SCHEMBL337266

SCHEMBL337266

CCCCCCCCCCCCCCCC(=O)n1nnc2ccccc21

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ASAH1 Q13510 1/20 0.66
KMT2A Q03164 4/20 0.59
HPGD P15428 3/20 0.59
HSD17B10 Q99714 2/20 0.59
MAPT P10636 1/20 0.59
ALOX15 P16050 1/20 0.59
MGAM O43451 2/20 0.56
AMY1A P0DUB6 2/20 0.56
GAA P10253 2/20 0.56
SI P14410 2/20 0.56
MGAM2 Q2M2H8 2/20 0.56
SLC9A1 P19634 5/20 0.55
LMNA P02545 2/20 0.54
CYP4Z1 Q86W10 8/20 0.51
MEN1 O00255 1/20 0.51
ALDH1A1 P00352 1/20 0.51
F2 P00734 1/20 0.50
MITF O75030 1/20 0.49
TSHR P16473 1/20 0.49
MAPK1 P28482 1/20 0.49

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
SCHEMBL535029 1.00 ASAH1 (0.66) ASAH1KMT2AHPGDHSD17B10MAPT
SCHEMBL5793440 1.00 ASAH1 (0.66) ASAH1KMT2AHPGDHSD17B10MAPT
SCHEMBL534899 1.00 ASAH1 (0.66) ASAH1KMT2AHPGDHSD17B10MAPT
SCHEMBL535094 1.00 ASAH1 (0.66) ASAH1KMT2AHPGDHSD17B10MAPT
SCHEMBL18206302 1.00 ASAH1 (0.66) ASAH1KMT2AHPGDHSD17B10MAPT
SCHEMBL534984 1.00 ASAH1 (0.66) ASAH1KMT2AHPGDHSD17B10MAPT
SCHEMBL535030 0.99 ASAH1 (0.64) ASAH1KMT2AHPGDHSD17B10MAPT
SCHEMBL23780256 0.94 KMT2A (0.62) ASAH1KMT2AHPGDHSD17B10MAPT
SCHEMBL18932961 0.92 ASAH1 (0.58) ASAH1KMT2AHPGDHSD17B10MAPT
SCHEMBL534954 0.92 ASAH1 (0.58) ASAH1KMT2AHPGDHSD17B10MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1956000-B1 ACYLATING AGENTS USEFUL FOR ACYLATING PEPTIDES NOVO NORDISK AS (DK) 2016-10-05 EP disclosed
US-8097698-B2 Derivatives of GLP-1 analogs NOVO NORDISK A/S (DK) 2012-01-17 US disclosed
EP-1060191-B1 DERIVATIVES OF GLP-1 ANALOGS NOVO NORDISK AS (DK) 2010-04-28 EP disclosed
US-20090176700-A1 Derivatives Of GLP-1 Analogs NOVO NORDISK A/S (DK) 2009-07-09 US disclosed
EP-1163211-B1 METHOD FOR ACYLATING PEPTIDES AND PROTEINS NOVO NORDISK AS (DK) 2008-09-24 EP disclosed
EP-1956000-A1 Acylating agents useful for acylating peptides Novo Nordisk A/S (DK) 2008-08-13 EP disclosed
US-7235627-B2 Derivatives of GLP-1 analogs NOVO NORDISK A/S (DK) 2007-06-26 US disclosed
US-20060199763-A1 Derivatives of GLP-1 analogs KNUDSEN LISELOTTE B 2006-09-07 US disclosed
EP-0938502-B1 SELECTIVE ACYLATION METHOD NOVO NORDISK AS (DK) 2004-10-06 EP disclosed
EP-1061946-B1 GLP-1 DERIVATIVES WITH HELIX-CONTENT EXCEEDING 25 %, FORMING PARTIALLY STRUCTURED MICELLAR-LIKE AGGREGATES NOVO NORDISK AS (DK) 2004-04-28 EP disclosed
US-20010011071-A1 DERIVATIVES OF GLP-1 ANALOGS KNUDSEN LISELOTTE BJERRE (DK) 2001-08-02 US disclosed
US-6268343-B1 HUMAN GLUCAGON-LIKE PEPTIDE-1; MORE PROTRACTED PROFILE OF ACTION THAN THE PARENT PEPTIDES; TREATING DIABETES AND OBESITY; Liraglutide NOVO NORDISK A/S (DK) 2001-07-31 US disclosed
EP-1061946-A1 GLP-1 DERIVATIVES WITH HELIX-CONTENT EXCEEDING 25 %, FORMING PARTIALLY STRUCTURED MICELLAR-LIKE AGGREGATES NOVO NORDISK A/S (DK) 2000-12-27 EP disclosed
EP-1060191-A1 DERIVATIVES OF GLP-1 ANALOGS NOVO NORDISK A/S (DK) 2000-12-20 EP disclosed
WO-2000055119-A1 METHOD FOR ACYLATING PEPTIDES AND NOVEL ACYLATING AGENTS NOVO NORDISK A/S (DK) 2000-09-21 WO disclosed
WO-1999043706-A1 DERIVATIVES OF GLP-1 ANALOGS NOVO NORDISK A/S (DK) 1999-09-02 WO disclosed
WO-1999043341-A1 GLP-1 DERIVATIVES WITH HELIX-CONTENT EXCEEDING 25 %, FORMING PARTIALLY STRUCTURED MICELLAR-LIKE AGGREGATES NOVO NORDISK A/S (DK) 1999-09-02 WO disclosed
EP-0938502-A1 SELECTIVE ACYLATION METHOD NOVO NORDISK A/S (DK) 1999-09-01 EP disclosed
US-5905140-A ACYLATING INSULIN, INSULIN ANALOGS, AND INSULIN PRECURSORS ON FREE EPSILON-AMINO GROUP OF LYSINE USING ACTIVATED AMIDE WITH ACYL GROUP IN POLAR SOLVENT IN PRESENCE OF BASE NOVO NORDISK A/S, NOVO ALLE (DK) 1999-05-18 US disclosed
WO-1998002460-A1 SELECTIVE ACYLATION METHOD NOVO NORDISK A/S (DK) 1998-01-22 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 (3 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-20060199763-A1 Derivatives of GLP-1 analogs GLP1R, GIPR, IAPP ASAH1 1850/4885KMT2A 4314/4885HPGD 3166/4885
US-20090176700-A1 Derivatives Of GLP-1 Analogs GLP1R, GIPR, IAPP ASAH1 1850/4885KMT2A 4314/4885HPGD 3166/4885
US-20010011071-A1 DERIVATIVES OF GLP-1 ANALOGS GLP1R, GIPR, IAPP ASAH1 1850/4885KMT2A 4314/4885HPGD 3166/4885

“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.