SCHEMBL333868

SCHEMBL333868

CCOC(=O)c1c(CC(=O)O)n(-c2ccc(OC(F)(F)F)cc2)c2ccc(Oc3ccc(Cl)cc3)cc12

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
USP14 P54578 1/20 0.47
ALOX5 P09917 2/20 0.46
PTGES O14684 2/20 0.46
TP53 P04637 4/20 0.45
THRB P10828 2/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
PPARG P37231 2/20 0.44
MAPT P10636 3/20 0.44
MEN1 O00255 4/20 0.43
KMT2A Q03164 4/20 0.43
ELANE P08246 1/20 0.43
NPSR1 Q6W5P4 2/20 0.40
KDM4E B2RXH2 1/20 0.40
ABCC3 O15438 1/20 0.40
ABCC4 O15439 1/20 0.40
ABCB11 O95342 1/20 0.40
MT-CO2 P00403 1/20 0.40
LMNA P02545 1/20 0.40
ALB P02768 1/20 0.40
CYP1A2 P05177 1/20 0.40

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
SCHEMBL333611 0.90 PPARG (0.47) USP14ALOX5PTGESPPARGMAPT
SCHEMBL333844 0.89 MEN1 (0.45) ALOX5PTGESTP53THRBSMN1; SMN2
SCHEMBL333819 0.87 ALOX5 (0.45) USP14ALOX5PTGESTP53THRB
SCHEMBL333732 0.85 PTGES (0.49) USP14ALOX5PTGESTP53THRB
SCHEMBL333651 0.85 USP14 (0.44) USP14ALOX5PTGESTP53THRB
SCHEMBL334059 0.85 ALOX5 (0.45) ALOX5PTGESTP53THRBSMN1; SMN2
SCHEMBL333849 0.84 ALOX5 (0.46) ALOX5TP53THRBSMN1; SMN2PPARG
SCHEMBL333728 0.84 ALOX5 (0.45) ALOX5PTGESTP53THRBSMN1; SMN2
SCHEMBL333879 0.83 PPARG (0.41) USP14PPARGMEN1KMT2AKDM4E
SCHEMBL333571 0.83 TP53 (0.55) USP14PTGESTP53THRBSMN1; SMN2

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 5 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
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 3873/4885ALOX5 1146/4885PTGES 34/4885

“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.