SCHEMBL29540316

SCHEMBL29540316

CCN(C(=O)OCC1c2ccccc2-c2ccccc21)[C@@H](Cc1ccccc1)C(=O)O

nearest known ligand 0.47

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
PPARG P37231 1/20 0.43
PPARA Q07869 1/20 0.43
ALDH1A1 P00352 1/20 0.42
LMNA P02545 1/20 0.42
POLB P06746 1/20 0.42
HSD17B10 Q99714 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
FABP5 Q01469 3/20 0.42
FABP7 O15540 2/20 0.42
KMT2A Q03164 2/20 0.40
CASP3 P42574 1/20 0.39
BCHE P06276 1/20 0.38
ACHE P22303 1/20 0.38
EPHX2 P34913 1/20 0.38
MDM4 O15151 1/20 0.37
TP53 P04637 1/20 0.37

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
SCHEMBL30744235 1.00 PPARG (0.43) PPARGPPARAALDH1A1LMNAPOLB
SCHEMBL16288980 1.00 PPARG (0.43) PPARGPPARAALDH1A1LMNAPOLB
SCHEMBL15083099 1.00 PPARG (0.43) PPARGPPARAALDH1A1LMNAPOLB
SCHEMBL31072747 0.93 PPARG (0.42) PPARGPPARAALDH1A1LMNAPOLB
SCHEMBL29855013 0.93 PPARG (0.42) PPARGPPARAALDH1A1LMNAPOLB
SCHEMBL25179041 0.93 PPARG (0.42) PPARGPPARAALDH1A1LMNAPOLB
SCHEMBL22454757 0.93 PPARG (0.42) PPARGPPARAALDH1A1LMNAPOLB
SCHEMBL25179288 0.92 PPARG (0.41) PPARGPPARAALDH1A1LMNAFABP5
SCHEMBL25185711 0.92 PPARG (0.41) PPARGPPARAALDH1A1LMNAFABP5
SCHEMBL29855192 0.92 PPARG (0.41) PPARGPPARAALDH1A1LMNAFABP5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250302912-A1 COMPOSITION INCLUDING PEPTIDE COMPOUND AND SURFACTANT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-10-02 US disclosed
US-12415835-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-09-16 US disclosed
US-12410212-B2 Cyclic compound having selective KRAS inhibitory effect on HRAS and NRAS CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-09-09 US disclosed
US-20250257094-A1 METHODS FOR PRODUCING CYCLIC COMPOUNDS COMPRISING N-SUBSTITUTED AMINO ACID RESIDUES CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-08-14 US disclosed
US-20250186542-A1 COMPOSITION CONTAINING PEPTIDE COMPOUND FOR USE WITH SURFACTANT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-06-12 US disclosed
US-12312379-B2 Methods for producing cyclic compounds comprising N-substituted amino acid residues CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-05-27 US disclosed
US-20240366711-A1 PREPARATION CONTAINING CYCLIC PEPTIDE COMPOUND AND METHOD FOR PRODUCING SAME CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-11-07 US disclosed
EP-4316503-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-02-07 EP disclosed
US-11891457-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-02-06 US disclosed
EP-4299069-A1 PREPARATION CONTAINING CYCLIC PEPTIDE COMPOUND AND METHOD FOR PRODUCING SAME CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-01-03 EP disclosed
CN-117279655-A Pharmaceutical use of cyclic peptide compounds 中外制药株式会社 2023-12-22 CN disclosed
CN-117279928-A Process for the preparation of cyclic compounds comprising N-substituted amino acid residues 中外制药株式会社 2023-12-22 CN disclosed
CN-117241817-A Formulations comprising cyclic peptide compounds and methods of making the same 中外制药株式会社 2023-12-15 CN disclosed
US-20220411462-A1 METHODS FOR PRODUCING CYCLIC COMPOUNDS COMPRISING N-SUBSTITUTED AMINO ACID RESIDUES CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2022-12-29 US disclosed
EP-4086272-A1 METHODS FOR PRODUCING CYCLIC COMPOUNDS COMPRISING N-SUBSTITUTED AMINO ACID RESIDUES Chugai Seiyaku Kabushiki Kaisha (JP) 2022-11-09 EP disclosed
EP-3974563-A1 CYCLIC PEPTIDES Chugai Seiyaku Kabushiki Kaisha (JP) 2022-03-30 EP 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 (9 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-11891457-B2 Peptide-compound cyclization method VIP, NGLY1, GLP1R PPARG 3973/4885PPARA 3215/4885ALDH1A1 4857/4885
US-20240366711-A1 PREPARATION CONTAINING CYCLIC PEPTIDE COMPOUND AND METHOD FOR PRODUCING SAME VIP, NGLY1, NPPA PPARG 3393/4885PPARA 2033/4885ALDH1A1 4841/4885
US-12410212-B2 Cyclic compound having selective KRAS inhibitory effect on HRAS and NRAS KRAS, HRAS, NRAS PPARG 2549/4885PPARA 2736/4885ALDH1A1 4331/4885
US-20220411462-A1 METHODS FOR PRODUCING CYCLIC COMPOUNDS COMPRISING N-SUBSTITUTED AMINO ACID RESIDUES NGLY1, NPPA, VIP PPARG 4325/4885PPARA 3049/4885ALDH1A1 4672/4885
US-20250186542-A1 COMPOSITION CONTAINING PEPTIDE COMPOUND FOR USE WITH SURFACTANT PCTP, CETP, PLTP PPARG 665/4885PPARA 471/4885ALDH1A1 4712/4885
US-12312379-B2 Methods for producing cyclic compounds comprising N-substituted amino acid residues NGLY1, NPPA, VIP PPARG 4325/4885PPARA 3049/4885ALDH1A1 4672/4885
US-20250257094-A1 METHODS FOR PRODUCING CYCLIC COMPOUNDS COMPRISING N-SUBSTITUTED AMINO ACID RESIDUES NGLY1, NPPA, VIP PPARG 4325/4885PPARA 3049/4885ALDH1A1 4672/4885
US-20250302912-A1 COMPOSITION INCLUDING PEPTIDE COMPOUND AND SURFACTANT PCTP, CETP, PLTP PPARG 874/4885PPARA 216/4885ALDH1A1 4623/4885
US-12415835-B2 Peptide-compound cyclization method VIP, NGLY1, GLP1R PPARG 3973/4885PPARA 3215/4885ALDH1A1 4857/4885

“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.