SCHEMBL5026360

SCHEMBL5026360

OC[C@H]1O[C@H](OCc2ccccc2)[C@H](O)[C@@H](O)[C@H]1O

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ SLC6A2 P23975 2/20 0.57
▸ SYNJ2 O15056 2/20 0.56
▸ KDM4E B2RXH2 1/20 0.56
▸ ABL1 P00519 1/20 0.56
▸ ALPL P05186 1/20 0.56
▸ POLB P06746 1/20 0.56
▸ ALPI P09923 1/20 0.56
▸ GAA P10253 1/20 0.56
▸ MAPT P10636 1/20 0.56
▸ ALPG P10696 1/20 0.56
▸ PABPC1 P11940 1/20 0.56
▸ RECQL P46063 1/20 0.56
▸ GALK1 P51570 1/20 0.56
▸ CASP7 P55210 1/20 0.56
▸ CASP6 P55212 1/20 0.56
▸ MCL1 Q07820 1/20 0.56
▸ RIN1 Q13671 1/20 0.56
▸ EIF4H Q15056 1/20 0.56
▸ SLC5A2 P31639 1/20 0.54
▸ TYR P14679 1/20 0.54

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
SCHEMBL9001318 1.00 SLC6A2 (0.57) SLC6A2SYNJ2KDM4EABL1ALPL
SCHEMBL8838912 1.00 SLC6A2 (0.57) SLC6A2SYNJ2KDM4EABL1ALPL
SCHEMBL18718056 1.00 SLC6A2 (0.57) SLC6A2SYNJ2KDM4EABL1ALPL
SCHEMBL9155988 1.00 SLC6A2 (0.57) SLC6A2SYNJ2KDM4EABL1ALPL
SCHEMBL20056672 1.00 SLC6A2 (0.57) SLC6A2SYNJ2KDM4EABL1ALPL
SCHEMBL15504372 1.00 SLC6A2 (0.57) SLC6A2SYNJ2KDM4EABL1ALPL
SCHEMBL117781 1.00 SLC6A2 (0.57) SLC6A2SYNJ2KDM4EABL1ALPL
SCHEMBL9849387 1.00 SLC6A2 (0.57) SLC6A2SYNJ2KDM4EABL1ALPL
SCHEMBL5026366 1.00 SLC6A2 (0.57) SLC6A2SYNJ2KDM4EABL1ALPL
SCHEMBL18733414 1.00 SLC6A2 (0.57) SLC6A2SYNJ2KDM4EABL1ALPL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109912642-A Method for stereoselective synthesis of β -2-deoxyglycosidic bond 四川轻化工大学 2019-06-21 — — CN disclosed
EP-3116886-A1 HEXOSE DERIVATIVES, PREPARATION AND USES THEREOF Faculdade De Ciências da Universidade de Lisboa (PT) 2017-01-18 — — EP disclosed
WO-2015137838-A1 HEXOSE DERIVATIVES, PREPARATION AND USES THEREOF EXTREMOCHEM, LDA. (PT) 2015-09-17 — — WO disclosed
US-8389565-B2 Antidiabetic agents; controlling carbohydrate metabolism SIMON FRASER UNIVERSITY (CA) 2013-03-05 — — US disclosed
CN-101165047-B Glycolipid derivative and its manufacturing method, and its synthesizing intermediate and its manufacturing method DAIICHI ASUBIO PHARMA CO LTD (JP) 2010-10-20 — — CN disclosed
CN-100537585-C Glycolipid derivative, process for producing the same, intermediate for the synthesis thereof, and process for producing the same DAIICHI SUNTORY PHARMA CO LTD (JP) 2009-09-09 — — CN disclosed
CN-101437809-A Glycosidase inhibitors and methods of synthesizing same UNIV FRASER SIMON (CA) 2009-05-20 — — CN disclosed
EP-1999124-A1 GLYCOSIDASE INHIBITORS AND METHODS OF SYNTHESIZING SAME SIMON FRASER UNIVERSITY (CA) 2008-12-10 — — EP disclosed
CN-101165047-A Glycolipid derivative and its manufacturing method, and its synthesizing intermediate and its manufacturing method DAIICHI ASUBIO PHARMA CO LTD (JP) 2008-04-23 — — CN disclosed
WO-2007098597-A1 GLYCOSIDASE INHIBITORS AND METHODS OF SYNTHESIZING SAME SIMON FRASER UNIVERSITY (CA) 2007-09-07 — — WO disclosed
WO-1996035239-A1 HIGH ENERGY DENSITY VANADIUM ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND ALL-VANADIUM REDOX CELLS AND BATTERIES CONTAINING HIGH ENERGY VANADIUM ELECTROLYTE SOLUTIONS UNISEARCH LIMITED (AU) 1996-11-07 — — WO disclosed
EP-0729648-A1 STABILISED ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND REDOX CELLS AND BATTERIES CONTAINING STABILISED ELECTROLYTE SOLUTIONS UNISEARCH LIMITED (AU) 1996-09-04 — — EP disclosed
EP-0456948-B1 Method for the preparation of polyphosphorylated derivatives of galactopyranosides with a potential insulin-like activity EUROPHARMA SA (ES) 1995-08-30 — — EP disclosed
WO-1995012219-A1 STABILISED ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND REDOX CELLS AND BATTERIES CONTAINING STABILISED ELECTROLYTE SOLUTIONS UNISEARCH LIMITED (AU) 1995-05-04 — — WO disclosed
EP-0650492-A1 REDUCING INFLAMMATION BY TIME DEPENDENT ADMINISTRATION OF OLIGOSACCHARIDES GLYCOSIDES RELATED TO BLOOD GROUP DETERMINANTS ALBERTA RESEARCH COUNCIL (CA) 1995-05-03 — — EP disclosed
EP-0643718-A1 IMMUNOSUPPRESSIVE AND TOLEROGENIC MODIFIED LEWIS?C AND LacNAc COMPOUNDS ALBERTA RESEARCH COUNCIL (CA) 1995-03-22 — — EP disclosed
EP-0591254-A1 IMMUNOSUPPRESSIVE AND TOLEROGENIC MODIFIED LEWIS?X AND LEWIS?A COMPOUNDS GLYCOMED INCORPORATED (US) 1994-04-13 — — EP disclosed
WO-1993024506-A1 IMMUNOSUPPRESSIVE AND TOLEROGENIC MODIFIED LEWISC AND LacNAc COMPOUNDS ALBERTA RESEARCH COUNCIL (CA) 1993-12-09 — — WO disclosed
WO-1993024505-A1 REDUCING INFLAMMATION BY TIME DEPENDENT ADMINISTRATION OF OLIGOSACCHARIDES GLYCOSIDES RELATED TO BLOOD GROUP DETERMINANTS ALBERTA RESEARCH COUNCIL (CA) 1993-12-09 — — WO disclosed
WO-1992022564-A1 IMMUNOSUPPRESSIVE AND TOLEROGENIC MODIFIED LEWISX AND LEWISA COMPOUNDS ALBERTA RESEARCH COUNCIL (CA) 1992-12-23 — — WO disclosed
Send feedback