SCHEMBL6472900

SCHEMBL6472900

CSc1ccc(C=C(C(=O)O)C2=C(C)Cc3ccc(F)cc32)cc1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ AKR1C3 P42330 5/20 0.47
▸ AKR1C2 P52895 4/20 0.47
▸ AKR1C1 Q04828 4/20 0.47
▸ PPARG P37231 3/20 0.44
▸ PTGS2 P35354 3/20 0.44
▸ PTGS1 P23219 2/20 0.44
▸ TDP1 Q9NUW8 2/20 0.44
▸ EGFR P00533 1/20 0.44
▸ CYP1A2 P05177 1/20 0.44
▸ ADORA3 P0DMS8 1/20 0.44
▸ MAPT P10636 1/20 0.44
▸ DRD1 P21728 1/20 0.44
▸ MAPK1 P28482 1/20 0.44
▸ OPRM1 P35372 1/20 0.44
▸ PSEN1 P49768 1/20 0.44
▸ PSEN2 P49810 1/20 0.44
▸ APH1B Q8WW43 1/20 0.44
▸ NCSTN Q92542 1/20 0.44
▸ APH1A Q96BI3 1/20 0.44
▸ PSENEN Q9NZ42 1/20 0.44

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
SCHEMBL6472251 1.00 AKR1C3 (0.47) AKR1C3AKR1C2AKR1C1PPARGPTGS2
SCHEMBL8428502 0.86 PTGS2 (0.38) AKR1C3AKR1C2AKR1C1PPARGPTGS2
SCHEMBL8797000 0.85 AKR1C3 (0.45) AKR1C3AKR1C2AKR1C1PTGS2PTGS1
SCHEMBL2219869 0.83 AKR1C3 (0.57) AKR1C3AKR1C2AKR1C1PTGS2TDP1
SCHEMBL8521003 0.83 PTGS2 (0.45) AKR1C3AKR1C2AKR1C1PTGS2
SCHEMBL8506321 0.83 PTGS2 (0.38) AKR1C3AKR1C2AKR1C1PPARGPTGS2
SCHEMBL2223120 0.83 PTGS2 (0.38) AKR1C3AKR1C2AKR1C1PPARGPTGS2
SCHEMBL5138929 0.81 AKR1C3 (0.43) AKR1C3AKR1C2AKR1C1PTGS2TDP1
SCHEMBL8430248 0.75 CES2 (0.35) CYP1A2MAPTPOLBALDH1A1MEN1
SCHEMBL7840253 0.73 AKR1C3 (0.56) AKR1C3AKR1C2AKR1C1PPARGPTGS2

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-2882426-A1 METHODS AND PHARMACEUTICAL COMPOSITIONS FOR TREATMENT OF CYSTIC FIBROSIS Institut National de la Santé et de la Recherche Médicale (INSERM) (FR) 2015-06-17 — — EP disclosed
WO-2014026959-A1 METHODS AND PHARMACEUTICAL COMPOSITIONS FOR TREATMENT OF CYSTIC FIBROSIS INSERM (Institut National de la Santé et de la Recherche Médicale) (FR) 2014-02-20 — — WO disclosed
WO-2005068411-A1 PROCESS FOR THE PREPARATION OF 6-FLUORO-2-METHYL-1-INDANONE ZAMBON GROUP S.P.A. (IT) 2005-07-28 — — WO disclosed
WO-1998013073-A9 METHODS OF ENHANCING THE THERAPEUTIC ACTIVITY OF NSAIDs AND COMPOSITIONS OF ZWITTERIONIC PHOSPHOLIPIDS USEFUL THEREIN — 1998-08-06 — — WO disclosed
EP-0805684-A4 METHODS OF ENHANCING THE THERAPEUTIC ACTIVITY OF NSAIDS AND COMPOSITIONS OF ZWITTERIONIC PHOSPHOLIPIDS USEFUL THEREIN UNIV TEXAS (US) 1998-08-05 — — EP disclosed
EP-0805684-A2 METHODS OF ENHANCING THE THERAPEUTIC ACTIVITY OF NSAIDS AND COMPOSITIONS OF ZWITTERIONIC PHOSPHOLIPIDS USEFUL THEREIN THE BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1997-11-12 — — EP disclosed
WO-1996022780-A1 METHODS OF ENHANCING THE THERAPEUTIC ACTIVITY OF NSAIDS AND COMPOSITIONS OF ZWITTERIONIC PHOSPHOLIPIDS USEFUL THEREIN THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 1996-08-01 — — WO disclosed
EP-0206241-A1 Process for the preparation of cis-5-fluoro-2-methyl-1-(4-methylthiobenzylidene)-indene-3-acetic acid ZAMBON S.p.A. (IT) 1986-12-30 — — EP disclosed
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