SCHEMBL2540490

SCHEMBL2540490

CC(C)(C)c1ccc(COc2ccc(-c3cccc(OC(F)(F)F)c3)cc2CCC(=O)O)cc1

nearest known ligand 0.48

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
FFAR4 Q5NUL3 8/20 0.48
FFAR1 O14842 7/20 0.48
MME P08473 1/20 0.48
SLC13A5 Q86YT5 1/20 0.47
NR4A1 P22736 1/20 0.46
NR4A2 P43354 1/20 0.46
NR4A3 Q92570 1/20 0.46
PTGER4 P35408 3/20 0.45
PTGER3 P43115 3/20 0.45
PTGER1 P34995 2/20 0.45
PTGER2 P43116 2/20 0.45
NPSR1 Q6W5P4 1/20 0.44
S1PR1 P21453 1/20 0.42
CTSA P10619 1/20 0.42
FFAR2 O15552 1/20 0.41

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
SCHEMBL2537299 0.93 FFAR4 (0.47) FFAR4FFAR1MMESLC13A5PTGER4
SCHEMBL2536390 0.91 FFAR4 (0.49) FFAR4FFAR1NR4A2PTGER4PTGER3
SCHEMBL2535066 0.91 FFAR4 (0.49) FFAR4FFAR1NR4A2PTGER4PTGER3
SCHEMBL2534023 0.87 PTGER4 (0.55) FFAR4FFAR1NR4A1NR4A2NR4A3
SCHEMBL2536062 0.86 RXRA (0.53) FFAR4FFAR1NR4A1NR4A2NR4A3
SCHEMBL2539389 0.85 FFAR4 (0.51) FFAR4FFAR1PTGER4PTGER3PTGER1
SCHEMBL2537526 0.85 FFAR1 (0.58) FFAR4FFAR1MMESLC13A5PTGER4
SCHEMBL2533427 0.85 FFAR4 (0.51) FFAR4FFAR1PTGER4PTGER3PTGER1
SCHEMBL2532590 0.85 FFAR1 (0.58) FFAR4FFAR1MMESLC13A5PTGER4
SCHEMBL2535115 0.85 PTGER4 (0.53) FFAR4FFAR1MMEPTGER4PTGER3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8044236-B2 Inhibitors against plasminogen activator inhibitor-1 (PAI-1); anticoagulants; 2-(aryl or aralkyloxy-)-5-(aryl)phenyl}acetic acid (or derivatives of propionic acid, propenoic acid, N-oxamic acid or 1H-tetrazol-5-yl); occlusion, stenosis; low molecular weight; gene expression inhibition INSTITUTE OF MEDICINAL MOLECULAR DESIGN, INC. (JP) 2011-10-25 US disclosed
EP-2080751-A1 CARBOXYLIC ACID DERIVATIVE Institute of Medicinal Molecular Design, Inc. (JP) 2009-07-22 EP disclosed
US-20080275116-A1 Carboxilic acid derivatives INSTITUTE OF MEDICINAL MOLECULAR DESIGN, INC. (JP) 2008-11-06 US 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-20080275116-A1 Carboxilic acid derivatives SERPINE1, CTRL, SERPINC1 FFAR4 2537/4885FFAR1 710/4885MME 248/4885

“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.