SCHEMBL7887064

SCHEMBL7887064

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

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 3/20 0.59
▸ POLB P06746 2/20 0.59
▸ ALDH1A1 P00352 2/20 0.59
▸ KMT2A Q03164 1/20 0.57
▸ CYP3A4 P08684 2/20 0.55
▸ MAPT P10636 1/20 0.55
▸ CYP2C9 P11712 1/20 0.55
▸ CYP2C19 P33261 1/20 0.55
▸ KDM4E B2RXH2 1/20 0.48
▸ CYP2D6 P10635 2/20 0.47
▸ THRB P10828 1/20 0.47
▸ HSD17B10 Q99714 1/20 0.47
▸ CA2 P00918 5/20 0.43
▸ CA1 P00915 4/20 0.43
▸ CA9 Q16790 4/20 0.43
▸ CA12 O43570 3/20 0.43
▸ TGM2 P21980 1/20 0.42
▸ TSHR P16473 1/20 0.41
▸ NR3C1 P04150 1/20 0.41
▸ FYN P06241 1/20 0.41

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
SCHEMBL20516507 1.00 LMNA (0.59) LMNAPOLBALDH1A1KMT2ACYP3A4
SCHEMBL20788118 1.00 LMNA (0.59) LMNAPOLBALDH1A1KMT2ACYP3A4
SCHEMBL13646612 1.00 LMNA (0.59) LMNAPOLBALDH1A1KMT2ACYP3A4
SCHEMBL7887070 1.00 LMNA (0.59) LMNAPOLBALDH1A1KMT2ACYP3A4
SCHEMBL13650799 1.00 LMNA (0.59) LMNAPOLBALDH1A1KMT2ACYP3A4
SCHEMBL13038857 1.00 LMNA (0.59) LMNAPOLBALDH1A1KMT2ACYP3A4
SCHEMBL14468743 1.00 LMNA (0.59) LMNAPOLBALDH1A1KMT2ACYP3A4
SCHEMBL23069384 0.89 LMNA (0.62) LMNAPOLBALDH1A1KMT2ACYP3A4
SCHEMBL10719671 0.89 LMNA (0.53) LMNAPOLBALDH1A1KMT2ACYP3A4
SCHEMBL21195779 0.88 LMNA (0.47) LMNAPOLBALDH1A1KMT2ACYP3A4

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 7 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
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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