Deoxyfuconojirimycin

Deoxyfuconojirimycin

SCHEMBL2435560

C[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
FUCA1 P04066 5/20 1.00
FUCA2 Q9BTY2 1/20 1.00
GLB1 P16278 1/20 0.58
GBA1 P04062 5/20 0.54
GLA P06280 1/20 0.48
GAA P10253 1/20 0.48
GANAB Q14697 1/20 0.46
MAN2B1 O00754 1/20 0.46
MAN2B2 Q9Y2E5 1/20 0.46

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
Deoxyfuconojirimycin SCHEMBL15686574 1.00 FUCA1 (1.00) FUCA1FUCA2GLB1GBA1GLA
Deoxyfuconojirimycin SCHEMBL13876082 1.00 FUCA1 (1.00) FUCA1FUCA2GLB1GBA1GLA
Deoxyfuconojirimycin SCHEMBL4378188 1.00 FUCA1 (1.00) FUCA1FUCA2GLB1GBA1GLA
Deoxyfuconojirimycin SCHEMBL1867289 1.00 FUCA1 (1.00) FUCA1FUCA2GLB1GBA1GLA
Deoxyfuconojirimycin SCHEMBL12581516 1.00 FUCA1 (1.00) FUCA1FUCA2GLB1GBA1GLA
Deoxyfuconojirimycin SCHEMBL9999893 1.00 FUCA1 (1.00) FUCA1FUCA2GLB1GBA1GLA
Deoxyfuconojirimycin SCHEMBL13328524 1.00 FUCA1 (1.00) FUCA1FUCA2GLB1GBA1GLA
Deoxyfuconojirimycin SCHEMBL2436650 1.00 FUCA1 (1.00) FUCA1FUCA2GLB1GBA1GLA
Deoxyfuconojirimycin SCHEMBL15691930 1.00 FUCA1 (1.00) FUCA1FUCA2GLB1GBA1GLA
Deoxyfuconojirimycin SCHEMBL13876087 1.00 FUCA1 (1.00) FUCA1FUCA2GLB1GBA1GLA

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-10842784-B2 Treatment of energy utilization disease VIDA PHARMA LIMITED (GB) 2020-11-24 US disclosed
US-20110237538-A1 TREATMENT OF LYSOSOMAL STORAGE DISORDERS AND OTHER PROTEOSTATIC DISEASES SUMMIT CORPORATION PLC (GB) 2011-09-29 US disclosed
US-20110015226-A1 Treatment of Energy Utilization Disease SUMMIT CORPORATION PLC (GB) 2011-01-20 US disclosed
US-20090117083-A1 IMMUNOMODULATORY ALKALOIDS M N L PHARMA LIMITED (UK) 2009-05-07 US disclosed
US-20090047306-A1 ADJUVANT COMPOSITIONS M N L PHARMA LIMITED (UK) 2009-02-19 US disclosed
US-6831176-B2 Reacting a ketoaldonic acid methyl ester of the sugar with the protected hydroxyl groups with a an alkylamine or hydroxyalamine salt in an organic solvent with a tert-amine to react with acid generated to produce oxime methyl ester BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY 2004-12-14 US disclosed
US-6740780-B2 L-XYLO-5-HEXULOSONIC ACID HYDRAZIDE OXIME BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY 2004-05-25 US disclosed
US-6683185-B2 FROM HYDROXYL-PROTECTED OXIME INTERMEDIATES, INCLUDES FORMATION OF A LACTAM WHICH IS REDUCED TO THE HEXITOL; CHEMICAL INTERMEDIATES TO D-DIDEOXYGALACTO-NOJIRIMYCINS BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY 2004-01-27 US disclosed
US-6653480-B2 Generating aldonic-5-oxime ethyl ester with protected hydroxyls; obtain keto-methyl sugar ester, incubate with hydroxylamine hydrochloride, separate oxime methyl ester from mixture BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY 2003-11-25 US disclosed
US-6653482-B2 The ketoaldonic acid methyl ester is converted into the oxime which is then reduced to the amine which cyclizes to give the lactam which is then reduced to the imino sugar by borane or a metal hydride BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY 2003-11-25 US disclosed
EP-0576592-B1 OLIGOSACCHARIDE ENZYME SUBSTRATES AND INHIBITORS: METHODS AND COMPOSITIONS SCRIPPS RESEARCH INST (US) 2000-05-31 EP disclosed
US-5759823-A MIXING IN AQUEOUS MEDIUM ACTIVATED DONOR MONOSACCHARIDE WITH ACCEPTOR SACCHARIDE IN PRESENCE OF GLYCOSYLTRANSFERASE, MAINTAINING TO GLYCOSYLATE ACCEPTOR SACCHARIDE SCRIPPS RESEARCH INSTITUTE (US) 1998-06-02 US disclosed
US-5596005-A GLYCOSIDASE INHIBITORS THE SCRIPPS RESEARCH INSTITUTE (US) 1997-01-21 US disclosed
US-5593887-A Oligosaccharide enzyme substrates and inhibitors: methods and compositions THE SCRIPPS RESEARCH INSTITUTE (US) 1997-01-14 US disclosed
EP-0576592-A4 OLIGOSACCHARIDE ENZYME SUBSTRATES AND INHIBITORS: METHODS AND COMPOSITIONS SCRIPPS RESEARCH INST (US) 1996-01-24 EP disclosed
US-5461143-A Oligosaccharide enzyme substrates and inhibitors: methods and compositions THE SCRIPPS RESEARCH INSTITUTE (US) 1995-10-24 US disclosed
EP-0576592-A1 OLIGOSACCHARIDE ENZYME SUBSTRATES AND INHIBITORS: METHODS AND COMPOSITIONS THE SCRIPPS RESEARCH INSTITUTE (US) 1994-01-05 EP disclosed
US-5276120-A Reductively cyclizing an azido-substituted alpha-ketose phosphate; palladium catalyzed THE SCRIPPS RESEARCH INSTITUTE (US) 1994-01-04 US disclosed
WO-1992021657-A1 OMEGA-DEOXY-AZASUGARS THE SCRIPPS RESEARCH INSTITUTE (US) 1992-12-10 WO disclosed
WO-1992016640-A1 OLIGOSACCHARIDE ENZYME SUBSTRATES AND INHIBITORS: METHODS AND COMPOSITIONS THE SCRIPPS RESEARCH INSTITUTE (US) 1992-10-01 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 (5 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-20110237538-A1 TREATMENT OF LYSOSOMAL STORAGE DISORDERS AND OTHER PROTEOSTATIC DISEASES GAA, MAN2B1, GBA1 FUCA1 17/4885FUCA2 18/4885GLB1 33/4885
US-20090117083-A1 IMMUNOMODULATORY ALKALOIDS IL2, IL2RA, IDO2 FUCA1 4102/4885FUCA2 1989/4885GLB1 4128/4885
US-10842784-B2 Treatment of energy utilization disease IRS1, SLC2A1, INSR FUCA1 1506/4885FUCA2 1138/4885GLB1 1210/4885
US-20110015226-A1 Treatment of Energy Utilization Disease IRS1, SLC2A1, INSR FUCA1 1506/4885FUCA2 1138/4885GLB1 1210/4885
US-20090047306-A1 ADJUVANT COMPOSITIONS CD4, LY96, CD209 FUCA1 107/4885FUCA2 83/4885GLB1 2487/4885

“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.