SCHEMBL366469

SCHEMBL366469

C=CCN1C[C@H](O)[C@@H](O)[C@H](O)[C@H]1CO

nearest known ligand 0.59

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
GAA P10253 9/20 0.59
MGAM O43451 6/20 0.59
SI P14410 3/20 0.59
GBA1 P04062 2/20 0.59
TDP1 Q9NUW8 1/20 0.59
LCT P09848 1/20 0.59
GBA2 Q9HCG7 8/20 0.53
UGCG Q16739 3/20 0.53
AGL P35573 3/20 0.53
MEN1 O00255 1/20 0.51
LMNA P02545 1/20 0.51
MAPK1 P28482 1/20 0.51
KMT2A Q03164 1/20 0.51

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
SCHEMBL9426822 1.00 GAA (0.59) GAAMGAMSIGBA1TDP1
SCHEMBL466824 1.00 GAA (0.59) GAAMGAMSIGBA1TDP1
SCHEMBL2265507 0.82 GAA (0.66) GAAMGAMSIGBA1TDP1
SCHEMBL18709118 0.81 GAA (0.59) GAAMGAMSIGBA1TDP1
SCHEMBL17128703 0.79 GAA (0.66) GAAMGAMSIGBA1TDP1
SCHEMBL26679472 0.78 GAA (0.70) GAAMGAMSIGBA1TDP1
SCHEMBL2270637 0.78 GAA (0.70) GAAMGAMSIGBA1TDP1
Methane SCHEMBL9426826 0.77 GAA (0.36) GAAMGAMSIGBA1TDP1
SCHEMBL2274019 0.76 GAA (0.68) GAAMGAMSIGBA1TDP1
SCHEMBL23996577 0.76 GAA (0.49) GAAMGAMSIGBA1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5411970-A Method of inhibiting lentivirus G. D. SEARLE & CO. (US) 1995-05-02 US claimed
EP-0445098-A2 Deoxynojirimycin derivatives as antiviral agents G.D. SEARLE & COMPANY (US) 1991-09-04 EP claimed
US-4957926-A ALKYLIMINO-DIDEOXY-GLUCITOL COMPOUND MONSANTO COMPANY (US) 1990-09-18 US claimed
EP-2023927-B1 DEOXYNOJIRIMYCIN AND D-ARABINITOL ANALOGS AND METHODS OF USING UNITED THERAPEUTICS CORP (US) 2015-02-25 EP disclosed
US-8097728-B2 Iminosugar compounds with antiflavirus activity PHILADELPHIA HEALTH & EDUCATION CORPORATION (US) 2012-01-17 US disclosed
US-7612093-B2 Compositions of treating hepatitis virus infections with N-substituted-1,5-dideoxy-1,5-imino-D-glucitol compounds in combination therapy UNITED THERAPEUTICS CORPORATION (US) 2009-11-03 US disclosed
US-20090042268-A1 IMINOSUGAR COMPOUNDS WITH ANTIFLAVIRUS ACTIVITY NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2009-02-12 US disclosed
EP-1658846-B1 N-(8,8,8-trifluorooctyl)-1,5-dideoxy-1,5-imino-D-glucitol for treating hepatitis virus infections UNITED THERAPEUTICS CORP (US) 2008-07-30 EP disclosed
EP-1061922-B9 USE OF N-SUBSTITUTED-1,5-DIDEOXY-1,5-IMINO-D-GLUCITOL COMPOUNDS FOR TREATING HEPATITIS VIRUS INFECTIONS UNITED THERAPEUTICS CORP (US) 2007-03-07 EP disclosed
US-20060264468-A1 Use of substituted-1, 5-dideoxy-1, 5-imino-D-glucitol compounds for treating hepatitis virus infections UNITED THERAPEUTICS CORPORATION 2006-11-23 US disclosed
EP-1714676-A2 Use of N-substituted-1,5-dideoxy-1,5-imino-D-glucitol compounds for treating hepatitis virus infections G.D. Searle LLC. (US) 2006-10-25 EP disclosed
EP-1061922-A1 USE OF $i(N)-SUBSTITUTED-1,5-DIDEOXY-1,5-IMINO-D-GLUCITOL COMPOUNDS FOR TREATING HEPATITIS VIRUS INFECTIONS G.D. SEARLE & CO. (US) 2000-12-27 EP disclosed
EP-1030839-A1 USE OF ALKYLATED IMINOSUGARS TO TREAT MULTIDRUG RESISTANCE G.D. SEARLE & CO. (US) 2000-08-30 EP disclosed
WO-1999040916-A1 USE OF N-SUBSTITUTED-1,5-DIDEOXY-1,5-IMINO-D-GLUCITOL COMPOUNDS FOR TREATING HEPATITIS VIRUS INFECTIONS G.D. SEARLE & CO. (US) 1999-08-19 WO disclosed
WO-1999024401-A1 USE OF ALKYLATED IMINOSUGARS TO TREAT MULTIDRUG RESISTANCE G.D. SEARLE & CO. (US) 1999-05-20 WO disclosed
US-5151519-A PROCESS FOR THE PREPARATION OF 1,5-(ALKYLIMINO)-1,5-DIDEOXY-D-GLUCITOL AND DERIVATIVES THEREOF G. D. SEARLE & CO. (US) 1992-09-29 US disclosed
US-5151519-A PROCESS FOR THE PREPARATION OF 1,5-(ALKYLIMINO)-1,5-DIDEOXY-D-GLUCITOL AND DERIVATIVES THEREOF G. D. SEARLE & CO. (US) 1992-09-29 US disclosed
WO-1991017145-A1 PROCESS FOR PREPARATION OF 1,5-(ALKYLIMINO)-1,5-DIDEOXY-D-GLUCITOL AND DERIVATIVES THEREOF G.D. SEARLE & CO. (US) 1991-11-14 WO disclosed
WO-1991017145-A1 PROCESS FOR PREPARATION OF 1,5-(ALKYLIMINO)-1,5-DIDEOXY-D-GLUCITOL AND DERIVATIVES THEREOF G.D. SEARLE & CO. (US) 1991-11-14 WO disclosed
WO-1991017145-A1 PROCESS FOR PREPARATION OF 1,5-(ALKYLIMINO)-1,5-DIDEOXY-D-GLUCITOL AND DERIVATIVES THEREOF G.D. SEARLE & CO. (US) 1991-11-14 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 (2 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-20060264468-A1 Use of substituted-1, 5-dideoxy-1, 5-imino-D-glucitol compounds for treating hepatitis virus infections IMPDH1, HAVCR2, DERA GAA 429/4885MGAM 60/4885SI 151/4885
US-20090042268-A1 IMINOSUGAR COMPOUNDS WITH ANTIFLAVIRUS ACTIVITY INSRR, RNASEL, AGL GAA 1145/4885MGAM 73/4885SI 203/4885

“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.