Miglustat

Miglustat

SCHEMBL7908066

CCCCN1CC(O)C(O)[C@H](O)C1CO

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

UGCG

The experimentally established mechanism targets of Miglustat. 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
▸ UGCG known ✓ Q16739 3/20 1.00
▸ GBA2 Q9HCG7 18/20 1.00
▸ GBA1 P04062 7/20 1.00
▸ GAA P10253 6/20 1.00
▸ MGAM O43451 2/20 1.00
▸ SI P14410 2/20 1.00
▸ AGL P35573 2/20 1.00
▸ MEN1 O00255 1/20 0.97
▸ LMNA P02545 1/20 0.97
▸ MAPK1 P28482 1/20 0.97
▸ KMT2A Q03164 1/20 0.97

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
Miglustat SCHEMBL19627562 1.00 GBA2 (1.00) GBA2GBA1GAAUGCGMGAM
Miglustat SCHEMBL7911410 1.00 GBA2 (1.00) GBA2GBA1GAAUGCGMGAM
Miglustat SCHEMBL11921340 1.00 GBA2 (1.00) GBA2GBA1GAAUGCGMGAM
Miglustat SCHEMBL13175027 1.00 GBA2 (1.00) GBA2GBA1GAAUGCGMGAM
Miglustat SCHEMBL246893 1.00 GBA2 (1.00) GBA2GBA1GAAUGCGMGAM
Miglustat SCHEMBL23503067 1.00 GBA2 (1.00) GBA2GBA1GAAUGCGMGAM
Miglustat SCHEMBL20577242 1.00 GBA2 (1.00) GBA2GBA1GAAUGCGMGAM
Miglustat SCHEMBL20576705 1.00 GBA2 (1.00) GBA2GBA1GAAUGCGMGAM
Miglustat SCHEMBL20769803 1.00 GBA2 (1.00) GBA2GBA1GAAUGCGMGAM
Miglustat SCHEMBL19627563 1.00 GBA2 (1.00) GBA2GBA1GAAUGCGMGAM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230270826-A1 ANTIVIRAL USE OF LIRAGLUTIDE AND GEFITINIB DELTA 4 GMBH (AT) 2023-08-31 — — US disclosed
EP-3957320-B1 AUGMENTED ACID ALPHA-GLUCOSIDASE FOR THE TREATMENT OF POMPE DISEASE AMICUS THERAPEUTICS INC (US) 2023-08-23 — — EP disclosed
US-20230220320-A1 Method For Capturing And Purification Of Biologics AMICUS THERAPEUTICS, INC. (US) 2023-07-13 — — US disclosed
US-20220184185-A1 MRNA BASED ENZYME REPLACEMENT THERAPY COMBINED WITH A PHARMACOLOGICAL CHAPERONE FOR THE TREATMENT OF LYSOSOMAL STORAGE DISORDERS MODERNATX, INC. 2022-06-16 — — US disclosed
EP-3957320-A1 AUGMENTED ACID ALPHA-GLUCOSIDASE FOR THE TREATMENT OF POMPE DISEASE Amicus Therapeutics, Inc. (US) 2022-02-23 — — EP disclosed
WO-2022023533-A2 ANTIVIRAL USE OF LIRAGLUTIDE AND GEFITINIB DELTA 4 GMBH (AT) 2022-02-03 — — WO disclosed
EP-3397273-B1 AUGMENTED ACID ALPHA-GLUCOSIDASE FOR THE TREATMENT OF POMPE DISEASE AMICUS THERAPEUTICS INC (US) 2021-05-19 — — EP disclosed
US-10857212-B2 Augmented acid alpha-glucosidase for the treatment of Pompe disease AMICUS THERAPEUTICS, INC. (US) 2020-12-08 — — US disclosed
US-10227577-B2 Method for selection of high M6P recombinant proteins AMICUS THERAPEUTICS, INC. (US) 2019-03-12 — — US disclosed
US-20170335301-A1 Method for Selection of High M6P Recombinant Proteins WILMINGTON TRUST, NATIONAL ASSOCIATION 2017-11-23 — — US disclosed
WO-2017173059-A1 METHOD FOR SELECTION OF HIGH M6P RECOMBINANT PROTEINS AMICUS THERAPEUTICS, INC. (US) 2017-10-05 — — WO disclosed
WO-2017117407-A1 AUGMENTED ACID ALPHA-GLUCOSIDASE FOR THE TREATMENT OF POMPE DISEASE AMICUS THERAPEUTICS, INC. (US) 2017-07-06 — — WO disclosed
US-20170189497-A1 Augmented Acid Alpha-Glucosidase For The Treatment Of Pompe Disease WILMINGTON TRUST, NATIONAL ASSOCIATION 2017-07-06 — — US disclosed
EP-0624652-B1 Process for producing N-substituted polyhydroxy nitrogen-containing heterocycles MONSANTO CO (US) 2001-10-10 — — EP disclosed
EP-1132370-A2 Process for producing n-substituted polyhydroxy nitrogen-containing heterocyles MONSANTO COMPANY (US) 2001-09-12 — — EP disclosed
US-5401645-A Process for producing n-substituted polyhydroxy nitrogen-containing heterocycles utilizing acetobacteraceae and corynebacterium MONSANTO COMPANY (US) 1995-03-28 — — US disclosed
EP-0624652-A1 Process for producing N-substituted polyhydroxy nitrogen-containing heterocycles MONSANTO COMPANY (US) 1994-11-17 — — EP 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 (6 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-20170189497-A1 Augmented Acid Alpha-Glucosidase For The Treatment Of Pompe Disease GAA, MAN2B1, MANBA UGCG 40/4885GBA2 19/4885GBA1 9/4885
US-10227577-B2 Method for selection of high M6P recombinant proteins M6PR, MAN2B1, MTAP UGCG 393/4885GBA2 80/4885GBA1 29/4885
US-20170335301-A1 Method for Selection of High M6P Recombinant Proteins M6PR, MAN2B1, MTAP UGCG 393/4885GBA2 80/4885GBA1 29/4885
US-20230270826-A1 ANTIVIRAL USE OF LIRAGLUTIDE AND GEFITINIB GLP1R, SLC5A1, DPP4 UGCG 2269/4885GBA2 3435/4885GBA1 1375/4885
US-10857212-B2 Augmented acid alpha-glucosidase for the treatment of Pompe disease GAA, MAN2B1, MANBA UGCG 40/4885GBA2 19/4885GBA1 9/4885
US-20220184185-A1 MRNA BASED ENZYME REPLACEMENT THERAPY COMBINED WITH A PHARMACOLOGICAL CHAPERONE FOR THE TREATMENT OF LYSOSOMAL STORAGE DISORDERS GAA, GBA1, GBA2 UGCG 14/4885GBA2 3/4885GBA1 2/4885

“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.

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