SCHEMBL634162

SCHEMBL634162

Nc1c(S(=O)(=O)O)cc(Nc2ccc(S(N)(=O)=O)cc2)c2c1C(=O)c1ccccc1C2=O

nearest known ligand 0.80

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GNG2 P59768 5/20 0.80
GNB1 P62873 5/20 0.80
PHLPP2 Q6ZVD8 2/20 0.79
CYP1A2 P05177 2/20 0.79
CYP2C9 P11712 2/20 0.79
ALOX15 P16050 2/20 0.79
HSD17B10 Q99714 2/20 0.79
ALDH1A1 P00352 1/20 0.79
CYP3A4 P08684 1/20 0.79
HPGD P15428 1/20 0.79
MAPK1 P28482 1/20 0.79
CYP2C19 P33261 1/20 0.79
HIF1A Q16665 1/20 0.79
P2RY12 Q9H244 6/20 0.67
P2RY4 P51582 8/20 0.67
P2RY2 P41231 6/20 0.66
P2RY6 Q15077 4/20 0.66
ENTPD1 P49961 2/20 0.66
MET P08581 2/20 0.65
HGF P14210 2/20 0.65

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
SCHEMBL10708708 0.93 GNG2 (0.84) GNG2GNB1PHLPP2CYP1A2CYP2C9
SCHEMBL13021512 0.93 GNG2 (0.92) GNG2GNB1PHLPP2CYP1A2CYP2C9
SCHEMBL3026032 0.92 GNG2 (0.82) GNG2GNB1PHLPP2CYP1A2CYP2C9
SCHEMBL11415305 0.89 GNG2 (0.78) GNG2GNB1PHLPP2CYP1A2CYP2C9
SCHEMBL13213975 0.89 GNG2 (0.86) GNG2GNB1PHLPP2CYP1A2CYP2C9
SCHEMBL2778161 0.89 GNG2 (1.00) GNG2GNB1PHLPP2CYP1A2CYP2C9
SCHEMBL29354288 0.89 GNG2 (1.00) GNG2GNB1PHLPP2CYP1A2CYP2C9
SCHEMBL791019 0.89 GNG2 (0.85) GNG2GNB1PHLPP2CYP1A2CYP2C9
SCHEMBL29357302 0.89 GNG2 (0.85) GNG2GNB1PHLPP2CYP1A2CYP2C9
SCHEMBL2781947 0.88 GNG2 (1.00) GNG2GNB1PHLPP2CYP1A2CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7238718-B2 Method for treating myolytic disease and method for screening antimyolytic agent OSAKA BIOSCIENCE INSTITUTE (JP) 2007-07-03 US claimed
US-20050272767-A1 Method for treating myolytic disease and method for screening antimyolytic agent OSAKA BIOSCIENCE INSTITUTE AND RIKEN (JP) 2005-12-08 US claimed
US-20050227984-A1 Drugs for improving the prognosis of brain injury and a method of screening the same TAIHO PHARMACEUTICAL CO., LTD. (JP) 2005-10-13 US claimed
EP-1535629-A1 DRUGS FOR IMPROVING THE PROGNOSIS OF BRAIN INJURY AND A METHOD OF SCREENING THE SAME Japan Science and Technology Agency (JP) 2005-06-01 EP claimed
US-8568967-B2 Method for diagnosis of severity and prediction of recurrence in eosinophilic inflammatory disease TAIHO PHARMACEUTICAL CO., LTD. (JP) 2013-10-29 US disclosed
EP-1882937-B1 METHOD FOR DIAGNOSIS OF SEVERITY AND PREDICTION OF RECURRENCE IN EOSINOPHILIC INFLAMMATORY DISEASE TAIHO PHARMACEUTICAL CO LTD (JP) 2012-02-22 EP disclosed
US-20100138937-A1 Method for diagnosis of severity and prediction of recurrence in eosinophilic inflammatory disease AROS ELECTRONICS AB (SE) 2010-06-03 US disclosed
EP-1882937-A1 METHOD FOR DIAGNOSIS OF SEVERITY AND PREDICTION OF RECURRENCE IN EOSINOPHILIC INFLAMMATORY DISEASE TAIHO PHARMACEUTICAL COMPANY LIMITED (JP) 2008-01-30 EP disclosed
US-7238718-B2 Method for treating myolytic disease and method for screening antimyolytic agent OSAKA BIOSCIENCE INSTITUTE (JP) 2007-07-03 US disclosed
US-20050272767-A1 Method for treating myolytic disease and method for screening antimyolytic agent OSAKA BIOSCIENCE INSTITUTE AND RIKEN (JP) 2005-12-08 US disclosed
EP-1598065-A2 Drugs for improving prognosis of brain injury Japan Science and Technology Agency (JP) 2005-11-23 EP disclosed
US-20050227984-A1 Drugs for improving the prognosis of brain injury and a method of screening the same TAIHO PHARMACEUTICAL CO., LTD. (JP) 2005-10-13 US disclosed
US-20050222235-A1 Drugs for improving the prognosis of brain injury and a method of screening the same SHIONOGI & CO., LTD. (JP) 2005-10-06 US disclosed
EP-1535629-A1 DRUGS FOR IMPROVING THE PROGNOSIS OF BRAIN INJURY AND A METHOD OF SCREENING THE SAME Japan Science and Technology Agency (JP) 2005-06-01 EP disclosed
JP-2004002248-A HUMAN-ORIGINATED PROSTAGRANDIN-SYNTHESIZING ENZYME INHIBITOR JAPAN SCIENCE & TECHNOLOGY CORP 2004-01-08 JP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050222235-A1 Drugs for improving the prognosis of brain injury and a method of screening the same HPGDS, PTGDR, PTGDR2 GNG2 1783/4885GNB1 1888/4885PHLPP2 3324/4885
US-20050227984-A1 Drugs for improving the prognosis of brain injury and a method of screening the same HPGDS, PTGDR, PTGDR2 GNG2 1783/4885GNB1 1888/4885PHLPP2 3324/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.