SCHEMBL9326191

SCHEMBL9326191

CNC(=O)Oc1ccc(OC)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 4/20 0.59
GAA P10253 2/20 0.59
ALDH1A1 P00352 2/20 0.59
HTT P42858 1/20 0.59
PLK1 P53350 1/20 0.59
CA1 P00915 6/20 0.52
CA2 P00918 6/20 0.52
NPC1 O15118 3/20 0.51
RAB9A P51151 3/20 0.51
TAAR1 Q96RJ0 1/20 0.51
CES2 O00748 1/20 0.50
CES1 P23141 1/20 0.50
CA12 O43570 1/20 0.48
CA7 P43166 1/20 0.48
CA9 Q16790 1/20 0.48
CA14 Q9ULX7 1/20 0.48
CYP1A2 P05177 2/20 0.47
CYP2C9 P11712 2/20 0.47
CYP2C19 P33261 2/20 0.47
LMNA P02545 1/20 0.47

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
SCHEMBL12893245 0.91 ALDH1A1 (0.51) SMN1; SMN2GAAALDH1A1HTTPLK1
SCHEMBL12793824 0.88 PKM (0.63) SMN1; SMN2GAAALDH1A1HTTPLK1
SCHEMBL28097321 0.83 ALDH1A1 (0.48) SMN1; SMN2GAAALDH1A1HTTPLK1
SCHEMBL27513052 0.83 KDM4E (0.53) SMN1; SMN2GAAALDH1A1HTTCA1
SCHEMBL2182880 0.83 LMNA (0.59) SMN1; SMN2GAAALDH1A1NPC1RAB9A
SCHEMBL6924040 0.81 ALDH1A1 (0.51) SMN1; SMN2GAAALDH1A1NPC1RAB9A
SCHEMBL2540440 0.81 ALDH1A1 (0.45) SMN1; SMN2GAAALDH1A1HTTNPC1
SCHEMBL20820013 0.81 MGLL (0.54) SMN1; SMN2GAAALDH1A1NPC1RAB9A
SCHEMBL11599136 0.81 ALDH1A1 (0.45) SMN1; SMN2GAAALDH1A1HTTNPC1
SCHEMBL188010 0.81 ALDH1A1 (0.55) SMN1; SMN2ALDH1A1NPC1RAB9ATAAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114853681-A Preparation method of pyrimidine heterocyclic guanyl formate compound 南京工业大学 2022-08-05 CN disclosed
US-9446139-B2 Polymer-based compositions and conjugates of HIV entry inhibitors NEKTAR THERAPEUTICS (US) 2016-09-20 US disclosed
US-8580919-B2 Polymer conjugates of GLP-1 NEKTAR THERAPEUTICS (US) 2013-11-12 US disclosed
US-8569267-B2 Tetracyclic tetrahydrofuran derivatives containing cyclic amine side chain JANSSEN PHARMACEUTICA, NV (BE) 2013-10-29 US disclosed
US-20130096258-A1 POLYMER CONJUGATES OF GLP-1 NEKTAR THERAPEUTICS (US) 2013-04-18 US disclosed
US-7879953-B2 Biobeneficial polyamide/polyethylene glycol polymers for use with drug eluting stents ADVANCED CARDIOVASCULAR SYSTEMS, INC. (US) 2011-02-01 US disclosed
US-7879953-B2 Biobeneficial polyamide/polyethylene glycol polymers for use with drug eluting stents ADVANCED CARDIOVASCULAR SYSTEMS, INC. (US) 2011-02-01 US disclosed
US-20100297211-A1 BIOBENEFICIAL POLYAMIDE/POLYETHYLENE GLYCOL POLYMERS FOR USE WITH DRUG ELUTING STENTS PACETTI STEPHEN D 2010-11-25 US disclosed
US-20100297211-A1 BIOBENEFICIAL POLYAMIDE/POLYETHYLENE GLYCOL POLYMERS FOR USE WITH DRUG ELUTING STENTS PACETTI STEPHEN D 2010-11-25 US disclosed
US-7786249-B2 Biobeneficial polyamide/polyethylene glycol polymers for use with drug eluting stents ADVANCED CARDIOVASCULAR SYSTEMS, INC. (US) 2010-08-31 US disclosed
US-20090012606-A1 BIOBENEFICIAL POLYAMIDE/POLYETHYLENE GLYCOL POLYMERS FOR USE WITH DRUG ELUTING STENTS PACETTI STEPHEN D 2009-01-08 US disclosed
US-20090012606-A1 BIOBENEFICIAL POLYAMIDE/POLYETHYLENE GLYCOL POLYMERS FOR USE WITH DRUG ELUTING STENTS PACETTI STEPHEN D 2009-01-08 US disclosed
US-20090012243-A1 BIOBENEFICIAL POLYAMIDE/POLYETHYLENE GLYCOL POLYMERS FOR USE WITH DRUG ELUTING STENTS PACETTI STEPHEN D 2009-01-08 US disclosed
US-20090012243-A1 BIOBENEFICIAL POLYAMIDE/POLYETHYLENE GLYCOL POLYMERS FOR USE WITH DRUG ELUTING STENTS PACETTI STEPHEN D 2009-01-08 US disclosed
US-20080262076-A1 Novel Tetracyclic Tetrahydrofuran Derivatives Containing Cyclic Amine Side Chain JANSSEN PHARMACEUTICA, NV (BE) 2008-10-23 US disclosed
US-20080262076-A1 Novel Tetracyclic Tetrahydrofuran Derivatives Containing Cyclic Amine Side Chain JANSSEN PHARMACEUTICA, NV (BE) 2008-10-23 US disclosed
US-7435788-B2 Biobeneficial polyamide/polyethylene glycol polymers for use with drug eluting stents ADVANCED CARDIOVASCULAR SYSTEMS, INC. (US) 2008-10-14 US disclosed
US-7435788-B2 Biobeneficial polyamide/polyethylene glycol polymers for use with drug eluting stents ADVANCED CARDIOVASCULAR SYSTEMS, INC. (US) 2008-10-14 US disclosed
US-7365196-B2 Sulphonamido-substituted bridged bicycloalkyl derivatives MERCK SHARP & DOHME LTD. (GB) 2008-04-29 US disclosed
US-5365691-A Methods and agents for combating cockroaches BAYER AKTIENGESELLSCHAFT (DE) 1994-11-22 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 (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-20130096258-A1 POLYMER CONJUGATES OF GLP-1 GLP1R, GIPR, NGLY1 SMN1; SMN2 2005/4885GAA 1701/4885ALDH1A1 2730/4885
US-20080262076-A1 Novel Tetracyclic Tetrahydrofuran Derivatives Containing Cyclic Amine Side Chain HTR2C, HTR2A, HTR5A SMN1; SMN2 1902/4885GAA 2907/4885ALDH1A1 848/4885

“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.