SCHEMBL1682180

SCHEMBL1682180

CO[C@H]1O[C@H](COC(=O)c2ccccc2)[C@H](O)[C@H](OC(=O)c2ccccc2)[C@H]1OC(=O)c1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
LGALS3 P17931 5/20 0.52
LGALS4 P56470 4/20 0.52
LGALS9 O00182 1/20 0.49
LGALS1 P09382 1/20 0.49
LGALS7; LGALS7B P47929 1/20 0.49
PTPN1 P18031 5/20 0.48
MEN1 O00255 1/20 0.45
USP2 O75604 1/20 0.45
POLB P06746 1/20 0.45
KMT2A Q03164 1/20 0.45
LGALS8 O00214 2/20 0.45
ALDH1A1 P00352 3/20 0.45
PTPN2 P17706 1/20 0.43
PTPN11 Q06124 1/20 0.43
HTT P42858 1/20 0.43
SYNJ2 O15056 3/20 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
SCHEMBL1521368 1.00 LGALS3 (0.52) LGALS3LGALS4LGALS9LGALS1LGALS7; LGALS7B
SCHEMBL12807943 1.00 LGALS3 (0.52) LGALS3LGALS4LGALS9LGALS1LGALS7; LGALS7B
SCHEMBL1682156 1.00 LGALS3 (0.52) LGALS3LGALS4LGALS9LGALS1LGALS7; LGALS7B
SCHEMBL9545439 1.00 LGALS3 (0.52) LGALS3LGALS4LGALS9LGALS1LGALS7; LGALS7B
SCHEMBL12595600 1.00 LGALS3 (0.52) LGALS3LGALS4LGALS9LGALS1LGALS7; LGALS7B
SCHEMBL24192986 1.00 LGALS3 (0.52) LGALS3LGALS4LGALS9LGALS1LGALS7; LGALS7B
SCHEMBL14413230 1.00 LGALS3 (0.52) LGALS3LGALS4LGALS9LGALS1LGALS7; LGALS7B
SCHEMBL19869143 1.00 LGALS3 (0.52) LGALS3LGALS4LGALS9LGALS1LGALS7; LGALS7B
SCHEMBL7150482 0.93 LGALS8 (0.53) LGALS3LGALS4LGALS9LGALS1LGALS7; LGALS7B
SCHEMBL8658236 0.93 LGALS3 (0.46) LGALS3LGALS4LGALS9LGALS1LGALS7; LGALS7B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100267940-A1 Method for Producing 4-Deoxy-4-Fluoro-D-Glucose Derivative CENTRAL GLASS COMPANY, LIMITED (JP) 2010-10-21 US claimed
EP-2216337-A1 METHOD FOR PRODUCING 4-DEOXY-4-FLUORO-D-GLUCOSE DERIVATIVE Central Glass Company, Limited (JP) 2010-08-11 EP claimed
CN-113015432-B Compositions comprising sulfated galactose and embodiments thereof SEA6能源私人有限公司 2024-03-26 CN disclosed
US-10174132-B2 Heparan sulfate synthesis UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2019-01-08 US disclosed
US-20160060365-A1 HEPARAN SULFATE SYNTHESIS UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. 2016-03-03 US disclosed
EP-2406270-B1 METHOD FOR MANUFACTURING 4-FLUORO-4-DESOXY-ALPHA-D-GLUCOPYRANOSIDES SANOFI SA (FR) 2013-04-17 EP disclosed
US-20120270819-A1 USE OF COMPOUNDS WITH SGLT-1/SGLT-2 INHIBITOR ACTIVITY FOR PRODUCING MEDICAMENTS FOR TREATMENT OF BONE DISEASE SANOFI (FR) 2012-10-25 US disclosed
EP-2482823-A2 USE OF COMPOUNDS WITH SGLT-1/SGLT-2 INHIBITOR ACTIVITY FOR PRODUCING MEDICAMENTS FOR TREATMENT OF BONE DISEASES SANOFI (FR) 2012-08-08 EP disclosed
US-20120142560-A1 HEPARAN SULFATE SYNTHESIS UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2012-06-07 US disclosed
WO-2011039338-A2 USE OF COMPOUNDS WITH SGLT-1/SGLT-2 INHIBITOR ACTIVITY FOR PRODUCING MEDICAMENTS FOR TREATMENT OF BONE DISEASES SANOFI-AVENTIS (FR) 2011-04-07 WO disclosed
US-20100267940-A1 Method for Producing 4-Deoxy-4-Fluoro-D-Glucose Derivative CENTRAL GLASS COMPANY, LIMITED (JP) 2010-10-21 US disclosed
WO-2004052902-A1 NOVEL AROMATIC FLUOROGLYCOSIDE DERIVATIVES, PHARMACEUTICAL PRODUCTS CONTAINING SAID COMPOUNDS AND THE USE THEREOF AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2004-06-24 WO disclosed
WO-2004052903-A1 NOVEL FLUOROGLYCOSIDE HETEROCYCLIC DERIVATIVES, PHARMACEUTICAL PRODUCTS CONTAINING SAID COMPOUNDS AND THE USE THEREOF AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2004-06-24 WO 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-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
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

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20100267940-A1 Method for Producing 4-Deoxy-4-Fluoro-D-Glucose Derivative SLC5A2, PFKFB3, PFKFB2 LGALS3 160/4885LGALS4 120/4885LGALS9 86/4885
US-10174132-B2 Heparan sulfate synthesis HPSE, STT3B, DDOST LGALS3 250/4885LGALS4 169/4885LGALS9 258/4885
US-20160060365-A1 HEPARAN SULFATE SYNTHESIS HPSE, STT3B, DDOST LGALS3 250/4885LGALS4 169/4885LGALS9 258/4885
US-20120270819-A1 USE OF COMPOUNDS WITH SGLT-1/SGLT-2 INHIBITOR ACTIVITY FOR PRODUCING MEDICAMENTS FOR TREATMENT OF BONE DISEASE SLC5A1, SLC5A2, SOST LGALS3 240/4885LGALS4 199/4885LGALS9 272/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.