SCHEMBL22388724

SCHEMBL22388724

O=C(C[C@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)N1CCCCC1)OC(c1ccccc1)(c1ccc(C2CCCCCCCCCCC2)cc1)c1ccccc1Cl

nearest known ligand 0.38

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
▸ MDM4 O15151 2/20 0.38
▸ TP53 P04637 2/20 0.38
▸ CCR1 P32246 7/20 0.36
▸ MDM2 Q00987 1/20 0.35
▸ CASP3 P42574 2/20 0.34
▸ BACE1 P56817 1/20 0.34
▸ CALCRL Q16602 1/20 0.33

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
SCHEMBL21950768 1.00 MDM4 (0.38) MDM4TP53CCR1MDM2CASP3
SCHEMBL22388723 1.00 MDM4 (0.38) MDM4TP53CCR1MDM2CASP3
SCHEMBL21950769 1.00 MDM4 (0.38) MDM4TP53CCR1MDM2CASP3
SCHEMBL24414066 1.00 MDM4 (0.38) MDM4TP53CCR1MDM2CASP3
SCHEMBL24965903 1.00 MDM4 (0.38) MDM4TP53CCR1MDM2CASP3
SCHEMBL24965995 1.00 MDM4 (0.38) MDM4TP53CCR1MDM2CASP3
SCHEMBL24828833 1.00 MDM4 (0.38) MDM4TP53CCR1MDM2CASP3
SCHEMBL24414034 1.00 MDM4 (0.38) MDM4TP53CCR1MDM2CASP3
SCHEMBL21895947 1.00 MDM4 (0.38) MDM4TP53CCR1MDM2CASP3
SCHEMBL25658437 1.00 MDM4 (0.38) MDM4TP53CCR1MDM2CASP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11787836-B2 Method for synthesizing peptide containing N-substituted amino acid CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-10-17 — — US disclosed
US-20230151060-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-05-18 — — US disclosed
US-20230138226-A1 METHOD FOR SYNTHESIZING PEPTIDE CONTAINING N-SUBSTITUTED AMINO ACID CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-05-04 — — US disclosed
US-11542299-B2 Method for synthesizing peptide containing N-substituted amino acid CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-01-03 — — US disclosed
US-20200277327-A1 METHOD FOR SYNTHESIZING PEPTIDE CONTAINING N-SUBSTITUTED AMINO ACID CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2020-09-03 — — 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 MDM4 441/4885TP53 34/4885CCR1 1767/4885
US-20200277327-A1 METHOD FOR SYNTHESIZING PEPTIDE CONTAINING N-SUBSTITUTED AMINO ACID NPPA, VIP, DNPEP MDM4 4142/4885TP53 2781/4885CCR1 3629/4885
US-20230138226-A1 METHOD FOR SYNTHESIZING PEPTIDE CONTAINING N-SUBSTITUTED AMINO ACID NPPA, VIP, DNPEP MDM4 4142/4885TP53 2781/4885CCR1 3629/4885
US-11542299-B2 Method for synthesizing peptide containing N-substituted amino acid NPPA, VIP, DNPEP MDM4 4142/4885TP53 2781/4885CCR1 3629/4885
US-11787836-B2 Method for synthesizing peptide containing N-substituted amino acid NPPA, VIP, DNPEP MDM4 4142/4885TP53 2781/4885CCR1 3629/4885

“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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