SCHEMBL7889307

SCHEMBL7889307

C=CCO[C@H]1O[C@H](CO)[C@@H](OC(=O)c2ccccc2)[C@H](OC(=O)c2ccccc2)[C@@H]1NC(C)=O

nearest known ligand 0.44

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 3/20 0.44
▸ KMT2A Q03164 1/20 0.44
▸ LGALS3 P17931 3/20 0.42
▸ LGALS9 O00182 1/20 0.42
▸ LGALS1 P09382 1/20 0.42
▸ LGALS7; LGALS7B P47929 1/20 0.42
▸ POLB P06746 2/20 0.41
▸ SELP P16109 2/20 0.40
▸ ALDH1A1 P00352 1/20 0.39

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
SCHEMBL14819156 0.92 LGALS3 (0.50) LGALS3LGALS9LGALS1LGALS7; LGALS7BPOLB
SCHEMBL14819208 0.92 LGALS3 (0.50) LGALS3LGALS9LGALS1LGALS7; LGALS7BPOLB
SCHEMBL2483143 0.85 LGALS3 (0.48) LGALS3LGALS9LGALS1LGALS7; LGALS7BSELP
SCHEMBL17241861 0.85 LGALS3 (0.48) LGALS3LGALS9LGALS1LGALS7; LGALS7BSELP
SCHEMBL20226186 0.85 LGALS3 (0.48) LGALS3LGALS9LGALS1LGALS7; LGALS7BSELP
SCHEMBL17241860 0.85 LGALS3 (0.48) LGALS3LGALS9LGALS1LGALS7; LGALS7BSELP
SCHEMBL19613777 0.85 LMNA (0.44) LMNAKMT2ALGALS3LGALS9LGALS1
SCHEMBL5319950 0.84 LMNA (0.43) LMNAKMT2APOLBALDH1A1
SCHEMBL5319948 0.84 LMNA (0.43) LMNAKMT2APOLBALDH1A1
SCHEMBL13367679 0.83 MAPK1 (0.49) LMNAKMT2ALGALS3LGALS9LGALS1

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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6168934-B1 EFFICIENT GLYCOSYLATION BY MIXING ACCEPTOR SACCHARIDE, DONOR MONOSACCHARIDE, ACTIVATING NUCLEOTIDE, ACTIVATED DONOR MONOSACCHARIDE REGENERATING SYSTEM, PYROPHOSPHATE SCAVENGER, AND GLYCOSYLTRANSFERASE IN AN AQUEOUS MEDIUM THE SCRIPPS RESEARCH INSTITUTE 2001-01-02 — — US disclosed
EP-0576592-B1 OLIGOSACCHARIDE ENZYME SUBSTRATES AND INHIBITORS: METHODS AND COMPOSITIONS SCRIPPS RESEARCH INST (US) 2000-05-31 — — EP disclosed
US-5759823-A MIXING IN AQUEOUS MEDIUM ACTIVATED DONOR MONOSACCHARIDE WITH ACCEPTOR SACCHARIDE IN PRESENCE OF GLYCOSYLTRANSFERASE, MAINTAINING TO GLYCOSYLATE ACCEPTOR SACCHARIDE SCRIPPS RESEARCH INSTITUTE (US) 1998-06-02 — — US disclosed
US-5593887-A Oligosaccharide enzyme substrates and inhibitors: methods and compositions THE SCRIPPS RESEARCH INSTITUTE (US) 1997-01-14 — — US disclosed
EP-0576592-A4 OLIGOSACCHARIDE ENZYME SUBSTRATES AND INHIBITORS: METHODS AND COMPOSITIONS SCRIPPS RESEARCH INST (US) 1996-01-24 — — EP disclosed
US-5461143-A Oligosaccharide enzyme substrates and inhibitors: methods and compositions THE SCRIPPS RESEARCH INSTITUTE (US) 1995-10-24 — — US disclosed
EP-0576592-A1 OLIGOSACCHARIDE ENZYME SUBSTRATES AND INHIBITORS: METHODS AND COMPOSITIONS THE SCRIPPS RESEARCH INSTITUTE (US) 1994-01-05 — — EP disclosed
WO-1992016640-A1 OLIGOSACCHARIDE ENZYME SUBSTRATES AND INHIBITORS: METHODS AND COMPOSITIONS THE SCRIPPS RESEARCH INSTITUTE (US) 1992-10-01 — — WO disclosed
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