SCHEMBL16574591

SCHEMBL16574591

CCOC(=O)[C@H](CS)NC(=O)C[C@H](NC(=O)OC(C)(C)C)C(=O)OCc1ccccc1

nearest known ligand 0.49

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
KLK5 Q9Y337 4/20 0.49
KLK7 P49862 2/20 0.49
TACR1 P25103 1/20 0.48
PPARA Q07869 3/20 0.48
SYK P43405 1/20 0.48
ACE P12821 1/20 0.47
CACNA1B Q00975 4/20 0.47
CTSS P25774 4/20 0.46
CTSK P43235 3/20 0.46
PPARG P37231 2/20 0.44
CTSL P07711 1/20 0.44
CTSB P07858 1/20 0.44

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
SCHEMBL23140704 1.00 KLK5 (0.49) KLK5KLK7TACR1PPARASYK
SCHEMBL23140735 0.90 ACE (0.51) KLK5KLK7TACR1PPARASYK
SCHEMBL15083163 0.90 ACE (0.51) KLK5KLK7TACR1PPARASYK
SCHEMBL6263802 0.89 PPARA (0.58) KLK5KLK7TACR1PPARASYK
SCHEMBL8316215 0.89 PPARA (0.58) KLK5KLK7TACR1PPARASYK
SCHEMBL12873045 0.89 PPARA (0.58) KLK5KLK7TACR1PPARASYK
SCHEMBL23056382 0.88 ACE (0.49) KLK5KLK7TACR1PPARASYK
SCHEMBL25491606 0.85 KLK7 (0.59) KLK5KLK7TACR1PPARASYK
SCHEMBL5419241 0.85 KLK7 (0.59) KLK5KLK7TACR1PPARASYK
SCHEMBL25715928 0.84 PPARA (0.56) KLK5KLK7TACR1PPARASYK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12415835-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-09-16 US disclosed
US-11891457-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-02-06 US disclosed
EP-3974563-A1 CYCLIC PEPTIDES Chugai Seiyaku Kabushiki Kaisha (JP) 2022-03-30 EP disclosed
EP-2813512-B1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI PHARMACEUTICAL CO LTD (JP) 2021-03-31 EP disclosed
US-20210061860-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2021-03-04 US disclosed
US-20160311858-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2016-10-27 US disclosed
US-9409952-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2016-08-09 US disclosed
US-9409952-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2016-08-09 US disclosed
US-20150080549-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2015-03-19 US disclosed
US-20150080549-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2015-03-19 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 (5 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 KLK5 403/4885KLK7 326/4885TACR1 172/4885
US-20210061860-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD VIP, NGLY1, GLP1R KLK5 403/4885KLK7 326/4885TACR1 172/4885
US-20160311858-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD VIP, NGLY1, GLP1R KLK5 403/4885KLK7 326/4885TACR1 172/4885
US-20150080549-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD VIP, NGLY1, GLP1R KLK5 403/4885KLK7 326/4885TACR1 172/4885
US-12415835-B2 Peptide-compound cyclization method VIP, NGLY1, GLP1R KLK5 403/4885KLK7 326/4885TACR1 172/4885

“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.