SCHEMBL1270026

SCHEMBL1270026

CCCCOc1cc(CCC(=O)O)ccc1CCCc1ccc(OCC)c(OC)c1

nearest known ligand 0.51

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
HDAC1 Q13547 3/20 0.51
HDAC2 Q92769 3/20 0.51
APP P05067 1/20 0.49
PPARA Q07869 2/20 0.49
LTA4H P09960 1/20 0.48
LTB4R Q15722 1/20 0.48
FFAR4 Q5NUL3 1/20 0.47
CALM1 P0DP23 2/20 0.46
PPARG P37231 1/20 0.46
RXRA P19793 1/20 0.46
KDM4E B2RXH2 1/20 0.45
TP53 P04637 1/20 0.45

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
SCHEMBL1270107 0.97 HDAC1 (0.53) HDAC1HDAC2APPPPARALTA4H
SCHEMBL3405574 0.94 HDAC1 (0.52) HDAC1HDAC2APPPPARALTA4H
SCHEMBL1269389 0.90 HDAC1 (0.52) HDAC1HDAC2APPLTA4HCALM1
SCHEMBL1269120 0.90 APP (0.61) HDAC1HDAC2APPFFAR4
SCHEMBL1270401 0.89 HDAC1 (0.49) HDAC1HDAC2APPLTA4HCALM1
SCHEMBL3406479 0.88 LTB4R (0.47) PPARALTB4RPPARGRXRA
SCHEMBL1270374 0.88 CYP3A4 (0.58) LTA4HLTB4RRXRA
SCHEMBL1270236 0.88 HDAC1 (0.46) HDAC1HDAC2APPPPARALTA4H
SCHEMBL1268950 0.88 LTA4H (0.47) HDAC1HDAC2APPPPARALTA4H
SCHEMBL1270074 0.87 HDAC1 (0.55) HDAC1HDAC2APPLTA4H

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7879907-B2 Peroxisome Proliferator-Activated Receptor (PPAR) activators such as 3-{4-[3-(4-benzyloxy-3-methoxyphenyl)propyl]-3-butoxyphenyl}propanoic acid, used in dermatology, cosmetics, cardiovascular diseases, immunology and/or lipid metabolism GALDERMA RESEARCH & DEVELOPMENT (FR) 2011-02-01 US claimed
EP-2155662-B1 NOVEL DERIVATIVES OF 3-PHENYL PROPANOIC ACID ACTIVATING PPAR-TYPE RECEPTORS, METHOD FOR PREPARING SAME AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS GALDERMA RES & DEV (FR) 2010-12-01 EP claimed
US-20100158843-A1 NOVEL 3-PHENYLPROPANOIC COMPOUND ACTIVATORS OF RECEPTORS OF PPAR TYPE AND PHARMACEUTICAL/COSMETIC COMPOSITIONS COMPRISED THEREOF GALDERMA RESEARCH & DEVELOPMENT (FR) 2010-06-24 US claimed
US-7879907-B2 Peroxisome Proliferator-Activated Receptor (PPAR) activators such as 3-{4-[3-(4-benzyloxy-3-methoxyphenyl)propyl]-3-butoxyphenyl}propanoic acid, used in dermatology, cosmetics, cardiovascular diseases, immunology and/or lipid metabolism GALDERMA RESEARCH & DEVELOPMENT (FR) 2011-02-01 US disclosed
EP-2155662-B1 NOVEL DERIVATIVES OF 3-PHENYL PROPANOIC ACID ACTIVATING PPAR-TYPE RECEPTORS, METHOD FOR PREPARING SAME AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS GALDERMA RES & DEV (FR) 2010-12-01 EP disclosed
US-20100158843-A1 NOVEL 3-PHENYLPROPANOIC COMPOUND ACTIVATORS OF RECEPTORS OF PPAR TYPE AND PHARMACEUTICAL/COSMETIC COMPOSITIONS COMPRISED THEREOF GALDERMA RESEARCH & DEVELOPMENT (FR) 2010-06-24 US disclosed
EP-2155662-A2 NOVEL DERIVATIVES OF 3-PHENYL PROPANOIC ACID ACTIVATING PPAR-TYPE RECEPTORS, METHOD FOR PREPARING SAME AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS Galderma Research & Development (FR) 2010-02-24 EP disclosed
WO-2008152333-A9 NOVEL DERIVATIVES OF 3-PHENYL PROPANOIC ACID ACTIVATING PPAR-TYPE RECEPTORS, METHOD FOR PREPARING SAME AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS GALDERMA RESEARCH & DEVELOPMENT (FR) 2009-12-10 WO disclosed
WO-2008152333-A2 NOVEL DERIVATIVES OF 3-PHENYL PROPANOIC ACID ACTIVATING PPAR-TYPE RECEPTORS, METHOD FOR PREPARING SAME AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS GALDERMA RESEARCH & DEVELOPMENT (FR) 2008-12-18 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-20100158843-A1 NOVEL 3-PHENYLPROPANOIC COMPOUND ACTIVATORS OF RECEPTORS OF PPAR TYPE AND PHARMACEUTICAL/COSMETIC COMPOSITIONS COMPRISED THEREOF PPARG, PPARA, PPARD HDAC1 520/4885HDAC2 455/4885APP 1929/4885

“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.