAAR1KDM4EALDH1A1
Hydrochloric Acid SCHEMBL920435 0.85 ABAT (0.94) ABATTAAR1KDM4EALDH1A1SLC6A2
Bromide SCHEMBL3539884 0.85 ABAT (0.94) ABATCA2TAAR1KDM4EALDH1A1
SCHEMBL27827976 0.85 ABAT (0.67) ABATCA2CA1CA12CA9
Tyramine SCHEMBL236651 0.82 TAAR1 (0.78) ABATCA2CA1CA12CA9
Tyramine SCHEMBL7044901 0.82 TAAR1 (0.78) ABATCA2CA1CA12CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5534565-A DICYANDIAMIDE DERIVATIVES FOR LAMINATES ALLIEDSIGNAL INC. (US) 1996-07-09 US disclosed
EP-0540644-B1 SUBSTITUTED CYANOGUANIDINES AS CURING AGENTS FOR EPOXY RESINS ALLIED SIGNAL INC (US) 1995-08-23 EP disclosed
US-5387656-A Soluble in various solvents; do not require the use of undesirable solvents necessary with cyanoguanidine itself ALLIEDSIGNAL INC. (US) 1995-02-07 US disclosed
WO-1994014866-A1 SOLVENT FREE EPOXY RESIN COMPOSITIONS ALLIEDSIGNAL, INC. (US) 1994-07-07 WO disclosed
EP-0540644-A1 SUBSTITUTED CYANOGUANIDINES AS CURING AGENTS FOR EPOXY RESINS. ALLIED SIGNAL INC (US) 1993-05-12 EP disclosed
WO-1992001726-A1 SUBSTITUTED CYANOGUANIDINES AS CURING AGENTS FOR EPOXY RESINS ALLIED-SIGNAL INC. (US) 1992-02-06 WO disclosed