SCHEMBL358953

SCHEMBL358953

NCC(=O)N[C@@H](CS)C(=O)O

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 0.57
MAPT P10636 1/20 0.57
THRB P10828 1/20 0.57
ALOX15 P16050 1/20 0.57
NFKB1 P19838 1/20 0.57
PTGS2 P35354 1/20 0.57
THPO P40225 1/20 0.57
RECQL P46063 1/20 0.57
BLM P54132 1/20 0.57
SMN1; SMN2 Q16637 1/20 0.57
ACE P12821 1/20 0.52
FOLH1 Q04609 1/20 0.48
FNTA P49354 3/20 0.43
FNTB P49356 3/20 0.43
CA2 P00918 4/20 0.42
CA1 P00915 3/20 0.42
PTGS1 P23219 2/20 0.41
GSTK1 Q9Y2Q3 1/20 0.41
SLC7A11 Q9UPY5 1/20 0.39
GNPAT O15228 1/20 0.37

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
SCHEMBL30051376 1.00 KDM4E (0.57) KDM4EMAPTTHRBALOX15NFKB1
SCHEMBL1983976 1.00 KDM4E (0.57) KDM4EMAPTTHRBALOX15NFKB1
SCHEMBL28767097 0.98 KDM4E (0.55) KDM4EMAPTTHRBALOX15NFKB1
SCHEMBL929660 0.92 ACE (0.55) KDM4EMAPTTHRBALOX15NFKB1
Cysteine SCHEMBL27656948 0.91 PTGS1 (0.57) KDM4EMAPTTHRBALOX15NFKB1
SCHEMBL29702215 0.88 ACE (0.50) KDM4EMAPTTHRBALOX15NFKB1
SCHEMBL7790449 0.87 KDM4E (0.48) KDM4EMAPTTHRBALOX15NFKB1
SCHEMBL7790453 0.87 KDM4E (0.48) KDM4EMAPTTHRBALOX15NFKB1
SCHEMBL29567569 0.86 PTGS1 (0.54) KDM4EMAPTTHRBALOX15NFKB1
SCHEMBL25774753 0.86 ACE (0.49) KDM4EMAPTTHRBALOX15NFKB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4627103-A1 IMPEDIMETRIC DETECTION USING PEPTIDE AND PEPTIDE MIXTURES Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. (IL) 2025-10-08 EP claimed
EP-4536265-A2 TREATMENTS FOR DISEASES AND DISORDERS THAT INVOLVE OXIDATIVE STRESS Jenius Pharma, LLC (US) 2025-04-16 EP claimed
US-12129277-B2 Linear solution phase routes for WNT hexapeptides WNTRESEARCH AB (SE) 2024-10-29 US claimed
EP-4389216-A2 PEPTIDE COMPOSITIONS AND THERAPEUTIC USES Allegro Pharmaceuticals, LLC (US) 2024-06-26 EP claimed
WO-2024116168-A1 IMPEDIMETRIC DETECTION USING PEPTIDE AND PEPTIDE MIXTURES YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM LTD. (IL) 2024-06-06 WO claimed
CN-113646324-B Linear solution phase pathway for WNT hexapeptide 温特研究公司 2024-03-29 CN claimed
US-20240101714-A1 ASSEMBLY OF BISPECIFIC ANTIBODIES GENENTECH INC (US) 2024-03-28 US claimed
CN-111285921-B BDK auxiliary group and liquid phase total synthesis method of procalcitonin and analog based on BDK auxiliary group 西北工业大学 2024-03-01 CN claimed
US-11912791-B2 Solution phase routes for Wnt hexapeptides WNTRESEARCH AB (SE) 2024-02-27 US claimed
WO-2023239716-A2 TREATMENTS FOR DISEASES AND DISORDERS THAT INVOLVE OXIDATIVE STRESS Allegro Pharmaceuticals, LLC (US) 2023-12-14 WO 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-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-5635170-A N-GLYCINE-L-CYSTEINE AND/OR L-CYSTEINE-N-GLYCINE IS USED AS HAIR KERATIN REDUCING AGENT WELLA AKTIENGESELLCHAFT (DE) 1997-06-03 US 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