SCHEMBL3332061

SCHEMBL3332061

COCCOCOc1ccc(CCO)cc1Cl

nearest known ligand 0.44

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.44
GLA P06280 1/20 0.44
CSNK2A1 P68400 2/20 0.41
RARG P13631 2/20 0.38
PPARG P37231 1/20 0.38
HPGD P15428 2/20 0.37
NPC1 O15118 2/20 0.37
RAB9A P51151 2/20 0.37
BACE1 P56817 1/20 0.37
ATM Q13315 1/20 0.36
MAPT P10636 2/20 0.36
MAPK10 P53779 1/20 0.36
ALDH1A1 P00352 1/20 0.36
ACACB O00763 1/20 0.35

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
SCHEMBL3339746 0.84 KCNH2 (0.44) NPC1ATMMAPTALDH1A1
SCHEMBL3334100 0.83 RARG (0.37) RARGBACE1ATMMAPTALDH1A1
SCHEMBL3639108 0.81 PPARD (0.51) RARGPPARGALDH1A1
SCHEMBL3335702 0.79 ATM (0.46) SMN1; SMN2CSNK2A1RARGHPGDNPC1
SCHEMBL5759322 0.78 SMN1; SMN2 (0.47) SMN1; SMN2GLACSNK2A1PPARGHPGD
SCHEMBL3335173 0.77 LMNA (0.48) SMN1; SMN2ALDH1A1
SCHEMBL16954839 0.77 SMN1; SMN2 (0.52) SMN1; SMN2GLACSNK2A1HPGDNPC1
SCHEMBL7611761 0.77 MEN1 (0.53) SMN1; SMN2ATMMAPTALDH1A1
SCHEMBL5146702 0.77 SMN1; SMN2 (0.71) SMN1; SMN2GLACSNK2A1PPARGHPGD
SCHEMBL8767566 0.76 RARG (0.39) SMN1; SMN2RARGHPGDNPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8404836-B2 3-phenyl acrylic acid compound activators of type PPAR receptors and pharmaceutical/cosmetic compositions comprised thereof GALDERMA RESEARCH & DEVELOPMENT (FR) 2013-03-26 US disclosed
US-20100144884-A1 NOVEL 3-PHENYL ACRYLIC ACID COMPOUND ACTIVATORS OF TYPE PPAR RECEPTORS AND PHARMACEUTICAL/COSMETIC COMPOSITIONS COMPRISED THEREOF GALDERMA RESEARCH & DEVELOPMENT (FR) 2010-06-10 US disclosed
EP-2164827-A2 NOVEL DERIVATIVES OF 3-PHENYL ACRYLIC ACID ACTIVATING PPAR-TYPE RECEPTORS, METHOD FOR PREPARING SAME AND USE THEREOF IN COSMETIC OR PHARMACEUTICAL COMPOSITIONS Galderma Research & Development (FR) 2010-03-24 EP disclosed
WO-2008152334-A2 NOVEL DERIVATIVES OF 3-PHENYL ACRYLIC 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-20100144884-A1 NOVEL 3-PHENYL ACRYLIC ACID COMPOUND ACTIVATORS OF TYPE PPAR RECEPTORS AND PHARMACEUTICAL/COSMETIC COMPOSITIONS COMPRISED THEREOF PPARG, PPARA, PPARD SMN1; SMN2 4793/4885GLA 1585/4885CSNK2A1 4385/4885

“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.