SCHEMBL1000833

SCHEMBL1000833

CC(C)(C)OC(=O)n1cc(CC(NC(=O)OCC2c3ccccc3-c3ccccc32)C(=O)O)c2ccccc21

nearest known ligand 0.77

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
▸ ADAM17 P78536 1/20 0.51
▸ MDM4 O15151 3/20 0.49
▸ TP53 P04637 3/20 0.49
▸ MDM2 Q00987 4/20 0.48
▸ L3MBTL1 Q9Y468 1/20 0.48
▸ SLC17A5 Q9NRA2 1/20 0.43
▸ CCKAR P32238 2/20 0.43
▸ CCKBR P32239 2/20 0.43
▸ OPRD1 P41143 2/20 0.43
▸ BACE1 P56817 1/20 0.43
▸ EPHX1 P07099 1/20 0.43

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
SCHEMBL30917941 1.00 ADAM17 (0.51) ADAM17MDM4TP53MDM2L3MBTL1
SCHEMBL5969202 1.00 ADAM17 (0.51) ADAM17MDM4TP53MDM2L3MBTL1
SCHEMBL29353403 1.00 ADAM17 (0.51) ADAM17MDM4TP53MDM2L3MBTL1
SCHEMBL29364320 1.00 ADAM17 (0.51) ADAM17MDM4TP53MDM2L3MBTL1
SCHEMBL1709188 1.00 ADAM17 (0.51) ADAM17MDM4TP53MDM2L3MBTL1
SCHEMBL12052757 0.93 L3MBTL1 (0.48) ADAM17MDM4TP53MDM2L3MBTL1
SCHEMBL8104292 0.93 L3MBTL1 (0.48) ADAM17MDM4TP53MDM2L3MBTL1
SCHEMBL30231797 0.93 ADAM17 (0.51) ADAM17MDM4TP53MDM2L3MBTL1
SCHEMBL119657 0.92 MDM4 (0.53) MDM4TP53MDM2SLC17A5
SCHEMBL120776 0.92 MDM4 (0.53) MDM4TP53MDM2SLC17A5

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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4698551-A1 NOVEL SMALL MOLECULE AGONISTS OF INSULIN RECEPTOR (INSR) AS ANTI-DIABETES DRUGS The University of Hong Kong (CN) 2026-02-25 — — EP disclosed
US-12415835-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-09-16 — — US disclosed
WO-2024217497-A1 NOVEL SMALL MOLECULE AGONISTS OF INSULIN RECEPTOR (INSR) AS ANTI-DIABETES DRUGS THE UNIVERSITY OF HONG KONG (CN) 2024-10-24 — — WO disclosed
US-20240166689-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-05-23 — — US disclosed
US-20240076311-A1 METHOD FOR SYNTHESIZING PEPTIDE THIOESTERS AND HEAD-TO-TAIL AMIDE CYCLIC PEPTIDE THEREOF JIANGSU GENSCRIPT BIOTECH CO., LTD. (CN) 2024-03-07 — — US disclosed
US-11891457-B2 Peptide-compound cyclization method CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-02-06 — — US disclosed
EP-3974563-A1 CYCLIC PEPTIDES Chugai Seiyaku Kabushiki Kaisha (JP) 2022-03-30 — — EP disclosed
EP-2813512-B1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI PHARMACEUTICAL CO LTD (JP) 2021-03-31 — — EP disclosed
US-20210061860-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2021-03-04 — — US disclosed
US-9738660-B2 Selective inhibitors for protein kinases and pharmaceutical composition and use thereof NATIONAL CHIAO TUNG UNIVERSITY (CN) 2017-08-22 — — US disclosed
US-20100144648-A1 COMPOUNDS FOR ENZYME INHIBITION ONYX THERAPEUTICS, INC. (US) 2010-06-10 — — US disclosed
US-7691852-B2 Compounds for enzyme inhibition ONYX THERAPEUTICS, INC. (US) 2010-04-06 — — US disclosed
EP-2147925-A1 Compositions of lipopeptide antibiotic derivatives and methods of use thereof MIGENIX INC. (CA) 2010-01-27 — — EP disclosed
EP-1791837-B1 SUBSTITUTED HYDANTOINS FOR THE TREATMENT OF CANCER HOFFMANN LA ROCHE (CH) 2009-08-19 — — EP disclosed
US-20090005419-A1 Organic Compounds NOVARTIS AG (CH) 2009-01-01 — — US disclosed
US-7371869-B2 Substituted hydantoins HOFFMANN-LA ROCHE INC. (US) 2008-05-13 — — US disclosed
EP-1656390-A2 COMPOSITIONS OF LIPOPEPTIDE ANTIBIOTIC DERIVATIVES AND METHODS OF USE THEREOF MIGENIX INC. (CA) 2006-05-17 — — EP disclosed
US-20060063814-A1 Substituted hydantoins GOODNOW ROBERT A JR 2006-03-23 — — US disclosed
US-20050153876-A1 Compositions of lipopeptide antibiotic derivatives and methods of use thereof MIGENIX INC. (CA) 2005-07-14 — — US disclosed
WO-2005000878-A2 COMPOSITIONS OF LIPOPEPTIDE ANTIBIOTIC DERIVATIVES AND METHODS OF USE THEREOF MIGENIX INC. (CA) 2005-01-06 — — WO 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 (9 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-11891457-B2 Peptide-compound cyclization method VIP, NGLY1, GLP1R ADAM17 15/4885MDM4 3559/4885TP53 2654/4885
US-20240076311-A1 METHOD FOR SYNTHESIZING PEPTIDE THIOESTERS AND HEAD-TO-TAIL AMIDE CYCLIC PEPTIDE THEREOF VIP, CETP, PITHD1 ADAM17 1120/4885MDM4 3923/4885TP53 954/4885
US-20210061860-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD VIP, NGLY1, GLP1R ADAM17 15/4885MDM4 3559/4885TP53 2654/4885
US-20240166689-A1 PEPTIDE-COMPOUND CYCLIZATION METHOD VIP, NGLY1, GLP1R ADAM17 15/4885MDM4 3559/4885TP53 2654/4885
US-20090005419-A1 Organic Compounds ELAVL1, RBM3, RRBP1 ADAM17 4511/4885MDM4 982/4885TP53 503/4885
US-20050153876-A1 Compositions of lipopeptide antibiotic derivatives and methods of use thereof NRDC, NOD2, NGLY1 ADAM17 141/4885MDM4 2087/4885TP53 2126/4885
US-20060063814-A1 Substituted hydantoins HNMT, MAPK6, KYNU ADAM17 2321/4885MDM4 3878/4885TP53 913/4885
US-20100144648-A1 COMPOUNDS FOR ENZYME INHIBITION PSME1, PSMB1, PSME3 ADAM17 464/4885MDM4 1727/4885TP53 331/4885
US-12415835-B2 Peptide-compound cyclization method VIP, NGLY1, GLP1R ADAM17 15/4885MDM4 3559/4885TP53 2654/4885

“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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