SCHEMBL1088846

SCHEMBL1088846

CC(=O)N[C@H](CN1CCCC1)[C@H](O)c1ccc2c(c1)OCCO2

nearest known ligand 0.71

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
UGCG Q16739 15/20 0.71
PTGS1 P23219 2/20 0.71
HTR1A P08908 1/20 0.71
OPRM1 P35372 1/20 0.71
HTT P42858 1/20 0.44
KDM4E B2RXH2 1/20 0.43
ALDH1A1 P00352 1/20 0.43
MCL1 Q07820 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
AOC3 Q16853 1/20 0.43
PTGS2 P35354 1/20 0.43
HPGD P15428 1/20 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
SCHEMBL1088358 1.00 UGCG (0.71) UGCGPTGS1HTR1AOPRM1HTT
SCHEMBL13081778 1.00 UGCG (0.71) UGCGPTGS1HTR1AOPRM1HTT
SCHEMBL14069053 1.00 UGCG (0.71) UGCGPTGS1HTR1AOPRM1HTT
SCHEMBL13098312 0.93 UGCG (0.63) UGCGPTGS1HTR1AOPRM1KDM4E
SCHEMBL19354952 0.92 UGCG (0.62) UGCGPTGS1HTR1AOPRM1HTT
SCHEMBL23731734 0.91 UGCG (0.69) UGCGPTGS1HTR1AOPRM1HTT
SCHEMBL22463696 0.90 UGCG (0.70) UGCGPTGS1HTR1AOPRM1KDM4E
SCHEMBL22463695 0.90 UGCG (0.70) UGCGPTGS1HTR1AOPRM1KDM4E
SCHEMBL7993471 0.90 UGCG (0.58) UGCGPTGS1HTR1AOPRM1HTT
SCHEMBL23731735 0.89 UGCG (0.69) UGCGPTGS1HTR1AOPRM1HTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11697644-B2 Process for synthesis of eliglustat and intermediate compounds thereof ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. (CN) 2023-07-11 US disclosed
US-11697644-B2 Process for synthesis of eliglustat and intermediate compounds thereof ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. (CN) 2023-07-11 US disclosed
US-11358932-B2 N-(1-hydroxy-3-(pyrrolidinyl)propan-2-yl)pyrrolidine-3-carboxamide derivatives as glucosylceramide synthase inhibitors BIOMARIN PHARMACEUTICAL INC. (US) 2022-06-14 US disclosed
EP-3611171-A1 METHOD FOR SYNTHESIS OF ELIGLUSTAT AND INTERMEDIATE COMPOUNDS THEREOF Zhejiang Ausun Pharmaceutical Co., Ltd. (CN) 2020-02-19 EP disclosed
US-20200031808-A1 PROCESS FOR SYNTHESIS OF ELIGLUSTAT AND INTERMEDIATE COMPOUNDS THEREOF ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. (CN) 2020-01-30 US disclosed
US-20190276398-A1 N-(1-HYDROXY-3-(PYRROLIDINYL)PROPAN-2-YL)PYRROLIDINE-3-CARBOXAMIDE DERIVATIVES AS GLUCOSYLCERAMIDE SYNTHASE INHIBITORS BIOMARIN PHARM INC (US) 2019-09-12 US disclosed
US-10239832-B2 N-(1-hydroxy-3-(pyrrolidinyl)propan-2-yl)pyrrolidine-3-carboxamide derivatives as glucosylceramide synthase inhibitors BIOMARIN PHARMACEUTICAL INC. (US) 2019-03-26 US disclosed
US-10227323-B2 Glucosylceramide synthase inhibitors for the treatment of diseases BIOMARIN PHARMACEUTICAL INC. (US) 2019-03-12 US disclosed
US-9988364-B1 Process for synthesis of Eliglustat and intermediate compounds thereof ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. (CN) 2018-06-05 US disclosed
US-9988364-B1 Process for synthesis of Eliglustat and intermediate compounds thereof ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. (CN) 2018-06-05 US disclosed
US-20100048642-A1 METHODS FOR TREATING COGNITIVE DISORDERS ALLERGAN, INC. (US) 2010-02-25 US disclosed
US-20090318499-A1 COMPOUNDS HAVING ANALGESIC AND/OR IMMUNOSTIMULANT ACTIVITY ALLERGAN, INC. 2009-12-24 US disclosed
US-20090281085-A1 3-(4-FLUOROPHENYL)-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES AND RELATED COMPOUNDS HAVING ANALGESIC ACTIVITY ALLERGAN, INC. 2009-11-12 US disclosed
US-20090088433-A1 METHODS OF USING AS ANALGESICS 1-BENZYL-1-HYDROXY-2,3-DIAMINO-PROPYL AMINES, 3-BENZYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES AND RELATED COMPOUNDS ALLERGAN, INC. 2009-04-02 US disclosed
