SCHEMBL178741

SCHEMBL178741

C=CCOC(=O)CCC(NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O

nearest known ligand 0.52

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
▸ MDM4 O15151 2/20 0.51
▸ TP53 P04637 2/20 0.51
▸ TLR2 O60603 2/20 0.51
▸ CASP3 P42574 2/20 0.48
▸ MDM2 Q00987 5/20 0.48
▸ CASP1 P29466 2/20 0.47
▸ TNF P01375 1/20 0.47
▸ SLC17A5 Q9NRA2 1/20 0.45
▸ KMT2A Q03164 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
SCHEMBL29407853 1.00 MDM4 (0.51) MDM4TP53TLR2CASP3MDM2
SCHEMBL29376536 1.00 MDM4 (0.51) MDM4TP53TLR2CASP3MDM2
SCHEMBL119481 1.00 MDM4 (0.51) MDM4TP53TLR2CASP3MDM2
SCHEMBL30055069 1.00 MDM4 (0.51) MDM4TP53TLR2CASP3MDM2
SCHEMBL25358998 0.94 MDM2 (0.51) MDM4TP53TLR2CASP3MDM2
SCHEMBL31398353 0.94 MDM2 (0.51) MDM4TP53TLR2CASP3MDM2
SCHEMBL31398346 0.94 MDM2 (0.51) MDM4TP53TLR2CASP3MDM2
SCHEMBL31689003 0.93 MDM2 (0.50) MDM4TP53TLR2CASP3MDM2
SCHEMBL29398655 0.92 TLR2 (0.48) MDM4TP53TLR2CASP3MDM2
SCHEMBL14417867 0.91 CASP3 (0.46) MDM4TP53TLR2CASP3MDM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4667483-A1 HUMAN TRANSFERRIN RECEPTOR-BINDING PEPTIDE JCR Pharmaceuticals Co., Ltd. (JP) 2025-12-24 — — EP disclosed
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
WO-2024172166-A1 HUMAN TRANSFERRIN RECEPTOR-BINDING PEPTIDE JCRファーマ株式会社 2024-08-22 — — WO 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
CN-117279655-A Pharmaceutical use of cyclic peptide compounds 中外制药株式会社 2023-12-22 — — CN disclosed
US-20230151060-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-05-18 — — US disclosed
EP-4043478-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITING ACTION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2022-08-17 — — EP disclosed
CN-114729006-A Cyclic peptide compounds having Kras inhibitory activity 中外制药株式会社 2022-07-08 — — CN disclosed
CN-112188902-A Modified self-immolative moieties for prodrugs and conjugates and methods of use and manufacture 百时美施贵宝公司 2021-01-05 — — CN disclosed
US-8895231-B2 Patterning process and resist composition SHIN-ETSU CHEMICAL CO., LTD. (JP) 2014-11-25 — — US disclosed
US-20120058428-A1 PATTERNING PROCESS AND RESIST COMPOSITION SHIN-ETSU CHEMICAL CO., LTD. (JP) 2012-03-08 — — US disclosed
US-6040323-A INHIBITING CELL PROLIFERATION OF HUMAN BREAST CANCER CELLS UNIVERSITY OF PITTSBURGH (US) 2000-03-21 — — US disclosed
EP-0959884-A4 — — 1999-12-15 — — EP disclosed
EP-0959884-A1 PHOSPHATASE INHIBITORS AND METHODS OF USE THEREOF UNIVERSITY OF PITTSBURGH (US) 1999-12-01 — — EP disclosed
US-5925660-A ENZYME INHIBITORS FOR PHOSPHATASE UNIVERSITY OF PITTSBURGH (US) 1999-07-20 — — US disclosed
US-5856506-A (OXAZOLYLCARBONYLAMINO)ETHYLAMINO GLUTAMATE DERIVATIVES UNIVERSITY OF PITTSBURGH (US) 1999-01-05 — — US disclosed
WO-1998004257-A1 PHOSPHATASE INHIBITORS AND METHODS OF USE THEREOF UNIVERSITY OF PITTSBURGH (US) 1998-02-05 — — WO disclosed
US-5700821-A INHIBIT CELL PROLIFERATION UNIVERSITY OF PITTSBURGH (US) 1997-12-23 — — 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 (4 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 34/4885TLR2 3821/4885
US-20240400617-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION KRAS, NRAS, HRAS MDM4 441/4885TP53 34/4885TLR2 3821/4885
US-20240148821-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND VIP, IAPP, KRAS MDM4 1294/4885TP53 178/4885TLR2 4611/4885
US-12371454-B2 Cyclic peptide compound having Kras inhibitory action KRAS, NRAS, HRAS MDM4 441/4885TP53 34/4885TLR2 3821/4885

“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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