SCHEMBL4522014

SCHEMBL4522014

Cc1cc(Oc2ccc(CC(=O)O)cc2C)cc(Oc2ccc(Cl)cc2Oc2ccccc2)c1

nearest known ligand 0.50

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
FFAR1 O14842 4/20 0.50
FFAR4 Q5NUL3 3/20 0.50
SRD5A2 P31213 1/20 0.49
PTGDR2 Q9Y5Y4 3/20 0.46
L3MBTL1 Q9Y468 2/20 0.43
CARM1 Q86X55 2/20 0.43
PRMT6 Q96LA8 2/20 0.43
PPARG P37231 1/20 0.43
PPARD Q03181 1/20 0.43
PPARA Q07869 1/20 0.43
CHRM1 P11229 1/20 0.41
LMNA P02545 1/20 0.41
STK39 Q9UEW8 1/20 0.41
GAA P10253 1/20 0.40
PTGDR Q13258 1/20 0.40
NR3C1 P04150 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
SCHEMBL4516754 0.91 SRD5A2 (0.50) FFAR1FFAR4SRD5A2PTGDR2L3MBTL1
SCHEMBL4525574 0.89 PTGDR2 (0.56) FFAR1FFAR4SRD5A2PTGDR2L3MBTL1
SCHEMBL13678675 0.80 SRD5A2 (0.53) FFAR1FFAR4SRD5A2L3MBTL1PPARD
SCHEMBL5989516 0.79 PPARG (0.65) FFAR1FFAR4SRD5A2PTGDR2L3MBTL1
SCHEMBL5989519 0.79 PPARG (0.65) FFAR1FFAR4SRD5A2PTGDR2L3MBTL1
SCHEMBL4516303 0.78 FFAR1 (0.59) FFAR1FFAR4PTGDR2L3MBTL1PPARG
SCHEMBL4525120 0.77 PPARG (0.65) FFAR1FFAR4PPARGPPARDPPARA
SCHEMBL4518589 0.76 PPARG (0.44) FFAR1FFAR4L3MBTL1PPARGPPARD
SCHEMBL4522006 0.74 PPARD (0.65) FFAR1FFAR4PTGDR2L3MBTL1PPARG
SCHEMBL4528795 0.74 PPARG (0.64) FFAR1FFAR4PPARGPPARDPPARA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7608639-B2 Phenoxyether derivatives as PPAR modulators ELI LILLY AND COMPANY (US) 2009-10-27 US disclosed
US-7608639-B2 Phenoxyether derivatives as PPAR modulators ELI LILLY AND COMPANY (US) 2009-10-27 US disclosed
US-7608639-B2 Phenoxyether derivatives as PPAR modulators ELI LILLY AND COMPANY (US) 2009-10-27 US disclosed
US-20070037812-A1 Such as 3-{4-[3-(4-Chloro-2- phenoxy-phenoxy)- phenoxy]-2-methyl- phenyl}-propionic acid; peroxisome proliferator activated receptor (PPAR); syndrome X, type II diabetes, hyperglycemia, hyperlipidemia, obesity, coagaulopathy, hypertension, arteriosclerosis ELI LILLY AND COMPANY (US) 2007-02-15 US disclosed
US-20070037812-A1 Such as 3-{4-[3-(4-Chloro-2- phenoxy-phenoxy)- phenoxy]-2-methyl- phenyl}-propionic acid; peroxisome proliferator activated receptor (PPAR); syndrome X, type II diabetes, hyperglycemia, hyperlipidemia, obesity, coagaulopathy, hypertension, arteriosclerosis ELI LILLY AND COMPANY (US) 2007-02-15 US disclosed
US-20070037812-A1 Such as 3-{4-[3-(4-Chloro-2- phenoxy-phenoxy)- phenoxy]-2-methyl- phenyl}-propionic acid; peroxisome proliferator activated receptor (PPAR); syndrome X, type II diabetes, hyperglycemia, hyperlipidemia, obesity, coagaulopathy, hypertension, arteriosclerosis ELI LILLY AND COMPANY (US) 2007-02-15 US disclosed
EP-1675814-A1 PHENOXYETHER DERIVATIVES AS PPAR MODULATORS ELI LILLY AND COMPANY (US) 2006-07-05 EP disclosed
WO-2005037763-A1 PHENOXYETHER DERIVATIVES AS PPAR MODULATORS ELI LILLY AND COMPANY (US) 2005-04-28 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-20070037812-A1 Such as 3-{4-[3-(4-Chloro-2- phenoxy-phenoxy)- phenoxy]-2-methyl- phenyl}-propionic acid; peroxisome proliferator activated receptor (PPAR); syndrome X, type II diabetes, hyperglycemia, hyperlipidemia, obesity, coagaulopathy, hypertension, arteriosclerosis PPARA, PPARG, PPARD FFAR1 22/4885FFAR4 19/4885SRD5A2 164/4885

“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.