SCHEMBL29440225

SCHEMBL29440225

CC(C)C[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](N)CC(=O)O)C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)O

nearest known ligand 0.59

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ TACR1 P25103 1/20 0.59
▸ KISS1R Q969F8 4/20 0.58
▸ NPY1R P25929 1/20 0.58
▸ NPY2R P49146 1/20 0.58
▸ NPY4R P50391 1/20 0.58
▸ NPY5R Q15761 1/20 0.58
▸ CXCR4 P61073 4/20 0.58
▸ CXCL8 P10145 4/20 0.57
▸ GLP1R P43220 6/20 0.56
▸ GIPR P48546 6/20 0.56

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
SCHEMBL30600981 0.98 NPY1R (0.60) TACR1KISS1RNPY1RNPY2RNPY4R
SCHEMBL29949651 0.89 NPY1R (0.67) KISS1RNPY1RNPY2RNPY4RNPY5R
SCHEMBL30414398 0.88 NTSR2 (0.61) TACR1KISS1RCXCR4CXCL8
SCHEMBL29418257 0.88 BACE1 (0.62) KISS1RGLP1RGIPR
SCHEMBL31186286 0.88 KISS1R (0.65) TACR1KISS1RCXCR4CXCL8
SCHEMBL31182571 0.87 NPY2R (0.71) NPY1RNPY2RNPY4RNPY5RCXCR4
SCHEMBL29450205 0.87 CXCL8 (0.62) NPY1RNPY2RNPY4RNPY5RCXCR4
SCHEMBL30598998 0.87 C5AR1 (0.58) KISS1RNPY1RNPY2RNPY4RNPY5R
SCHEMBL29533335 0.86 TACR1 (0.62) TACR1KISS1RCXCR4CXCL8
SCHEMBL28737909 0.86 TACR1 (0.62) TACR1KISS1RCXCR4CXCL8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025217401-A1 A PEPTIDE INHIBITOR OF THE EYA AND PP2A-B55A INTERACTION USEFUL FOR MYC-DRIVEN CANCER THERAPY THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE (US) 2025-10-16 — — WO claimed
EP-4077353-B1 SYNTHESIS OF AMANIN AND ITS DERIVATIVES HEIDELBERG PHARMA RES GMBH (DE) 2025-04-23 — — EP claimed
US-20240173256-A1 HDL MIMICKING TARGETED DRUG DELIVERY SYSTEM FOR THE TREATMENT OF SOLID TUMORS UNIVERSITY OF NORTH TEXAS HEALTH SCIENCE CENTER (US) 2024-05-30 — — US claimed
CN-115666653-A Antibody-drug conjugates 斯皮雷亚有限公司 2023-01-31 — — CN claimed
CN-115472234-A Hidden variable Gaussian process soft measurement modeling method integrating qualitative and quantitative information 浙江工业大学 2022-12-13 — — CN claimed
CN-114599389-A Variant FC domains and uses thereof 奇达拉治疗公司 2022-06-07 — — CN claimed
US-20260062455-A1 UPTAKE MECHANISM OF ESSENTIAL LYSOPHOSPHOLIPIDS INTO THE BRAIN AND INHIBITION BY ENDOGENOUS-RETROVIRAL ENVELOPE PROTEIN PASTEUR INSTITUT (FR) 2026-03-05 — — US disclosed
US-12467928-B2 N-terminal modifier agents and binders for treating and analyzing peptides DF PEPTIDE ACQUISITION LLC 2025-11-11 — — US disclosed
US-12467049-B2 Methods and kits using nucleic acid encoding and/or label DF PEPTIDE ACQUISITION LLC 2025-11-11 — — US disclosed
EP-4637797-A1 METHOD FOR OBTAINING AN EXTRACT OF PLANT ORIGIN, A COMPOSITION CONTAINING IT AND ITS COSMETIC USE SEDERMA (FR) 2025-10-29 — — EP disclosed
US-20250295742-A1 PHENYLALANINE-DEGRADING ENZYME VARIANTS AND TREATMENTS FOR PHENYLKETONURIA IDITAROD BIO, INC. (US) 2025-09-25 — — US disclosed
WO-2025128687-A1 GLUCOSE-DEPENDENT DROPLETS AND SUPRAMOLECULAR PEPTIDE DEPOTS FOR GLUCOSE-RESPONSIVE GLUCAGON DELIVERY UNIVERSITY OF NOTRE DAME DU LAC (US) 2025-06-19 — — WO disclosed
US-12319752-B2 Heparin-binding cationic peptide self-assembling peptide amphiphiles useful against drug-resistant bacteria NORTHEASTERN UNIVERSITY (US) 2025-06-03 — — US disclosed
CN-114302735-A Peptide inhibitors of HIV capsid inhibition 密苏里大学管理者 2022-04-08 — — CN disclosed
WO-2022072560-A1 POLYPEPTIDE TERMINAL BINDERS AND USES THEREOF Encodia, Inc. (US) 2022-04-07 — — WO disclosed
EP-3966326-A1 FMRP AND CANCER TREATMENT ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE (EPFL) (CH) 2022-03-16 — — EP disclosed
US-11274131-B2 IgM-mediated receptor clustering and cell modulation MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2022-03-15 — — US disclosed
CN-114174338-A Antibodies that bind to GPRC5D 豪夫迈·罗氏有限公司 2022-03-11 — — CN disclosed
CN-114174342-A Antibodies that bind to GPRC5D 豪夫迈·罗氏有限公司 2022-03-11 — — CN disclosed
CN-114127123-A Fusion of CEA-binding antibodies to 4-1BBL 豪夫迈·罗氏有限公司 2022-03-01 — — 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 (2 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-12319752-B2 Heparin-binding cationic peptide self-assembling peptide amphiphiles useful against drug-resistant bacteria NGLY1, HM13, VIP TACR1 1973/4885KISS1R 2271/4885NPY1R 3148/4885
US-20260062455-A1 UPTAKE MECHANISM OF ESSENTIAL LYSOPHOSPHOLIPIDS INTO THE BRAIN AND INHIBITION BY ENDOGENOUS-RETROVIRAL ENVELOPE PROTEIN SNAP29, SLC18A2, NSF TACR1 3397/4885KISS1R 1209/4885NPY1R 2581/4885

“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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