SCHEMBL7084859

SCHEMBL7084859

CS(=O)(=O)c1ccc(-c2nc(C(F)(F)F)[nH]c2-c2ccccc2)cc1

nearest known ligand 0.67

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
PTGS2 P35354 10/20 0.67
PTGS1 P23219 9/20 0.67
ESR1 P03372 1/20 0.65
ESR2 Q92731 1/20 0.65
ALDH1A1 P00352 2/20 0.56
HPGD P15428 1/20 0.56
ALOX5 P09917 1/20 0.50
CSNK1A1 P48729 1/20 0.50
CSNK1D P48730 1/20 0.50
CSNK1E P49674 1/20 0.50
MAPK11 Q15759 1/20 0.50
MAPK14 Q16539 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
CSNK1A1L Q8N752 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
SCHEMBL213705 0.90 PTGS2 (0.70) PTGS2PTGS1ESR1ESR2ALDH1A1
SCHEMBL7084237 0.90 PTGS2 (0.55) PTGS2PTGS1ESR1ESR2ALDH1A1
SCHEMBL7088103 0.90 PTGS1 (0.55) PTGS2PTGS1ESR1ESR2ALDH1A1
SCHEMBL5698511 0.90 PTGS2 (0.70) PTGS2PTGS1ESR1ESR2ALDH1A1
SCHEMBL7088524 0.88 PTGS1 (0.68) PTGS2PTGS1ESR1ESR2ALDH1A1
SCHEMBL7084867 0.88 PTGS2 (0.54) PTGS2PTGS1ESR1ESR2ALDH1A1
SCHEMBL7088151 0.88 PTGS1 (0.69) PTGS2PTGS1ALDH1A1HPGD
SCHEMBL7088250 0.88 PTGS2 (0.52) PTGS2PTGS1ESR1ESR2ALDH1A1
SCHEMBL11090108 0.88 PTGS1 (0.62) PTGS2PTGS1ESR1ESR2ALDH1A1
SCHEMBL10878849 0.88 PTGS1 (0.62) PTGS2PTGS1ESR1ESR2ALDH1A1

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102603646-B Synthesis method of 4-[4-(methylsulfonyl)phenyl]-5-phenyl-2-(trifluoromethyl)-1H-imidazole UNIV ZHEJIANG 2014-07-02 CN claimed
CN-102603646-A Synthesis method of 4-[4-(methylsulfonyl)phenyl]-5-phenyl-2-(trifluoromethyl)-1H-imidazole UNIV ZHEJIANG 2012-07-25 CN claimed
US-20030050330-A1 4,5-subtstituted imdazolyl compounds for the treatment of inflammation G.D. SEARLE & CO. 2003-03-13 US claimed
EP-0772601-B1 4,5-SUBSTITUTED IMIDAZOLYL COMPOUNDS FOR THE TREATMENT OF INFLAMMATION SEARLE & CO (US) 2002-09-18 EP claimed
US-6426360-B1 ANTIARTHRITIC AGENTS G D SEARLE & CO. 2002-07-30 US claimed
EP-1211244-A2 4,5-substitued imidazolyl compounds for the treatment of inflammation G.D. Searle & Co. (US) 2002-06-05 EP claimed
EP-0772601-A1 4,5-SUBSTITUTED IMIDAZOLYL COMPOUNDS FOR THE TREATMENT OF INFLAMMATION G.D. SEARLE & CO. (US) 1997-05-14 EP claimed
WO-1996003387-A1 4,5-SUBSTITUTED IMIDAZOLYL COMPOUNDS FOR THE TREATMENT OF INFLAMMATION G.D. SEARLE & CO. (US) 1996-02-08 WO claimed
CN-102603646-B Synthesis method of 4-[4-(methylsulfonyl)phenyl]-5-phenyl-2-(trifluoromethyl)-1H-imidazole UNIV ZHEJIANG 2014-07-02 CN disclosed
CN-102603646-B Synthesis method of 4-[4-(methylsulfonyl)phenyl]-5-phenyl-2-(trifluoromethyl)-1H-imidazole UNIV ZHEJIANG 2014-07-02 CN disclosed
CN-102603646-B Synthesis method of 4-[4-(methylsulfonyl)phenyl]-5-phenyl-2-(trifluoromethyl)-1H-imidazole UNIV ZHEJIANG 2014-07-02 CN disclosed
CN-102603646-A Synthesis method of 4-[4-(methylsulfonyl)phenyl]-5-phenyl-2-(trifluoromethyl)-1H-imidazole UNIV ZHEJIANG 2012-07-25 CN disclosed
CN-102603646-A Synthesis method of 4-[4-(methylsulfonyl)phenyl]-5-phenyl-2-(trifluoromethyl)-1H-imidazole UNIV ZHEJIANG 2012-07-25 CN disclosed
CN-102603646-A Synthesis method of 4-[4-(methylsulfonyl)phenyl]-5-phenyl-2-(trifluoromethyl)-1H-imidazole UNIV ZHEJIANG 2012-07-25 CN disclosed
EP-0772601-B1 4,5-SUBSTITUTED IMIDAZOLYL COMPOUNDS FOR THE TREATMENT OF INFLAMMATION SEARLE & CO (US) 2002-09-18 EP disclosed
US-6426360-B1 ANTIARTHRITIC AGENTS G D SEARLE & CO. 2002-07-30 US disclosed
EP-1211244-A2 4,5-substitued imidazolyl compounds for the treatment of inflammation G.D. Searle & Co. (US) 2002-06-05 EP disclosed
EP-0772601-A1 4,5-SUBSTITUTED IMIDAZOLYL COMPOUNDS FOR THE TREATMENT OF INFLAMMATION G.D. SEARLE & CO. (US) 1997-05-14 EP disclosed
US-5620999-A ANTIARTHRITIC, ANALGESIC AND ANTIPYRATIC AGENT G.D. SEARLE & CO. 1997-04-15 US disclosed
WO-1996003387-A1 4,5-SUBSTITUTED IMIDAZOLYL COMPOUNDS FOR THE TREATMENT OF INFLAMMATION G.D. SEARLE & CO. (US) 1996-02-08 WO 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 (1 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-20030050330-A1 4,5-subtstituted imdazolyl compounds for the treatment of inflammation AHR, HACL2, IRAK2 PTGS2 122/4885PTGS1 114/4885ESR1 3743/4885

“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.