SCHEMBL30686153

SCHEMBL30686153

O=C(N[C@@H](Cc1ccc(C(F)(F)F)cc1)C(=O)O)OCC1c2ccccc2-c2ccccc21

nearest known ligand 0.59

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
MDM2 Q00987 4/20 0.59
FPR2 P25090 1/20 0.55
PTPN1 P18031 2/20 0.52
MDM4 O15151 3/20 0.52
TP53 P04637 3/20 0.52
CASP3 P42574 2/20 0.47
ITGB1 P05556 1/20 0.45
ITGA4 P13612 1/20 0.45
ITGB7 P26010 1/20 0.45

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
SCHEMBL2304920 1.00 MDM2 (0.59) MDM2FPR2PTPN1MDM4TP53
SCHEMBL29397862 1.00 MDM2 (0.59) MDM2FPR2PTPN1MDM4TP53
SCHEMBL2304915 1.00 MDM2 (0.59) MDM2FPR2PTPN1MDM4TP53
SCHEMBL29445591 1.00 MDM2 (0.59) MDM2FPR2PTPN1MDM4TP53
SCHEMBL3724885 1.00 MDM2 (0.59) MDM2FPR2PTPN1MDM4TP53
SCHEMBL8266129 0.91 PTPN1 (0.60) MDM2PTPN1
SCHEMBL8443984 0.90 MDM2 (0.51) MDM2FPR2PTPN1MDM4TP53
SCHEMBL8933064 0.90 MDM2 (0.52) MDM2FPR2PTPN1MDM4TP53
SCHEMBL25264909 0.90 MDM2 (0.62) MDM2PTPN1MDM4TP53CASP3
SCHEMBL30510289 0.90 MDM2 (0.62) MDM2PTPN1MDM4TP53CASP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4678652-A1 METHOD FOR PRODUCING CYCLIC PEPTIDE COMPOUND CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2026-01-14 EP 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
CN-120202211-A Cyclic compounds having selective KRAS inhibition over HRAS and NRAS 中外制药株式会社 2025-06-24 CN disclosed
WO-2025128624-A2 HYBRID PEPTIDE COMPOUNDS HAVING A SUBSTITUTED TRYPTOPHAN RESIDUE OR A TERMINAL SUBSTITUENT CARMOT THERAPEUTICS, INC. (US) 2025-06-19 WO disclosed
CN-119731195-A Cyclic compounds having selective inhibition of KRAS over HRAS and NRAS 中外制药株式会社 2025-03-28 CN disclosed
WO-2024219480-A1 METHOD FOR PRODUCING CYCLIC PEPTIDE COMPOUND 中外製薬株式会社 2024-10-24 WO disclosed
CN-117279655-A Pharmaceutical use of cyclic peptide compounds 中外制药株式会社 2023-12-22 CN disclosed
CN-117279933-A Cyclic compounds having selective KRAS inhibition relative to HRAS and NRAS 中外制药株式会社 2023-12-22 CN 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 (1 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-12410212-B2 Cyclic compound having selective KRAS inhibitory effect on HRAS and NRAS KRAS, HRAS, NRAS MDM2 30/4885FPR2 3678/4885PTPN1 1073/4885

“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.