SCHEMBL29670345

SCHEMBL29670345

O=C(O)CN(Cc1ccccc1)C(=O)OCC1c2ccccc2-c2ccccc21

nearest known ligand 0.45

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.45
FABP5 Q01469 3/20 0.45
FABP7 O15540 2/20 0.45
EPHX2 P34913 1/20 0.41
OPRD1 P41143 1/20 0.40
CASP3 P42574 2/20 0.39
CA1 P00915 1/20 0.38
CA2 P00918 1/20 0.38
MEN1 O00255 1/20 0.38

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
SCHEMBL800081 1.00 KMT2A (0.45) KMT2AFABP5FABP7EPHX2OPRD1
SCHEMBL31437116 1.00 KMT2A (0.45) KMT2AFABP5FABP7EPHX2OPRD1
SCHEMBL22960719 0.92 KMT2A (0.41) KMT2AFABP5FABP7EPHX2CASP3
SCHEMBL1869833 0.90 FABP5 (0.50) KMT2AFABP5FABP7EPHX2OPRD1
SCHEMBL30639568 0.87 KMT2A (0.44) KMT2AFABP5FABP7EPHX2OPRD1
SCHEMBL21952273 0.87 KMT2A (0.44) KMT2AFABP5FABP7EPHX2OPRD1
SCHEMBL31370279 0.87 PPARG (0.45) FABP5
SCHEMBL21950699 0.85 KMT2A (0.46) KMT2AFABP5FABP7EPHX2CASP3
SCHEMBL31278102 0.85 KMT2A (0.46) KMT2AFABP5FABP7EPHX2CASP3
SCHEMBL831614 0.84 KMT2A (0.45) KMT2AFABP5FABP7EPHX2CASP3

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 7 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-12240871-B2 Method for producing peptide compound NISSAN CHEMICAL CORPORATION (JP) 2025-03-04 US disclosed
US-20240400617-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-12-05 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
US-20220153777-A1 METHOD FOR PRODUCING PEPTIDE COMPOUND NISSAN CHEMICAL CORPORATION (JP) 2022-05-19 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 (6 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 KMT2A 3145/4885FABP5 4094/4885FABP7 4602/4885
US-20240400617-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION KRAS, NRAS, HRAS KMT2A 3145/4885FABP5 4094/4885FABP7 4602/4885
US-20240148821-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND VIP, IAPP, KRAS KMT2A 4757/4885FABP5 4026/4885FABP7 4376/4885
US-12240871-B2 Method for producing peptide compound NGLY1, NPPA, NPEPPS KMT2A 3924/4885FABP5 1733/4885FABP7 576/4885
US-20220153777-A1 METHOD FOR PRODUCING PEPTIDE COMPOUND NGLY1, NPPA, NPEPPS KMT2A 3924/4885FABP5 1733/4885FABP7 576/4885
US-12371454-B2 Cyclic peptide compound having Kras inhibitory action KRAS, NRAS, HRAS KMT2A 3145/4885FABP5 4094/4885FABP7 4602/4885

“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.