Maltitol

Maltitol

SCHEMBL7149629

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

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ L3MBTL1 Q9Y468 1/20 0.41
▸ PPARG P37231 1/20 0.41
▸ PPARD Q03181 1/20 0.41
▸ PPARA Q07869 1/20 0.41
▸ MEN1 O00255 1/20 0.40
▸ KMT2A Q03164 1/20 0.40
▸ GAA P10253 2/20 0.40
▸ MAPT P10636 2/20 0.40
▸ TYR P14679 1/20 0.40
▸ CD209 Q9NNX6 2/20 0.40
▸ PTPN1 P18031 1/20 0.40
▸ SYNJ2 O15056 2/20 0.39
▸ KDM4E B2RXH2 1/20 0.39
▸ ABL1 P00519 1/20 0.39
▸ ALPL P05186 1/20 0.39
▸ POLB P06746 1/20 0.39
▸ ALPI P09923 1/20 0.39
▸ ALPG P10696 1/20 0.39
▸ PABPC1 P11940 1/20 0.39
▸ RECQL P46063 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
Maltitol SCHEMBL3708375 1.00 L3MBTL1 (0.41) L3MBTL1PPARGPPARDPPARAMEN1
Maltitol SCHEMBL18744689 1.00 L3MBTL1 (0.41) L3MBTL1PPARGPPARDPPARAMEN1
Maltitol SCHEMBL8600577 1.00 L3MBTL1 (0.41) L3MBTL1PPARGPPARDPPARAMEN1
Maltitol SCHEMBL13024834 1.00 L3MBTL1 (0.41) L3MBTL1PPARGPPARDPPARAMEN1
Maltitol SCHEMBL18744690 1.00 L3MBTL1 (0.41) L3MBTL1PPARGPPARDPPARAMEN1
Maltitol SCHEMBL13912565 1.00 L3MBTL1 (0.41) L3MBTL1PPARGPPARDPPARAMEN1
Maltitol SCHEMBL21947405 1.00 L3MBTL1 (0.41) L3MBTL1PPARGPPARDPPARAMEN1
Maltitol SCHEMBL21947406 1.00 L3MBTL1 (0.41) L3MBTL1PPARGPPARDPPARAMEN1
Maltitol SCHEMBL22516409 1.00 L3MBTL1 (0.41) L3MBTL1PPARGPPARDPPARAMEN1
Maltitol SCHEMBL16153886 1.00 L3MBTL1 (0.41) L3MBTL1PPARGPPARDPPARAMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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-6143443-A ALL-VANADIUM REDOX BATTERY, COMPRISING THE STABILIZED ELECTROLYTE PINNACLE ARB LIMITED (AU) 2000-11-07 — — 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
US-5641872-A USING AN HYDROGENATION CATALYST COMPRISING A PRESSED POWDER ALLOY OF AT LEAST THREE METALS; IN AQUEOUS SOLUTION AT ELEVATED TEMPERATURE AND PRESSURE BAYER AKTIENGESELLSCHAFT (DE) 1997-06-24 — — US 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
EP-0423525-B1 PROCESS FOR THE PREPARATION OF EPIMER-FREE SUGARALCOHOLS FROM THE GROUP OF XYLITOL, SORBITOL (D-GLUCITOL), 4-0-BETA-D-GALACTOPYRANOSYL-D-GLUCITOL AND 4-0-ALPHA-D-GLYCOPYRANOSYL-D-SORBITOL BAYER AG (DE) 1993-06-23 — — EP disclosed
US-5162517-A Process for the preparation of epimer-free sugar alcohols from the group consisting of xylitol, sorbitol (D-glucitol), 4-O-β-D-galactopyranosyl-D-glucitol and 4-O-α-D-glucopyranosyl-D-sorbitol BAYER AKTIENGESELLSCHAFT (DE) 1992-11-10 — — US disclosed
EP-0423525-A1 Process for the preparation of epimer-free sugaralcohols from the group of xylitol, sorbitol (D-glucitol), 4-0-beta-D-galactopyranosyl-D-glucitol and 4-0-alpha-D-glycopyranosyl-D-sorbitol BAYER AG (DE) 1991-04-24 — — EP disclosed
Send feedback