US-20090036436-A1 3-ARYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES, 3-HETEROARYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES AND RELATED COMPOUNDS HAVING ANALGESIC AND/OR IMMUNO STIMULANT ACTIVITY ALLERGAN, INC. 2009-02-05 US disclosed
US-20080312236-A1 3-Heteroaryl-3-Hydroxy-2-Amino-Propyl Amines And Related Compounds Having Analgesic And/Or Immuno Stimlant Activity EXONHIT THERAPEUTICS SA (FR) 2008-12-18 US disclosed
WO-2008109286-A1 METHODS FOR TREATING COGNITIVE DISORDERS USING 1-ARYL-1-HYDROXY-2,3-DIAMINO-PROPYL AMINES, 1-HETEROARYL-1-HYDROXY-2,3-DIAMINO-PROPYL AMINES AND RELATED COMPOUNDS ALLERGAN, INC. (US) 2008-09-12 WO disclosed
US-7265228-B2 Synthesis of UDP-glucose: N-acylsphingosine glucosyltransferase inhibitors GENZYME CORPORATION (US) 2007-09-04 US disclosed
US-20070203223-A1 Synthesis of UDP-glucose: N-acylsphingosine glucosyltransferase inhibitors THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2007-08-30 US disclosed
US-7196205-B2 Synthesis of amino ceramide-like compounds; for treating Tay-Sachs, Gaucher's or Fabry's disease; amenable to large scale preparations THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2007-03-27 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 (13 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-20080312236-A1 3-Heteroaryl-3-Hydroxy-2-Amino-Propyl Amines And Related Compounds Having Analgesic And/Or Immuno Stimlant Activity OPRL1, OPRM1, MRGPRX2 UGCG 2783/4885PTGS1 85/4885HTR1A 188/4885
US-20090088433-A1 METHODS OF USING AS ANALGESICS 1-BENZYL-1-HYDROXY-2,3-DIAMINO-PROPYL AMINES, 3-BENZYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES AND RELATED COMPOUNDS OPRL1, OPRK1, AADAT UGCG 4208/4885PTGS1 56/4885HTR1A 81/4885
US-20090036436-A1 3-ARYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES, 3-HETEROARYL-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES AND RELATED COMPOUNDS HAVING ANALGESIC AND/OR IMMUNO STIMULANT ACTIVITY OPRL1, HCAR2, OPRM1 UGCG 4112/4885PTGS1 168/4885HTR1A 88/4885
US-20090281085-A1 3-(4-FLUOROPHENYL)-3-HYDROXY-2-AMINO-PROPIONIC ACID AMIDES AND RELATED COMPOUNDS HAVING ANALGESIC ACTIVITY OPRL1, OPRK1, OPRM1 UGCG 3951/4885PTGS1 17/4885HTR1A 271/4885
US-11697644-B2 Process for synthesis of eliglustat and intermediate compounds thereof EPOR, FGFR1, ABL1 UGCG 555/4885PTGS1 1241/4885HTR1A 3787/4885
US-20090318499-A1 COMPOUNDS HAVING ANALGESIC AND/OR IMMUNOSTIMULANT ACTIVITY OPRK1, OPRM1, OPRL1 UGCG 3478/4885PTGS1 64/4885HTR1A 1217/4885
US-11358932-B2 N-(1-hydroxy-3-(pyrrolidinyl)propan-2-yl)pyrrolidine-3-carboxamide derivatives as glucosylceramide synthase inhibitors GBA1, UGCG, GBA2 UGCG 2/4885PTGS1 128/4885HTR1A 3038/4885
US-20190276398-A1 N-(1-HYDROXY-3-(PYRROLIDINYL)PROPAN-2-YL)PYRROLIDINE-3-CARBOXAMIDE DERIVATIVES AS GLUCOSYLCERAMIDE SYNTHASE INHIBITORS GBA1, UGCG, GBA2 UGCG 2/4885PTGS1 128/4885HTR1A 3038/4885
US-20070203223-A1 Synthesis of UDP-glucose: N-acylsphingosine glucosyltransferase inhibitors UGCG, UGGT1, DPAGT1 UGCG 1/4885PTGS1 2317/4885HTR1A 3504/4885
US-20100048642-A1 METHODS FOR TREATING COGNITIVE DISORDERS CHAT, SLC18A3, SLC18A2 UGCG 556/4885PTGS1 2164/4885HTR1A 118/4885
US-10227323-B2 Glucosylceramide synthase inhibitors for the treatment of diseases GBA1, UGCG, GBA2 UGCG 2/4885PTGS1 290/4885HTR1A 4274/4885
US-20200031808-A1 PROCESS FOR SYNTHESIS OF ELIGLUSTAT AND INTERMEDIATE COMPOUNDS THEREOF COASY, ELL, CYP3A4 UGCG 442/4885PTGS1 970/4885HTR1A 4060/4885
US-10239832-B2 N-(1-hydroxy-3-(pyrrolidinyl)propan-2-yl)pyrrolidine-3-carboxamide derivatives as glucosylceramide synthase inhibitors GBA1, UGCG, GBA2 UGCG 2/4885PTGS1 130/4885HTR1A 2749/4885

“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.