SCHEMBL333880

SCHEMBL333880

CCOC(=O)c1c(CC(=O)O)n(-c2ccc(OC(C)C)cc2)c2ccc(Oc3ccc(CCl)cn3)cc12

nearest known ligand 0.41

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.41
THRB P10828 2/20 0.41
TP53 P04637 5/20 0.41
PTGES O14684 1/20 0.39
MEN1 O00255 5/20 0.39
KMT2A Q03164 5/20 0.39
MAPT P10636 4/20 0.39
POLB P06746 1/20 0.39
ATM Q13315 1/20 0.38
RAD52 P43351 2/20 0.38
KDM4E B2RXH2 1/20 0.38
HTT P42858 1/20 0.38

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
SCHEMBL334156 0.94 TP53 (0.41) SMN1; SMN2THRBTP53PTGESMEN1
SCHEMBL1407633 0.91 ACACB (0.38) PTGESMEN1KMT2AKDM4E
SCHEMBL333326 0.89 ALOX5 (0.41) SMN1; SMN2THRBTP53PTGESMEN1
SCHEMBL333797 0.89 SMN1; SMN2 (0.42) SMN1; SMN2THRBTP53PTGESMEN1
SCHEMBL334190 0.87 SCN9A (0.45) SMN1; SMN2THRBTP53MEN1KMT2A
SCHEMBL334065 0.83 ALOX5 (0.41) SMN1; SMN2THRBTP53PTGESMEN1
SCHEMBL335032 0.83 TP53 (0.41) SMN1; SMN2THRBTP53MEN1KMT2A
SCHEMBL333746 0.81 SCN9A (0.45) SMN1; SMN2THRBTP53MAPTPOLB
SCHEMBL333965 0.80 TP53 (0.45) SMN1; SMN2THRBTP53MEN1KMT2A
SCHEMBL4223256 0.80 PTGES (0.46) SMN1; SMN2THRBTP53PTGESMEN1

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 SMN1; SMN2 3963/4885THRB 575/4885TP53 738/4885

“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.