Dextrose

Dextrose

SCHEMBL6038162

O=P(O)(O)O.OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Dextrose. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
LGALS1 P09382 2/20 0.48
LGALS3 P17931 2/20 0.48
LGALS9 O00182 1/20 0.48
LGALS8 O00214 1/20 0.48
CA12 O43570 3/20 0.43
CA1 P00915 3/20 0.43
CA2 P00918 3/20 0.43
CA9 Q16790 3/20 0.43
FBP1 P09467 1/20 0.42
PYGB P11216 7/20 0.42
GAA P10253 1/20 0.42

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
Beta-D-Glucose SCHEMBL361597 1.00 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
B-D-Galactose SCHEMBL361799 1.00 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
B-D-Galactose SCHEMBL16429773 1.00 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
Dextrose SCHEMBL7651668 1.00 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
D-Mannose SCHEMBL1772795 1.00 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
D-Galactose SCHEMBL17593535 1.00 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
B-D-Galactose SCHEMBL361340 1.00 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
B-D-Galactose SCHEMBL361515 1.00 LGALS1 (0.48) LGALS1LGALS3LGALS9LGALS8CA12
B-D-Galactose SCHEMBL9847381 0.98 LGALS1 (0.47) LGALS1LGALS3LGALS9LGALS8CA12
Ribose (Furanose) SCHEMBL27896040 0.98 LGALS1 (0.45) LGALS1LGALS3LGALS9LGALS8CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101610798-A Drug releasing coatings for medical devices LUTONIX INC (US) 2009-12-23 CN claimed
US-20230165840-A1 TREATMENT OF ASTHMA AND CHRONIC OBSTRUCTIVE PULMONARY DISEASE WITH ANTI-PROLIFERATE AND ANTI-INFLAMMATORY DRUGS LUTONIX, INC. (US) 2023-06-01 US disclosed
US-11534430-B2 Treatment of asthma and chronic obstructive pulmonary disease with anti-proliferate and anti-inflammatory drugs LUTONIX, INC. (US) 2022-12-27 US disclosed
CN-109328297-A Container assemblies and the preparation method of sample for using the container assemblies 株式会社岛津制作所 2019-02-12 CN disclosed
EP-3191598-A1 PROCESS FOR THE ENZYMATIC PREPARATION OF A PRODUCT GLUCOSIDE AND OF A CO-PRODUCT FROM AN EDUCT GLUCOSIDE Pfeifer & Langen GmbH & Co. KG (DE) 2017-07-19 EP disclosed
WO-2016038142-A1 PROCESS FOR THE ENZYMATIC PREPARATION OF A PRODUCT GLUCOSIDE AND OF A CO-PRODUCT FROM AN EDUCT GLUCOSIDE Pfeifer & Langen GmbH & Co. KG (DE) 2016-03-17 WO disclosed
CN-101610798-B Drug releasing coatings for medical devices LUTONIX INC 2013-07-17 CN disclosed
CN-101610798-A Drug releasing coatings for medical devices LUTONIX INC (US) 2009-12-23 CN disclosed
US-7102023-B2 Protecting groups useful in the synthesis of polysaccharides, natural products, and combinatorial libraries MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2006-09-05 US disclosed
US-20040220389-A1 Protecting groups useful in the synthesis of polysaccharides, natural products, and combinatorial libraries NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2004-11-04 US 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 (1 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-20040220389-A1 Protecting groups useful in the synthesis of polysaccharides, natural products, and combinatorial libraries FUT5, FUT6, UGCG LGALS1 87/4885LGALS3 53/4885LGALS9 79/4885

“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.