Sulfuric Acid

Sulfuric Acid

SCHEMBL8916579

O=S(=O)(O)O.c1ccc(C(c2ccc3ncccc3c2)n2ccnc2)cc1

nearest known ligand 0.55

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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
MAOA known ✓ P21397 1/20 0.52
ADRA1A known ✓ P35348 1/20 0.52
OPRK1 known ✓ P41145 1/20 0.52
CYP19A1 P11511 9/20 0.55
CYP17A1 P05093 2/20 0.52
CYP3A4 P08684 2/20 0.52
MEN1 O00255 1/20 0.52
NR1I2 O75469 1/20 0.52
USP2 O75604 1/20 0.52
ABCB11 O95342 1/20 0.52
ALDH1A1 P00352 1/20 0.52
PLA2G1B P04054 1/20 0.52
TP53 P04637 1/20 0.52
PGR P06401 1/20 0.52
HSP90AA1 P07900 1/20 0.52
MAPT P10636 1/20 0.52
IDO1 P14902 1/20 0.52
HPGD P15428 1/20 0.52
CNR1 P21554 1/20 0.52
HTR2A P28223 1/20 0.52

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
SCHEMBL8920146 0.83 CYP19A1 (0.63) CYP19A1CYP17A1CYP3A4MEN1NR1I2
SCHEMBL9196154 0.79 CYP19A1 (0.69) CYP19A1CYP17A1CYP3A4MEN1NR1I2
SCHEMBL28169691 0.77 CYP19A1 (0.75) CYP19A1CYP17A1CYP3A4MEN1NR1I2
SCHEMBL9195873 0.75 CYP19A1 (0.58) CYP19A1CYP17A1CYP3A4MEN1NR1I2
SCHEMBL738495 0.74 CYP19A1 (1.00) CYP19A1CYP17A1CYP3A4MEN1NR1I2
Water SCHEMBL9728138 0.72 CYP19A1 (0.61) CYP19A1CYP17A1CYP3A4MEN1NR1I2
Bromide SCHEMBL28170216 0.72 CYP19A1 (0.96) CYP19A1CYP17A1CYP3A4MEN1NR1I2
Hydrochloric Acid SCHEMBL28169692 0.72 CYP19A1 (0.96) CYP19A1CYP17A1CYP3A4MEN1NR1I2
SCHEMBL3279238 0.71 CYP19A1 (0.60) CYP19A1CYP17A1CYP3A4MEN1NR1I2
SCHEMBL9664159 0.71 CYP19A1 (0.56) CYP19A1CYP17A1CYP3A4MEN1NR1I2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5612354-A CONTROLLING CELL GROWTH AND DIFFERENTIATION, RETINOIC ACID METABOLISM JANSSEN PHARMACEUTICA N.V. (BE) 1997-03-18 US disclosed
CN-1033752-C (1H-azol-1-ylmethyl) substituted quinoline or quinolinone derivatives JANSSEN PHARMACEUTICA NV (SE) 1997-01-08 CN disclosed
CN-1106005-A A process for preparing (1H-azol-1-ylmethyl) substituted quinoxaline derivatives JANSSEN PHARMACEUTICA NV (BE) 1995-08-02 CN disclosed
CN-1106004-A A process for preparing (1H-azol-1-ylmethyl) substituted quinazoline derivatives JANSSEN PHARMACEUTICA NV (BE) 1995-08-02 CN disclosed
US-5268380-A Therapy for keratinization in mammals JANSSEN PHARMACEUTICA N.V. (BE) 1993-12-07 US disclosed
US-5185346-A Antiandrogenic agents; suppress elimination of retinoids; anticarcinogenic agents HANSSEN PHARMACEUTICA (BE) 1993-02-09 US disclosed
CN-1042912-A (1H-oxazol-1-ylmethyl) substituted quinoline, quinazoline or quinoxaline derivatives JANSSEN PHARMACEUTICA NV (BE) 1990-06-13 CN disclosed