SCHEMBL723342

SCHEMBL723342

CCCCCCCCCC(=O)N[C@H](CN1CCOCC1)[C@H](O)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
UGCG Q16739 9/20 1.00
KMT2A Q03164 3/20 1.00
MEN1 O00255 2/20 1.00
TP53 P04637 1/20 1.00
CYP3A4 P08684 1/20 1.00
CYP2D6 P10635 1/20 1.00
CYP2C9 P11712 1/20 1.00
NFKB1 P19838 1/20 1.00
MAPK1 P28482 1/20 1.00
CYP2C19 P33261 1/20 1.00
HIF1A Q16665 1/20 1.00
MAPT P10636 1/20 1.00
MTOR P42345 1/20 1.00
GMNN O75496 1/20 0.98
LMNA P02545 1/20 0.98
BLM P54132 1/20 0.98
PMP22 Q01453 1/20 0.98
SMN1; SMN2 Q16637 1/20 0.98
NPSR1 Q6W5P4 1/20 0.98
HTR1A P08908 1/20 0.62

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
SCHEMBL363373 1.00 UGCG (1.00) UGCGKMT2AMEN1TP53CYP3A4
SCHEMBL840939 1.00 UGCG (1.00) UGCGKMT2AMEN1TP53CYP3A4
SCHEMBL14304968 1.00 UGCG (1.00) UGCGKMT2AMEN1TP53CYP3A4
SCHEMBL12000798 1.00 UGCG (1.00) UGCGKMT2AMEN1TP53CYP3A4
SCHEMBL5452846 1.00 UGCG (1.00) UGCGKMT2AMEN1TP53CYP3A4
SCHEMBL295573 1.00 UGCG (1.00) UGCGKMT2AMEN1TP53CYP3A4
SCHEMBL23845860 1.00 UGCG (1.00) UGCGKMT2AMEN1TP53CYP3A4
SCHEMBL137622 1.00 UGCG (1.00) UGCGKMT2AMEN1TP53CYP3A4
SCHEMBL13460643 1.00 UGCG (1.00) UGCGKMT2AMEN1TP53CYP3A4
SCHEMBL13460354 1.00 UGCG (1.00) UGCGKMT2AMEN1TP53CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090202439-A1 Methods for treatment of angiogenesis THE JOHNS HOPKINS UNIVERSITY (US) 2009-08-13 US claimed
US-20230165803-A1 BIOPOLYMER-ENCAPSULATED GLYCOSYLTRANSFERASE INHIBITOR COMPOSITIONS AND METHODS FOR TREATING DIABETES AND CARDIAC INDICATIONS UNIV JOHNS HOPKINS (US) 2023-06-01 US disclosed
US-20210386678-A1 BIOPOLYMER-ENCAPSULATED GLYCOSYL TRANSFERASE INHIBITOR COMPOSITIONS AND METHODS FOR TREATING DIABETES AND CARDIAC INDICATIONS UNIV JOHNS HOPKINS (US) 2021-12-16 US disclosed
US-9828349-B2 1-aryl-1-hydroxy-2,3-diamino-propyl amines, 1-heteroaryl-1-hydroxy-2,3-diamino-propyl amines and related compounds having analgesic and/or immuno stimulant activity EXONHIT THERAPEUTICS SA (FR) 2017-11-28 US disclosed
US-9828349-B2 1-aryl-1-hydroxy-2,3-diamino-propyl amines, 1-heteroaryl-1-hydroxy-2,3-diamino-propyl amines and related compounds having analgesic and/or immuno stimulant activity EXONHIT THERAPEUTICS SA (FR) 2017-11-28 US disclosed
US-20170119683-A1 BIOPOLYMER-ENCAPSULATED GLYCOSYL TRANSFERASE INHIBITOR COMPOSITIONS AND METHODS FOR TREATING DIABETES AND CARDIAC INDICATIONS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2017-05-04 US disclosed
US-9399628-B2 1-aryl-1-hydroxy-2,3-diamino-propyl amines, 1-heteroaryl-1-hydroxy-2,3-diamino-propyl amines and related compounds having analgesic and/or immuno stimulant activity ALLERGAN, INC. (US) 2016-07-26 US disclosed
US-9399628-B2 1-aryl-1-hydroxy-2,3-diamino-propyl amines, 1-heteroaryl-1-hydroxy-2,3-diamino-propyl amines and related compounds having analgesic and/or immuno stimulant activity ALLERGAN, INC. (US) 2016-07-26 US disclosed
US-9314466-B2 Methods for treating cognitive disorders using 1-benzyl-1-hydroxy-2,3-diamino-propyl amines, 3-benzyl-3-hydroxy-2-amino-propionic acid amides and related compounds ALLERGAN, INC. (US) 2016-04-19 US disclosed
