Exenatide

Exenatide

SCHEMBL29350782

CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(=O)O)NC(=O)CNC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)NCC(=O)NCC(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(N)=O

nearest known ligand 0.86

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GLP1R

The experimentally established mechanism targets of Exenatide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
▸ GLP1R known ✓ P43220 14/20 0.86
▸ GCGR P47871 11/20 0.74
▸ GIPR P48546 6/20 0.74
▸ CCKBR P32239 1/20 0.73
▸ NPY1R P25929 1/20 0.72
▸ NPY2R P49146 1/20 0.72
▸ NPY4R P50391 1/20 0.72
▸ NPY5R Q15761 1/20 0.72
▸ PTH1R Q03431 1/20 0.72

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
Exenatide SCHEMBL29827241 0.95 GLP1R (0.81) GLP1RGCGRGIPRCCKBR
Exenatide SCHEMBL29710890 0.95 GLP1R (0.81) GLP1RGCGRGIPRCCKBR
Exenatide SCHEMBL14634818 0.95 GLP1R (0.81) GLP1RGCGRGIPRCCKBR
SCHEMBL29429437 0.95 GLP1R (0.81) GLP1RGCGRGIPRCCKBR
Exenatide SCHEMBL20509814 0.95 GLP1R (0.81) GLP1RGCGRGIPRCCKBR
SCHEMBL31072728 0.95 GLP1R (0.81) GLP1RGCGRGIPRCCKBR
Exenatide SCHEMBL30947451 0.95 GLP1R (0.79) GLP1RGCGRGIPR
Exenatide SCHEMBL28285812 0.95 GLP1R (0.82) GLP1RGCGRGIPRCCKBR
Exenatide SCHEMBL28323280 0.95 GLP1R (0.81) GLP1RGCGRGIPRCCKBR
Exenatide SCHEMBL29503493 0.94 GLP1R (0.80) GLP1RGCGRGIPRCCKBR

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

Appears in 6897 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3594323-B1 METHODS AND COMPOSITIONS FOR GENERATING PANCREATIC PROGENITORS AND FUNCTIONAL BETA CELLS FROM HPSCS UNIV HEALTH NETWORK (CA) 2026-05-27 — — EP claimed
US-12630803-B2 Method of increasing proliferation of pancreatic beta cells, treatment method, and composition ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (US) 2026-05-19 — — US claimed
CN-122038275-A Method for inducing mesenchymal stem cells to differentiate into islet-like cells and application thereof 天津市康婷生物工程集团有限公司 2026-05-15 — — CN claimed
US-12622947-B2 Pharmaceutical composition for treating levodopa-induced dyskinesia or for suppressing progression thereof PEPTRON, INC. (KR) 2026-05-12 — — US claimed
US-20260124148-A1 POLYPEPTIDE FORMULATIONS FOR ORAL DELIVERY BHAMIS RES LABORATORY PVT LTD (IN) 2026-05-07 — — US claimed
EP-4733314-A1 NOVEL BISPECIFIC FUSION PROTEIN AND USE THEREOF Slbigen Inc. (KR) 2026-04-29 — — EP claimed
EP-3634453-B1 PLANT EXTRACTS WITH ANTI-DIABETIC AND OTHER USEFUL ACTIVITIES HOUSEY PHARMACEUTICAL RES LABORATORIES L L C (US) 2026-04-29 — — EP claimed
EP-4720107-A1 A FUSION PEPTIDE FOR ACTIVATION OF THE APJ AND / OR GLP-1 RECEPTORS University Of Ulster (GB) 2026-04-08 — — EP claimed
US-12594303-B2 Composition comprising exosomes derived from induced pluripotent stem cell-derived mesenchymal stem cell progenitor for prevention or treatment of non-alcoholic steatohepatitis BREXOGEN INC. (KR) 2026-04-07 — — US claimed
EP-4714494-A2 A MYOSTATIN PATHWAY INHIBITOR IN COMBINATION WITH A GLP-1 PATHWAY ACTIVATOR FOR USE IN TREATING METABOLIC DISORDERS Scholar Rock, Inc. (US) 2026-03-25 — — EP claimed
US-11261227-B2 Glucagon derivative and a composition comprising a long acting conjugate of the same HANMI PHARM. CO., LTD. (KR) 2022-03-01 — — US claimed
EP-3955913-A1 COMPOSITIONS AND METHODS FOR TREATING DIABETES ENZYCHEM LIFESCIENCES (KR) 2022-02-23 — — EP claimed
US-11254916-B2 Methods of making and using PDX1-positive pancreatic endoderm cells VIACYTE, INC. (US) 2022-02-22 — — US claimed
CN-114053217-A Exendin-4-Fc fusion protein injection preparation and preparation method thereof 华兰生物工程股份有限公司 2022-02-18 — — CN claimed
WO-2022034062-A1 EXENDIN-4 PEPTIDE ANALOGUES TXP PHARMA AG (CH) 2022-02-17 — — WO claimed
CN-109486770-B Method for promoting directional differentiation of human iPS into islet beta cells by using microRNA-181c-5p 深圳市人民医院 2022-02-11 — — CN claimed
WO-2022029231-A1 SOLUBLE NPY2 RECEPTOR AGONISTS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2022-02-10 — — WO claimed
CN-114025776-A Composition for preventing or treating nonalcoholic steatohepatitis comprising exosomes derived from induced pluripotent stem cell-derived mesenchymal stem cell precursor cells 布瑞克斯奥根株式会社 2022-02-08 — — CN claimed
WO-2022025559-A1 COMPOSITION INCLUDING STEM CELL-DERIVED EXOSOME, AND METHOD FOR PRODUCING SAME 브렉소젠 주식회사 2022-02-03 — — WO claimed
US-20220025011-A1 LONG-ACTING EXENDIN-4 AND USE THEREOF INDUSTRY-ACADEMIC COOPERATION FOUNDATION GYEONGSANG NATIONAL UNIVERSITY (KR) 2022-01-27 — — US claimed
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