SCHEMBL1811234

SCHEMBL1811234

CCCCCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)NCCOCCOCC(=O)NCCOCCOC[C]=O)C(=O)O

nearest known ligand 0.72

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
▸ GLP1R P43220 8/20 0.72
▸ NOD1 Q9Y239 11/20 0.55
▸ SLC6A5 Q9Y345 1/20 0.42

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
SCHEMBL13584158 1.00 GLP1R (0.72) GLP1RNOD1SLC6A5
SCHEMBL5954492 1.00 GLP1R (0.72) GLP1RNOD1SLC6A5
SCHEMBL14735663 0.96 GLP1R (0.67) GLP1RNOD1SLC6A5
SCHEMBL14735664 0.96 GLP1R (0.67) GLP1RNOD1SLC6A5
SCHEMBL4152876 0.93 GLP1R (0.65) GLP1RNOD1SLC6A5
SCHEMBL4004880 0.92 GLP1R (0.63) GLP1RNOD1
SCHEMBL15633597 0.92 GLP1R (0.63) GLP1RNOD1
SCHEMBL4541595 0.92 GLP1R (0.63) GLP1RNOD1
SCHEMBL4561886 0.92 GLP1R (0.63) GLP1RNOD1
SCHEMBL2181197 0.92 GLP1R (0.63) GLP1RNOD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3548062-B1 NEW COMPOUNDS AS PEPTIDIC GLP1/GLUCAGON/GIP RECEPTOR AGONISTS SANOFI SA (FR) 2022-01-12 — — EP claimed
EP-3548508-B1 NEW COMPOUNDS AS PEPTIDIC TRIGONAL GLP1/GLUCAGON/GIP RECEPTOR AGONISTS SANOFI SA (FR) 2021-10-27 — — EP claimed
EP-3548062-A1 NEW COMPOUNDS AS PEPTIDIC GLP1/GLUCAGON/GIP RECEPTOR AGONISTS Sanofi (FR) 2019-10-09 — — EP claimed
EP-3548508-A1 NEW COMPOUNDS AS PEPTIDIC TRIGONAL GLP1/GLUCAGON/GIP RECEPTOR AGONISTS Sanofi (FR) 2019-10-09 — — EP claimed
EP-3129397-B1 PEPTIDIC DUAL GLP-1 / GLUCAGON RECEPTOR AGONISTS DERIVED FROM EXENDIN-4 SANOFI SA (FR) 2019-01-09 — — EP claimed
EP-3129395-B1 EXENDIN-4 DERIVATIVES AS PEPTIDIC DUAL GLP-1 / GLUCAGON RECEPTOR AGONISTS SANOFI SA (FR) 2018-12-19 — — EP claimed
WO-2018100134-A1 NEW COMPOUNDS AS PEPTIDIC TRIGONAL GLP1/GLUCAGON/GIP RECEPTOR AGONISTS SANOFI (FR) 2018-06-07 — — WO claimed
WO-2018100135-A1 NEW COMPOUNDS AS PEPTIDIC GLP1/GLUCAGON/GIP RECEPTOR AGONISTS SANOFI (FR) 2018-06-07 — — WO claimed
US-20180155406-A1 COMPOUNDS AS PEPTIDIC TRIGONAL GLP1/GLUCAGON/GIP RECEPTOR AGONISTS SANOFI (FR) 2018-06-07 — — US claimed
US-20180155407-A1 COMPOUNDS AS PEPTIDIC GLP1/GLUCAGON/GIP RECEPTOR AGONISTS SANOFI (FR) 2018-06-07 — — US claimed
EP-3129396-A1 DUAL GLP-1 / GLUCAGON RECEPTOR AGONISTS DERIVED FROM EXENDIN-4 Sanofi (FR) 2017-02-15 — — EP claimed
EP-3129395-A1 EXENDIN-4 DERIVATIVES AS PEPTIDIC DUAL GLP-1 / GLUCAGON RECEPTOR AGONISTS Sanofi (FR) 2017-02-15 — — EP claimed
EP-3129397-A1 PEPTIDIC DUAL GLP-1 / GLUCAGON RECEPTOR AGONISTS DERIVED FROM EXENDIN-4 Sanofi (FR) 2017-02-15 — — EP claimed
US-20150322128-A1 DUAL GLP-1/GLUCAGON RECEPTOR AGONISTS DERIVED FROM EXENDIN-4 SANOFI (FR) 2015-11-12 — — US claimed
US-20150322129-A1 PEPTIDIC DUAL GLP-1/GLUCAGON RECEPTOR AGONISTS DERIVED FROM EXENDIN-4 SANOFI (FR) 2015-11-12 — — US claimed
US-20150315260-A1 EXENDIN-4 DERIVATIVES AS PEPTIDIC DUAL GLP-1/GLUCAGON RECEPTOR AGONISTS SANOFI (FR) 2015-11-05 — — US claimed
WO-2015155141-A1 PEPTIDIC DUAL GLP-1 / GLUCAGON RECEPTOR AGONISTS DERIVED FROM EXENDIN-4 SANOFI (FR) 2015-10-15 — — WO claimed
WO-2015155140-A1 DUAL GLP-1 / GLUCAGON RECEPTOR AGONISTS DERIVED FROM EXENDIN-4 SANOFI (FR) 2015-10-15 — — WO claimed
WO-2015155139-A1 EXENDIN-4 DERIVATIVES AS PEPTIDIC DUAL GLP-1 / GLUCAGON RECEPTOR AGONISTS SANOFI (FR) 2015-10-15 — — WO claimed
EP-2057189-B1 ACYLATED EXENDIN-4 COMPOUNDS NOVO NORDISK AS (DK) 2013-03-06 — — EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 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-20150322128-A1 DUAL GLP-1/GLUCAGON RECEPTOR AGONISTS DERIVED FROM EXENDIN-4 GLP1R, GIPR, GCGR GLP1R 1/4885NOD1 1462/4885SLC6A5 887/4885
US-20150315260-A1 EXENDIN-4 DERIVATIVES AS PEPTIDIC DUAL GLP-1/GLUCAGON RECEPTOR AGONISTS GLP1R, GIPR, GCGR GLP1R 1/4885NOD1 1055/4885SLC6A5 1327/4885
US-20180155406-A1 COMPOUNDS AS PEPTIDIC TRIGONAL GLP1/GLUCAGON/GIP RECEPTOR AGONISTS GLP1R, GIPR, GCGR GLP1R 1/4885NOD1 1688/4885SLC6A5 1720/4885
US-20150322129-A1 PEPTIDIC DUAL GLP-1/GLUCAGON RECEPTOR AGONISTS DERIVED FROM EXENDIN-4 GLP1R, GIPR, GCGR GLP1R 1/4885NOD1 1301/4885SLC6A5 1366/4885
US-20180155407-A1 COMPOUNDS AS PEPTIDIC GLP1/GLUCAGON/GIP RECEPTOR AGONISTS GLP1R, GIPR, GCGR GLP1R 1/4885NOD1 1771/4885SLC6A5 1415/4885

“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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