SCHEMBL7149877

SCHEMBL7149877

C[Si](C)(C)OC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

nearest known ligand 0.64

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 1/20 0.53
▸ MAPT P10636 1/20 0.51
▸ LGALS1 P09382 2/20 0.48
▸ LGALS3 P17931 2/20 0.48
▸ LGALS9 O00182 1/20 0.48
▸ LGALS8 O00214 1/20 0.48
▸ GAA P10253 1/20 0.47
▸ TYR P14679 1/20 0.47
▸ POLB P06746 1/20 0.46
▸ MEN1 O00255 1/20 0.44
▸ KMT2A Q03164 1/20 0.44
▸ ACHE P22303 1/20 0.43

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
SCHEMBL28177022 1.00 L3MBTL1 (0.53) L3MBTL1MAPTLGALS1LGALS3LGALS9
SCHEMBL5514021 1.00 L3MBTL1 (0.53) L3MBTL1MAPTLGALS1LGALS3LGALS9
SCHEMBL22710167 1.00 L3MBTL1 (0.53) L3MBTL1MAPTLGALS1LGALS3LGALS9
SCHEMBL4959971 1.00 L3MBTL1 (0.53) L3MBTL1MAPTLGALS1LGALS3LGALS9
SCHEMBL2510979 0.83 MEN1 (0.48) L3MBTL1MAPTLGALS3LGALS8MEN1
SCHEMBL22659959 0.82 L3MBTL1 (0.47) L3MBTL1MAPTGAATYRPOLB
SCHEMBL5309859 0.82 L3MBTL1 (0.55) L3MBTL1MAPTGAATYRPOLB
SCHEMBL166332 0.79 L3MBTL1 (0.56) L3MBTL1MAPTLGALS8GAATYR
SCHEMBL21847893 0.79 L3MBTL1 (0.56) L3MBTL1MAPTLGALS8GAATYR
SCHEMBL12304019 0.79 L3MBTL1 (0.56) L3MBTL1MAPTLGALS8GAATYR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116730998-A Process for preparing aryl carbon glycoside compound 四川大学华西医院 2023-09-12 — — CN disclosed
CN-111057032-B Preparation method of dapagliflozin 东南大学 2022-03-11 — — CN disclosed
US-6562514-B1 Stabilized vanadium electrolyte solutions for all-vanadium redox cells and batteries PINNACLE VRB LIMITED (AU) 2003-05-13 — — US disclosed
US-6468688-B2 CHARGING, DISCHARGING EFFICIENCY; VANADIUM ELECTROLYTE PINNACLE VRB LIMITED (AU) 2002-10-22 — — US disclosed
US-20010028977-A1 Charging, discharging efficiency; vanadium electrolyte JD HOLDING INC. (KY) 2001-10-11 — — US disclosed
US-6258749-B1 APPLYING WITH PHOTOCATALYST THE DOW CHEMICAL COMPANY 2001-07-10 — — US disclosed
EP-0829104-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) 1998-03-18 — — EP disclosed
EP-0729648-A4 STABILISED ELECTROLYTE SOLUTIONS, METHODS OF PREPARATION THEREOF AND REDOX CELLS AND BATTERIES CONTAINING STABILISED ELECTROLYTE SOLUTIONS UNISEARCH LTD (AU) 1997-01-02 — — EP 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
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
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