SCHEMBL6060841

SCHEMBL6060841

CC(=O)O[C@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O

nearest known ligand 0.60

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
▸ SLC28A3 Q9HAS3 4/20 0.50
▸ L3MBTL1 Q9Y468 1/20 0.50
▸ MAPT P10636 1/20 0.49
▸ PYGB P11216 1/20 0.47
▸ LGALS8 O00214 1/20 0.45
▸ GAA P10253 1/20 0.45
▸ TYR P14679 1/20 0.45
▸ CD69 Q07108 1/20 0.45

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
SCHEMBL2429112 1.00 SLC28A3 (0.50) SLC28A3L3MBTL1MAPTPYGBLGALS8
SCHEMBL8361874 1.00 SLC28A3 (0.50) SLC28A3L3MBTL1MAPTPYGBLGALS8
SCHEMBL5862474 1.00 SLC28A3 (0.50) SLC28A3L3MBTL1MAPTPYGBLGALS8
SCHEMBL17523750 1.00 SLC28A3 (0.50) SLC28A3L3MBTL1MAPTPYGBLGALS8
SCHEMBL5199795 1.00 SLC28A3 (0.50) SLC28A3L3MBTL1MAPTPYGBLGALS8
SCHEMBL3144958 1.00 SLC28A3 (0.50) SLC28A3L3MBTL1MAPTPYGBLGALS8
SCHEMBL229613 1.00 SLC28A3 (0.50) SLC28A3L3MBTL1MAPTPYGBLGALS8
SCHEMBL22026379 1.00 SLC28A3 (0.50) SLC28A3L3MBTL1MAPTPYGBLGALS8
SCHEMBL22047951 1.00 SLC28A3 (0.50) SLC28A3L3MBTL1MAPTPYGBLGALS8
SCHEMBL19603336 1.00 SLC28A3 (0.50) SLC28A3L3MBTL1MAPTPYGBLGALS8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5561119-A ANTITUMOR AGENTS LABORATOIRES HOECHST (FR) 1996-10-01 — — US claimed
EP-2737057-B1 NOVEL MARKERS FOR DOPAMINERGIC NEURON PROGENITOR CELLS UNIV KYOTO (JP) 2018-10-24 — — EP disclosed
US-9453840-B2 Markers for dopaminergic neuron progenitor cells KYOTO UNIVERSITY (JP) 2016-09-27 — — US disclosed
US-20140193836-A1 NOVEL MARKERS FOR DOPAMINERGIC NEURON PROGENITOR CELLS EISAI R&D MANAGEMENT CO., LTD. (JP) 2014-07-10 — — US disclosed
EP-2737057-A1 NOVEL MARKERS FOR DOPAMINERGIC NEURON PROGENITOR CELLS Kyoto University (JP) 2014-06-04 — — EP disclosed
WO-2013015457-A1 NOVEL MARKERS FOR DOPAMINERGIC NEURON PROGENITOR CELLS KYOTO UNIVERSITY (JP) 2013-01-31 — — WO disclosed
EP-0987296-B1 A cellulosic composite product and a method of producing the same CANON KK (JP) 2006-12-20 — — EP disclosed
EP-1404691-A2 METHOD FOR PRODUCING PERACYLATED 1-O-GLYCOSIDES SCHERING AKTIENGESELLSCHAFT (DE) 2004-04-07 — — EP disclosed
WO-2003006474-A2 METHOD FOR PRODUCING PERACYLATED 1-O-GLYCOSIDES SCHERING AKTIENGESELLSCHAFT (DE) 2003-01-23 — — WO disclosed
US-6468668-B1 MONOSACCHARIDE DERIVATIVE OR OLIGOSACCHARIDE DERIVATIVE IS REACTION PRODUCT WITH A DIACID, THIS IS REACTED WITH CELLULOSE; BIODEGRADABILITY, RECYCLING PROPERTIES, EXCELLENT MECHANICAL STRENGTH AND MOLD PROCESSABILITY CANON KABUSHIKI KAISHA (JP) 2002-10-22 — — US disclosed
EP-0987296-A1 A cellulosic composite product and a method of producing the same CANON KABUSHIKI KAISHA (JP) 2000-03-22 — — EP disclosed
WO-1999050438-A2 CHROMOGENIC INDOLE DERIVATIVES INALCO S.P.A. (IT) 1999-10-07 — — WO disclosed
EP-0938492-A1 COMBINATORIAL SYNTHESIS OF CARBOHYDRATE LIBRARIES SYNSORB Biotech Inc. (CA) 1999-09-01 — — EP disclosed
WO-1998022487-A1 COMBINATORIAL SYNTHESIS OF CARBOHYDRATE LIBRARIES SYNSORB BIOTECH, INC. (CA) 1998-05-28 — — WO disclosed
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