SCHEMBL2450141

SCHEMBL2450141

O=C(Cl)C(Oc1cccc(C(F)(F)F)c1)c1ccc(Cl)cc1

nearest known ligand 0.81

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
PPARG P37231 8/20 0.81
SLC22A12 Q96S37 1/20 0.62
PPARA Q07869 3/20 0.46
P2RY1 P47900 1/20 0.43
KDM4E B2RXH2 1/20 0.42
LMNA P02545 1/20 0.41
MAPT P10636 1/20 0.41
HTT P42858 1/20 0.41
CNR2 P34972 1/20 0.40
ALDH1A1 P00352 1/20 0.40
HPGD P15428 1/20 0.40
PTGER4 P35408 1/20 0.40
RHOC P08134 1/20 0.40
RHOA P61586 1/20 0.40
MRGPRX4 Q96LA9 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
SCHEMBL12189841 1.00 PPARG (0.81) PPARGSLC22A12PPARAP2RY1KDM4E
Metaglidasen SCHEMBL29387584 0.89 PPARG (1.00) PPARGSLC22A12PPARAP2RY1KDM4E
Metaglidasen SCHEMBL14606136 0.89 PPARG (1.00) PPARGSLC22A12PPARAP2RY1KDM4E
Metaglidasen SCHEMBL2443233 0.89 PPARG (1.00) PPARGSLC22A12PPARAP2RY1KDM4E
Mbx-102 Acid Form SCHEMBL12189837 0.89 PPARG (1.00) PPARGSLC22A12PPARAP2RY1KDM4E
SCHEMBL15267524 0.88 PPARG (0.79) PPARGSLC22A12PPARAP2RY1KDM4E
SCHEMBL18174524 0.88 PPARG (0.79) PPARGSLC22A12PPARAP2RY1KDM4E
SCHEMBL11741264 0.88 PPARG (0.79) PPARGSLC22A12PPARAP2RY1KDM4E
SCHEMBL18174520 0.88 PPARG (0.79) PPARGSLC22A12PPARAP2RY1KDM4E
Metaglidasen SCHEMBL11733289 0.88 PPARG (0.97) PPARGSLC22A12PPARAP2RY1KDM4E

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 61 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160075636-A1 Process for the Preparation of (-)-(4-Chloro-Phenyl)-(3-Trifluoromethyl-Phenoxy)-Acetic Acid 2-Acetylamino-Ethyl Ester CYMABAY THERAPEUTICS, INC. (US) 2016-03-17 US disclosed
US-8541614-B2 Process for the preparation of (−)-(4-chloro-phenyl)-(3-trifluoromethyl-phenoxy)-acetic acid 2-acetylamino-ethyl ester METABOLEX, INC. (US) 2013-09-24 US disclosed
US-8481597-B2 Use of (-) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of insulin resistance, type 2 diabetes, hyperlipidemia and hyperuricemia METABOLEX, INC. (US) 2013-07-09 US disclosed
US-8481597-B2 Use of (-) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of insulin resistance, type 2 diabetes, hyperlipidemia and hyperuricemia METABOLEX, INC. (US) 2013-07-09 US disclosed
US-8481597-B2 Use of (-) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of insulin resistance, type 2 diabetes, hyperlipidemia and hyperuricemia METABOLEX, INC. (US) 2013-07-09 US disclosed
US-8354448-B2 Use of (−)(3-trihalomethylphenoxy)(4-halophenyl) acetic acid derivatives for treatment of type 2 diabetes METABOLEX, INC. (US) 2013-01-15 US disclosed
US-8354448-B2 Use of (−)(3-trihalomethylphenoxy)(4-halophenyl) acetic acid derivatives for treatment of type 2 diabetes METABOLEX, INC. (US) 2013-01-15 US disclosed
US-8354448-B2 Use of (−)(3-trihalomethylphenoxy)(4-halophenyl) acetic acid derivatives for treatment of type 2 diabetes METABOLEX, INC. (US) 2013-01-15 US disclosed
US-8329749-B2 Use of (−) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of hyperuricemia METABOLEX, INC. (US) 2012-12-11 US disclosed
US-8329749-B2 Use of (−) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of hyperuricemia METABOLEX, INC. (US) 2012-12-11 US disclosed
US-6624194-B1 3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives and compositions in the treatment of insulin resistance, Type 2 diabetes, hyperlipidemia and hyperuricemia. Provides (3-trihalomethylphenoxy) (4-halophenyl) acetic acid for METABOLEX, INC. 2003-09-23 US disclosed
EP-1343493-A2 USE OF(-) (3-HALOMETHYLPHENOXY) (4-HALOPHENYL) ACETIC ACID DERIVATIVES FOR TREATMENT OF INSULIN RESISTANCE, TYPE 2 DIABETES, HYPERLIPIDEMIA AND HYPERURICEMIA METABOLEX, INC. (US) 2003-09-17 EP disclosed
US-6613802-B1 Composition containing (-) enantiomer of compound in enantiomeric excess of at least 80% relative to (+) enantiomer, which exhibits reduced inhibition of cytochrome P450 2C9 METABOLEX, INC. 2003-09-02 US disclosed
WO-2002044113-A9 USE OF(-) (3-HALOMETHYLPHENOXY) (4-HALOPHENYL) ACETIC ACID DERIVATIVES FOR TREATMENT OF INSULIN RESISTANCE, TYPE 2 DIABETES, HYPERLIPIDEMIA AND HYPERURICEMIA METABOLEX INC (US) 2003-05-01 WO disclosed
WO-2002044113-A2 USE OF(-) (3-HALOMETHYLPHENOXY) (4-HALOPHENYL) ACETIC ACID DERIVATIVES FOR TREATMENT OF INSULIN RESISTANCE, TYPE 2 DIABETES, HYPERLIPIDEMIA AND HYPERURICEMIA METABOLEX, INC. (US) 2002-06-06 WO disclosed
EP-1183020-A2 USE OF(-)(3-TRIHALOMETHYLPHENOXY) (4-HALOPHENYL)ACETIC ACID DERIVATIVES FOR TREATMENT OF INSULIN RESISTANCE, TYPE 2 DIABETES, HYPERLIPIDAEMIA AND HYPERURICAEMIA METABOLEX, INC. (US) 2002-03-06 EP disclosed
US-6262118-B1 THERAPY OF TYPE 2 DIABETES IN A MAMMAL BY ADMINISTERING (-) 4-CHLOROPHENYL-(3-TRIFLUOROMETHYLPHENOXY)ACETIC ACID DERIVATIVE METABOLEX, INC. 2001-07-17 US disclosed
WO-2000074666-A2 USE OF (-) (3-TRIHALOMETHYLPHENOXY) (4-HALOPHENYL) ACETIC ACID DERIVATIVES FOR TREATMENT OF INSULIN RESISTANCE, TYPE 2 DIABETES, HYPERLIPIDAEMIA AND HYPERURICAEMIA METABOLEX, INC. (US) 2000-12-14 WO disclosed
US-4055653-A Sulfur containing trialkoxybenzoylamino carboxylic acids DEUTSCHE GOLD- UND SILBER-SCHEIDEANSTALT VORMALS ROESSLER (DT) 1977-10-25 US disclosed
US-4055592-A ATHEROSCLEROSIS MERCK & CO., INC. (US) 1977-10-25 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-20160075636-A1 Process for the Preparation of (-)-(4-Chloro-Phenyl)-(3-Trifluoromethyl-Phenoxy)-Acetic Acid 2-Acetylamino-Ethyl Ester PC, ACACA, ACACB PPARG 136/4885SLC22A12 2169/4885PPARA 140/4885

“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.