SCHEMBL2123083

SCHEMBL2123083

NCCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)O

nearest known ligand 0.65

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
DPP7 Q9UHL4 6/20 0.65
DPP4 P27487 4/20 0.65
DPP8 Q6V1X1 4/20 0.65
DPP9 Q86TI2 2/20 0.65
FAP Q12884 1/20 0.65
ACE P12821 2/20 0.54
REN P00797 1/20 0.52

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
SCHEMBL2123080 1.00 DPP7 (0.65) DPP7DPP4DPP8DPP9FAP
SCHEMBL27796855 1.00 DPP7 (0.65) DPP7DPP4DPP8DPP9FAP
SCHEMBL2113410 1.00 DPP7 (0.65) DPP7DPP4DPP8DPP9FAP
SCHEMBL2113409 1.00 DPP7 (0.65) DPP7DPP4DPP8DPP9FAP
SCHEMBL29374265 1.00 DPP7 (0.65) DPP7DPP4DPP8DPP9FAP
SCHEMBL2113944 0.96 DPP4 (0.59) DPP7DPP4DPP8DPP9FAP
SCHEMBL29610030 0.96 DPP4 (0.59) DPP7DPP4DPP8DPP9FAP
SCHEMBL2113947 0.96 DPP4 (0.59) DPP7DPP4DPP8DPP9FAP
SCHEMBL11017609 0.95 DPP7 (0.60) DPP7DPP4DPP8DPP9FAP
SCHEMBL10829152 0.95 DPP7 (0.60) DPP7DPP4DPP8DPP9FAP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3787631-B1 MODULATORS OF ORPHAN NUCLEAR RECEPTORS FOR NASH AND OTHER METABOLIC DISORDERS UNIV EMORY (US) 2025-09-10 EP claimed
CN-119015834-A Carbon dioxide separation membrane and preparation method thereof 国家能源投资集团有限责任公司 2024-11-26 CN claimed
EP-0618235-B1 Process for the synthesis of semisynthetic glycosaminoglycans containing alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN SPA (IT) 1997-07-23 EP claimed
EP-0565862-B1 Semi-synthetic glycosaminoglycans containing alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN SPA (IT) 1997-06-18 EP claimed
EP-0565863-B1 Semi-synthetic glycosaminoglycans with heparin or heparan structure of alpha-L-iduronic-2-0-sulfate acid modified in position 2 ALFA WASSERMANN SPA (IT) 1997-06-18 EP claimed
EP-0618234-B1 Process for the synthesis of semisynthetic glycosaminoglycans with heparin or heparan structure modified in position 2 of the alpha-L-iduronic-2-0-sulfate acid ALFA WASSERMANN SPA (IT) 1997-06-04 EP claimed
US-5430133-A Semi-synthetic glycosaminoglycans with heparin or heparan structure of α-L-iduronic-2-O-sulfate acid modified in position 2 ALFA WASSERMANN S.P.A. (IT) 1995-07-04 US claimed
US-5410039-A Process for the synthesis of glycosaminoglycans containing α-L-galacturonic acid substituted with nucleophilic groups in position 3 ALFA WASSERMANN S.P.A. (IT) 1995-04-25 US claimed
US-5405949-A Process for the synthesis of glycosaminoglycans with heparin or heparan structure modified in position 2 of the α-L-iduronic-2-O-sulfate acid ALFA WASSERNANN S.P.A. (IT) 1995-04-11 US claimed
EP-0618235-A1 Process for the synthesis of semisynthetic glycosaminoglycans containig alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN S.p.A. (IT) 1994-10-05 EP claimed
EP-0618234-A1 Process for the synthesis of semisynthetic glycosaminoglycans with heparin or heparan structure modified in position 2 of the alpha-L-iduronic-2-0-sulfate acid ALFA WASSERMANN S.p.A. (IT) 1994-10-05 EP claimed
EP-0565863-A2 Semi-synthetic glycosaminoglycans with heparin or heparan structure of alpha-L-iduronic-2-0-sulfate acid modified in position 2 ALFA WASSERMANN S.p.A. (IT) 1993-10-20 EP claimed
EP-0565862-A2 Semi-synthetic glycosaminoglycans containing alpha-L-galacturonic acid substituted with nucleophilic radicals in position 3 ALFA WASSERMANN S.p.A. (IT) 1993-10-20 EP claimed
US-4786737-A PREPARATION OF TUFTSIN AND LISINOPRIL AJINOMOTO CO., INC. (JP) 1988-11-22 US claimed
EP-3526196-B1 ARYL AND HETEROARYL ETHER DERIVATIVES AS LIVER X RECEPTOR BETA AGONISTS MERCK SHARP & DOHME LLC (US) 2026-03-18 EP disclosed
US-12570729-B2 Antibody fragment based antifungal conjugate selectively targeting candida ABGENICS LIFESCIENCES PRIVATE LIMITED (IN) 2026-03-10 US disclosed
EP-4702045-A1 GLUCOSE SENSITIVE INSULIN DERIVATIVES Novo Nordisk A/S (DK) 2026-03-04 EP disclosed
EP-0292708-A2 Detection of Bacteroides gingivalis THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 1988-11-30 EP disclosed
US-4786737-A PREPARATION OF TUFTSIN AND LISINOPRIL AJINOMOTO CO., INC. (JP) 1988-11-22 US disclosed
US-4720554-A Aromatic sulfonic acid salts of a proline derivative AJINOMOTO CO., INC. (JP) 1988-01-19 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 (1 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-12570729-B2 Antibody fragment based antifungal conjugate selectively targeting candida SERPINH1, HM13, NGLY1 DPP7 545/4885DPP4 671/4885DPP8 857/4885

“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.