Sulfuric Acid

Sulfuric Acid

SCHEMBL7063446

CCSCCNC(=N)N.O=S(=O)(O)O

nearest known ligand 0.49

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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 19)

geneUniProtsupporting neighboursconfidence
ALOX15 P16050 1/20 0.46
TSHR P16473 4/20 0.40
HIF1A Q16665 1/20 0.40
CYP2D6 P10635 2/20 0.39
CYP2C19 P33261 2/20 0.39
BLM P54132 2/20 0.39
KDM4E B2RXH2 1/20 0.39
NPSR1 Q6W5P4 1/20 0.39
PKM P14618 1/20 0.35
CYP1A2 P05177 2/20 0.34
MEN1 O00255 1/20 0.34
KMT2A Q03164 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
LMNA P02545 1/20 0.34
NOS3 P29474 1/20 0.31
NOS1 P29475 1/20 0.31
NOS2 P35228 1/20 0.31
ALDH1A1 P00352 1/20 0.30
TDP1 Q9NUW8 1/20 0.30

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
SCHEMBL9697092 0.90
Sulfuric Acid SCHEMBL7064849 0.81 ALOX15 (0.49) ALOX15TSHRHIF1ACYP2D6CYP2C19
SCHEMBL17472392 0.79 CYP1A2 (0.41) ALOX15TSHRHIF1ACYP2D6CYP2C19
Sulfuric Acid SCHEMBL10930716 0.78 ALOX15 (0.53) ALOX15TSHRHIF1ACYP2D6CYP2C19
Arcaine SCHEMBL1999196 0.75 ALOX15 (0.70) ALOX15TSHRHIF1ACYP2D6CYP2C19
Sulfuric Acid SCHEMBL11557628 0.75 ALOX15 (0.59) ALOX15CYP1A2MEN1KMT2ASMN1; SMN2
Sulfuric Acid SCHEMBL5457417 0.75 ALOX15 (0.59) ALOX15CYP1A2MEN1KMT2ASMN1; SMN2
SCHEMBL10719447 0.75 ALOX15 (0.46) ALOX15TSHRHIF1ACYP2D6CYP2C19
Sulfuric Acid SCHEMBL6049589 0.73 ALOX15 (0.47) ALOX15CYP2D6CYP2C19BLMKDM4E
Sulfuric Acid SCHEMBL11815400 0.73 ALOX15 (0.47) ALOX15CYP2D6CYP2C19BLMKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0814792-B1 MERCAPTO AND SELENO DERIVATIVES AS INHIBITORS OF NITRIC OXIDE SYNTHASE CHILDRENS HOSP MEDICAL CENTER (US) 2003-05-28 EP disclosed
US-5985917-A ANTITUMOR AGENTS AND ENZYME INHIBITORS CHILDREN'S HOSPITAL MEDICAL CENTER (US) 1999-11-16 US disclosed
US-5952385-A Mercapto derivatives as inhibitors of nitric oxide synthase CHILDREN'S HOSPITAL MEDICAL CENTER (US) 1999-09-14 US disclosed
US-5929063-A SELECTIVELY INHIBITS THE INDUCIBLE ISOFORM TO PREVENT OVER-INHIBITION; FOR DISORDERS WHERE THE ENZYME PLAYS A ROLE, E.G SYSTEMIC HYPOTENSION, SEPTIC SHOCK AND CYTOKINE THERAPY CHILDREN'S HOSPITAL MEDICAL CENTER (US) 1999-07-27 US disclosed
EP-0814792-A1 MERCAPTO AND SELENO DERIVATIVES AS INHIBITORS OF NITRIC OXIDE SYNTHASE CHILDREN'S HOSPITAL MEDICAL CENTER (US) 1998-01-07 EP disclosed
WO-1997045108-A1 GUANIDINO DERIVATIVES AS INHIBITORS OF THE CYTOTOXIC EFFECT OF PEROXYNITRITE CHILDREN'S HOSPITAL MEDICAL CENTER (US) 1997-12-04 WO disclosed
US-5674907-A Mercapto derivatives as inhibitors of nitric oxide synthase CHILDREN'S HOSPITAL MEDICAL CENTER (US) 1997-10-07 US disclosed
WO-1996030007-A1 MERCAPTO AND SELENO DERIVATIVES AS INHIBITORS OF NITRIC OXIDE SYNTHASE CHILDREN'S HOSPITAL MEDICAL CENTER (US) 1996-10-03 WO disclosed