SCHEMBL334342

SCHEMBL334342

CC(C)c1ccc(-n2c(CC(=O)O)c(C(=O)O)c3cc(Oc4cccc(Cl)c4)ccc32)cc1

nearest known ligand 0.45

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
USP14 P54578 1/20 0.45
PPARG P37231 7/20 0.44
KDM4E B2RXH2 2/20 0.41
HIF1A Q16665 1/20 0.40
FFAR1 O14842 1/20 0.40
PTGES O14684 1/20 0.40
MEN1 O00255 1/20 0.40
KMT2A Q03164 1/20 0.40
FNTA P49354 1/20 0.38
FNTB P49356 1/20 0.38
PPARA Q07869 1/20 0.38
PTGER4 P35408 2/20 0.38
GAA P10253 1/20 0.37
PTGES2 Q9H7Z7 1/20 0.37

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
SCHEMBL333497 0.92 USP14 (0.44) USP14PPARGKDM4EHIF1AFFAR1
SCHEMBL333959 0.91 USP14 (0.49) USP14PPARGKDM4EHIF1AFFAR1
SCHEMBL503756 0.91 USP14 (0.45) USP14PPARGKDM4EHIF1AFFAR1
SCHEMBL333835 0.90 KDM4E (0.47) USP14KDM4EHIF1AFFAR1PTGES
SCHEMBL334287 0.89 FFAR1 (0.43) USP14PPARGKDM4EHIF1AFFAR1
SCHEMBL333818 0.87 PPARG (0.52) PPARGPPARA
SCHEMBL334235 0.87 BCL2 (0.42) USP14KDM4EPTGESMEN1KMT2A
SCHEMBL334064 0.86 USP14 (0.43) USP14PPARGKDM4EHIF1AFFAR1
SCHEMBL333845 0.86 PPARG (0.42) USP14PPARGKDM4EHIF1AFFAR1
SCHEMBL335371 0.85 USP14 (0.41) USP14KDM4EHIF1AFFAR1PTGES

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8097623-B2 1-Aryl-or heteroaryl-3-aryl-or heteroarylindole-2-carboxylic acids or esters: e.g., 5-(4-tert-Butylphenyl)-1,3-bis(4-isopropoxyphenyl)-indole-2-carboxylic acid; inhibition of the activity of microsomal prostaglandin E synthase-1, leukotriene C4 and/or 5-lipoxygenase-activating protein; analgesics BIOLIPOX AB (SE) 2012-01-17 US disclosed
EP-1841735-B1 INDOLES USEFUL IN THE TREATMENT OF INFLAMMATION BIOLIPOX AB (SE) 2011-03-09 EP disclosed
US-20090076004-A1 Indoles Useful in the Treatment of Inflammation BIOLIPOX AB (SE) 2009-03-19 US disclosed
CN-101142185-A Indoles useful in the treatment of inflammation BIOLIPOX AB (SE) 2008-03-12 CN disclosed
EP-1841735-A1 INDOLES USEFUL IN THE TREATMENT OF INFLAMMATION Biolipox AB (SE) 2007-10-10 EP disclosed
WO-2006077366-A1 INDOLES USEFUL IN THE TREATMENT OF INFLAMMATION BIOLIPOX AB (SE) 2006-07-27 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-20090076004-A1 Indoles Useful in the Treatment of Inflammation IDO1, IDO2, AREG USP14 3873/4885PPARG 2451/4885KDM4E 1104/4885

“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.