US-9314466-B2 Methods for treating cognitive disorders using 1-benzyl-1-hydroxy-2,3-diamino-propyl amines, 3-benzyl-3-hydroxy-2-amino-propionic acid amides and related compounds ALLERGAN, INC. (US) 2016-04-19 US disclosed
US-6255336-B1 REDUCING CONCENTRATION OF GLYCOSPHINGOLIPIDS; SYNTHASE INHIBITORS THE REGENTS OF THE UNIVERSITY OF MICHIGAN 2001-07-03 US disclosed
US-6228889-B1 Methods for treatment of conditions associated with lactosylceramide JOHNS HOPKINS UNIVERSITY 2001-05-08 US disclosed
WO-2001004108-A1 AMINO CERAMIDE-LIKE COMPOUNDS AND THERAPEUTIC METHODS OF USE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2001-01-18 WO disclosed
US-6051598-A TREATING A PATIENT HAVING SPHINGOLIPIDOSIS BY REDUCING GLYCOSPHINGOLIPID SYNTHESIS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2000-04-18 US disclosed
US-6040332-A INHIBIT GLUCOSYL CERAMIDE (GLCCER) FORMATION BY INHIBITING THE ENZYME GLCCER SYNTHASE, THEREBY LOWERING THE LEVEL OF GLYCOSPHINGOLIPIDS. THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2000-03-21 US disclosed
US-6030995-A 1-PYRROLIDINO-2-FATTY CARBOXYAMIDO-3-HYDROXY-3-ALKYL- OR ARYLPROPANES; INHIBITORS OF THE GLUCOSYL CERAMIDE SYNTHETASE, THEREBY LOWERING THE LEVEL OF GLYCOSPHINGOLIPIDS; METABOLIC DISORDERS, E.G., TAY-SACHS, GAUCHER'S AND FABRY'S DISEASES, THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2000-02-29 US disclosed
US-5972928-A ADMINISTERING AN ANTIGROWTH AGENT JOHNS HOPKINS UNIVERSITY (US) 1999-10-26 US disclosed
US-5952370-A ADMINISTERING A 1-ALKYL OR ARYL OR ALICYCLIC-2-ALKYLOYLAMINO-3-PYRROLIDINO-1-PROPANOL DERIVATIVE TO TREAT CONDITION OR DISEASES ASSOCIATED WITH GLYCOSYL CERAMIDE FORMATION; ENZYME INHIBITOR THE REGENTS OF UNIVERSITY OF MICHIGAN (US) 1999-09-14 US disclosed
US-5945442-A Amino ceramide-like compounds and therapeutic methods of use THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 1999-08-31 US disclosed
US-5916911-A ANTITUMOR THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 1999-06-29 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 (4 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-20210386678-A1 BIOPOLYMER-ENCAPSULATED GLYCOSYL TRANSFERASE INHIBITOR COMPOSITIONS AND METHODS FOR TREATING DIABETES AND CARDIAC INDICATIONS PNLIP, TNNT2, UGGT1 UGCG 45/4885KMT2A 1822/4885MEN1 3270/4885
US-20090202439-A1 Methods for treatment of angiogenesis B4GALT1, FLT1, FLT4 UGCG 5/4885KMT2A 1679/4885MEN1 4477/4885
US-20230165803-A1 BIOPOLYMER-ENCAPSULATED GLYCOSYLTRANSFERASE INHIBITOR COMPOSITIONS AND METHODS FOR TREATING DIABETES AND CARDIAC INDICATIONS PNLIP, TNNT2, UGGT1 UGCG 38/4885KMT2A 1730/4885MEN1 2578/4885
US-20170119683-A1 BIOPOLYMER-ENCAPSULATED GLYCOSYL TRANSFERASE INHIBITOR COMPOSITIONS AND METHODS FOR TREATING DIABETES AND CARDIAC INDICATIONS OGT, UGGT1, TNNT2 UGCG 48/4885KMT2A 1092/4885MEN1 3423/4885

“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.