Seladelpar

Seladelpar

SCHEMBL394392

CCOC(COc1ccc(C(F)(F)F)cc1)CSc1ccc(OCC(=O)O)c(C)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PPARD

The experimentally established mechanism targets of Seladelpar. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 2)

geneUniProtsupporting neighboursconfidence
PPARD known ✓ Q03181 20/20 1.00
PPARA Q07869 1/20 1.00

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
Seladelpar SCHEMBL392331 1.00 PPARD (1.00) PPARDPPARA
Seladelpar SCHEMBL390098 1.00 PPARD (1.00) PPARDPPARA
Seladelpar SCHEMBL29373526 1.00 PPARD (1.00) PPARDPPARA
SCHEMBL3701620 0.94 PPARD (1.00) PPARDPPARA
SCHEMBL16726808 0.94 PPARD (0.88) PPARDPPARA
SCHEMBL3695586 0.93 PPARD (1.00) PPARDPPARA
SCHEMBL377933 0.93 PPARD (1.00) PPARDPPARA
SCHEMBL377934 0.93 PPARD (1.00) PPARDPPARA
SCHEMBL3700528 0.93 PPARD (1.00) PPARDPPARA
SCHEMBL3694382 0.92 PPARD (1.00) PPARDPPARA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220370467-A1 USING OF A PPAR-DELTA AGONIST IN THE TREATMENT OF KIDNEY DISEASE WASHINGTON UNIVERSITY 2022-11-24 US claimed
US-11406611-B2 Treatment of intrahepatic cholestatic diseases CYMABAY THERAPEUTICS, INC. (US) 2022-08-09 US claimed
US-20220023306-A1 USE OF A PPAR-DELTA AGONIST IN THE TREATMENT OF FATTY ACID OXIDATION DISORDERS (FAOD) RENEO PHARMACEUTICALS, INC. 2022-01-27 US claimed
EP-3927718-A1 USE OF PPAR-DELTA AGONISTS IN THE TREATMENT OF MITOCHONDRIAL MYOPATHY Reneo Pharmaceuticals, Inc. (US) 2021-12-29 EP claimed
EP-3920903-A1 USE OF A PPAR-DELTA AGONIST IN THE TREATMENT OF FATTY ACID OXIDATION DISORDERS (FAOD) Reneo Pharmaceuticals, Inc. (US) 2021-12-15 EP claimed
CN-113747891-A Use of PPAR delta agonists in the treatment of Fatty Acid Oxidation Disorders (FAOD) 雷内奥制药公司 2021-12-03 CN claimed
CN-113710683-A Use of PPAR-delta agonists in the treatment of mitochondrial myopathy 雷内奥制药公司 2021-11-26 CN claimed
WO-2021055725-A1 USE OF A PPAR-DELTA AGONIST IN THE TREATMENT OF KIDNEY DISEASE RENEO PHARMACEUTICALS, INC. (US) 2021-03-25 WO claimed
US-20210023031-A1 Treatment of intrahepatic cholestatic diseases CYMABAY THERAPEUTICS, INC. (US) 2021-01-28 US claimed
US-10828273-B2 Treatment of intrahepatic cholestatic diseases CYMABAY THERAPEUTICS, INC. (US) 2020-11-10 US claimed
EP-1937065-B1 NOVEL LYSINE SALTS OF 4-((PHENOXYALKYL) THIO)-PHENOXYACETIC ACID DERIVATIVES JANSSEN PHARMACEUTICA NV (BE) 2015-01-28 EP claimed
US-8669288-B2 Lysine salts of 4-((phenoxyalkyl)thio)-phenoxyacetic acid derivatives JANSSEN PHARMACEUTICA N.V. (BE) 2014-03-11 US claimed
US-20130331453-A1 4-(PHENOXYALKYL)THIO)-PHENOXYACETIC ACIDS AND ANALOGS JANSSEN PHARMACEUTICA NV (BE) 2013-12-12 US claimed
EP-2100877-B1 4-((Phenoxyalkyl)thio)-phenoxyacetic acids and analogs JANSSEN PHARMACEUTICA NV (BE) 2012-01-25 EP claimed
US-20110105616-A1 NOVEL LYSINE SALTS OF 4-((PHENOXYALKYL)THIO)-PHENOXYACETIC ACID DERIVATIVES CYMABAY THERAPEUTICS, INC. 2011-05-05 US claimed
US-7709682-B2 Lysine salts of 4-((phenoxyalkyl)thio)-phenoxyacetic acid derivatives JANSSEN PHARMACEUTICA N.V. (BE) 2010-05-04 US claimed
EP-1937065-A2 NOVEL LYSINE SALTS OF 4-((PHENOXYALKYL) THIO)-PHENOXYACETIC ACID DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 2008-07-02 EP claimed
US-7301050-B2 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs JANSSEN PHARMACEUTICAL N.V. (BE) 2007-11-27 US claimed
WO-2007033231-A2 NOVEL LYSINE SALTS OF 4-((PHENOXYALKYL) THIO)-PHENOXYACETIC ACID DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 2007-03-22 WO claimed
US-20070060649-A1 NOVEL LYSINE SALTS OF 4-((PHENOXYALKYL)THIO)-PHENOXYACETIC ACID DERIVATIVES CYMABAY THERAPEUTICS, INC. 2007-03-15 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (8 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-20210023031-A1 Treatment of intrahepatic cholestatic diseases SLC10A1, SLC10A2, NR1H4 PPARD 1511/4885PPARA 1726/4885
US-11406611-B2 Treatment of intrahepatic cholestatic diseases SLC10A1, SLC10A2, NR1H4 PPARD 1511/4885PPARA 1726/4885
US-20220370467-A1 USING OF A PPAR-DELTA AGONIST IN THE TREATMENT OF KIDNEY DISEASE PPARG, PPARA, PPARD PPARD 3/4885PPARA 2/4885
US-20070060649-A1 NOVEL LYSINE SALTS OF 4-((PHENOXYALKYL)THIO)-PHENOXYACETIC ACID DERIVATIVES PPARA, PPARD, PPARG PPARD 2/4885PPARA 1/4885
US-20110105616-A1 NOVEL LYSINE SALTS OF 4-((PHENOXYALKYL)THIO)-PHENOXYACETIC ACID DERIVATIVES PPARA, PPARD, PPARG PPARD 2/4885PPARA 1/4885
US-20130331453-A1 4-(PHENOXYALKYL)THIO)-PHENOXYACETIC ACIDS AND ANALOGS PPARA, PPARG, PPARD PPARD 3/4885PPARA 1/4885
US-10828273-B2 Treatment of intrahepatic cholestatic diseases SLC10A1, SLC10A2, NR1H4 PPARD 1511/4885PPARA 1726/4885
US-20220023306-A1 USE OF A PPAR-DELTA AGONIST IN THE TREATMENT OF FATTY ACID OXIDATION DISORDERS (FAOD) PPARD, ACOX1, CPT1A PPARD 1/4885PPARA 8/4885

“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.