SCHEMBL3227582

SCHEMBL3227582

Cc1ccc(CC(NC(=O)OCC2c3ccccc3-c3ccccc32)C(=O)O)cc1

nearest known ligand 0.63

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
MDM2 Q00987 3/20 0.58
MDM4 O15151 3/20 0.54
TP53 P04637 3/20 0.54
CASP3 P42574 2/20 0.52
PTPN1 P18031 1/20 0.47
TNF P01375 1/20 0.47
TLR2 O60603 2/20 0.47

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
SCHEMBL120602 1.00 MDM2 (0.58) MDM2MDM4TP53CASP3PTPN1
SCHEMBL30054917 1.00 MDM2 (0.58) MDM2MDM4TP53CASP3PTPN1
SCHEMBL29397837 1.00 MDM2 (0.58) MDM2MDM4TP53CASP3PTPN1
SCHEMBL29402291 1.00 MDM2 (0.58) MDM2MDM4TP53CASP3PTPN1
SCHEMBL118250 1.00 MDM2 (0.58) MDM2MDM4TP53CASP3PTPN1
SCHEMBL30051460 1.00 MDM2 (0.58) MDM2MDM4TP53CASP3PTPN1
SCHEMBL118169 0.92 MDM4 (0.59) MDM2MDM4TP53CASP3TNF
SCHEMBL29398498 0.92 MDM4 (0.59) MDM2MDM4TP53CASP3TNF
SCHEMBL119455 0.92 MDM4 (0.59) MDM2MDM4TP53CASP3TNF
SCHEMBL1228254 0.92 MDM4 (0.59) MDM2MDM4TP53CASP3TNF

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 23 patents — showing the first 20. 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-4339204-A1 BINDING MOLECULE EXHIBITING SELECTIVE BINDING FOR RAS(G12D) MUTANT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-03-20 EP disclosed
EP-4316503-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-02-07 EP disclosed
CN-117279928-A Process for the preparation of cyclic compounds comprising N-substituted amino acid residues 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
CN-117279655-A Pharmaceutical use of cyclic peptide compounds 中外制药株式会社 2023-12-22 CN disclosed
CN-117241817-A Formulations comprising cyclic peptide compounds and methods of making the same 中外制药株式会社 2023-12-15 CN disclosed
CN-114729006-A Cyclic peptide compounds having Kras inhibitory activity 中外制药株式会社 2022-07-08 CN disclosed
EP-3177611-B1 OPTIONALLY FUSED HETEROCYCLYL-SUBSTITUTED DERIVATIVES OF PYRIMIDINE USEFUL FOR THE TREATMENT OF INFLAMMATORY, METABOLIC, ONCOLOGIC AND AUTOIMMUNE DISEASES NUEVOLUTION AS (DK) 2021-10-06 EP disclosed
US-8338565-B2 Macrocyclic compounds for inhibition of tumor necrosis factor alpha ENSEMBLE THERAPEUTICS CORPORATION (US) 2012-12-25 US disclosed
US-8222210-B2 Methods of using substance P to promote healing of vascular wounds REID TED (US) 2012-07-17 US disclosed
US-7959990-B2 Adjustment of liquid crystals; oligomers, dendrimers, or polymer in solution is applied to support; crosslinking by radiation or polarized light ROLIC AG (CH) 2011-06-14 US disclosed
US-20100152099-A1 MACROCYCLIC COMPOUNDS FOR INHIBITION OF TUMOR NECROSIS FACTOR ALPHA ENSEMBLE THERAPEUTICS CORPORATION 2010-06-17 US disclosed
US-20100092561-A1 METHODS AND COMPOSITIONS USING SUBSTANCE P TO PROMOTE WOUND HEALING REID TED 2010-04-15 US disclosed
WO-2010022249-A2 MACROCYCLIC COMPOUNDS FOR INHIBITION OF TUMOR NECROSIS FACTOR ALPHA ENSEMBLE DISCOVERY CORPORATION (US) 2010-02-25 WO disclosed
US-20090005419-A1 Organic Compounds NOVARTIS AG (CH) 2009-01-01 US disclosed
US-20080274304-A1 Functionalized Photoreactive Compounds ROLIC AG (CH) 2008-11-06 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 (7 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-20080274304-A1 Functionalized Photoreactive Compounds PCNA, PIN1, MAP1LC3C MDM2 4042/4885MDM4 1486/4885TP53 4824/4885
US-20240400617-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION KRAS, NRAS, HRAS MDM2 164/4885MDM4 441/4885TP53 34/4885
US-20240239842-A1 BINDING MOLECULE EXHIBITING SELECTIVE BINDING FOR RAS(G12D) MUTANT KRAS, G3BP1, G3BP2 MDM2 47/4885MDM4 438/4885TP53 19/4885
US-20090005419-A1 Organic Compounds ELAVL1, RBM3, RRBP1 MDM2 639/4885MDM4 982/4885TP53 503/4885
US-20240148821-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND VIP, IAPP, KRAS MDM2 1604/4885MDM4 1294/4885TP53 178/4885
US-20100152099-A1 MACROCYCLIC COMPOUNDS FOR INHIBITION OF TUMOR NECROSIS FACTOR ALPHA TNF, CD40, TNFRSF1A MDM2 1236/4885MDM4 1060/4885TP53 573/4885
US-12371454-B2 Cyclic peptide compound having Kras inhibitory action KRAS, NRAS, HRAS MDM2 164/4885MDM4 441/4885TP53 34/4885

“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.