SCHEMBL25185739

SCHEMBL25185739

COC(=O)N(C1c2ccccc2-c2ccccc21)[C@@H](Cc1cccc(I)c1)C(=O)O

nearest known ligand 0.37

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ CTSB P07858 1/20 0.37
▸ SLC7A5 Q01650 2/20 0.35
▸ ALB P02768 1/20 0.34
▸ IL2 P60568 1/20 0.34
▸ MAPT P10636 1/20 0.33
▸ SIGMAR1 Q99720 1/20 0.33
▸ FOLH1 Q04609 1/20 0.33
▸ PTGER1 P34995 1/20 0.32
▸ PTGER4 P35408 1/20 0.32
▸ PTGER3 P43115 1/20 0.32
▸ PTGER2 P43116 1/20 0.32
▸ FPR2 P25090 3/20 0.32
▸ PPARG P37231 1/20 0.32
▸ PPARA Q07869 1/20 0.32
▸ CTRB1 P17538 1/20 0.32

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
SCHEMBL4600067 0.89 CTRB1 (0.40) MAPTPPARGPPARACTRB1
SCHEMBL30510366 0.89 CTRB1 (0.40) MAPTPPARGPPARACTRB1
SCHEMBL5407004 0.89 CTRB1 (0.40) MAPTPPARGPPARACTRB1
SCHEMBL4600752 0.89 CTRB1 (0.40) MAPTPPARGPPARACTRB1
SCHEMBL25182258 0.88 POLB (0.39) CTSBSLC7A5MAPTPPARGPPARA
SCHEMBL25179512 0.87 PTGES (0.40) CTSBSIGMAR1
SCHEMBL25182256 0.87 PLA2G1B (0.39) CTSB
SCHEMBL30510319 0.87 PLA2G1B (0.39) CTSB
SCHEMBL25186573 0.87 SLC1A1 (0.41) MAPTPPARGPPARA
SCHEMBL25183036 0.87 RAB9A (0.43) PPARA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12371454-B2 Cyclic peptide compound having Kras inhibitory action CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-07-29 — — US disclosed
US-20240400617-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-12-05 — — US disclosed
US-20240239842-A1 BINDING MOLECULE EXHIBITING SELECTIVE BINDING FOR RAS(G12D) MUTANT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-07-18 — — US disclosed
US-20240148821-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-05-09 — — US disclosed
EP-4316503-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-02-07 — — EP disclosed
US-20230151060-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-05-18 — — 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-20230151060-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION KRAS, NRAS, HRAS CTSB 2004/4885SLC7A5 2107/4885ALB 3191/4885
US-20240400617-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION KRAS, NRAS, HRAS CTSB 2004/4885SLC7A5 2107/4885ALB 3191/4885
US-20240239842-A1 BINDING MOLECULE EXHIBITING SELECTIVE BINDING FOR RAS(G12D) MUTANT KRAS, G3BP1, G3BP2 CTSB 3339/4885SLC7A5 4073/4885ALB 2817/4885
US-20240148821-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND VIP, IAPP, KRAS CTSB 504/4885SLC7A5 1197/4885ALB 2660/4885
US-12371454-B2 Cyclic peptide compound having Kras inhibitory action KRAS, NRAS, HRAS CTSB 2004/4885SLC7A5 2107/4885ALB 3191/4885

“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.

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