SCHEMBL279742

SCHEMBL279742

CC(=O)CCCN1CCCCC1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.67
MAPK1 P28482 1/20 0.67
SMN1; SMN2 Q16637 1/20 0.67
PAOX Q6QHF9 2/20 0.60
ALDH1A1 P00352 3/20 0.54
MAPT P10636 3/20 0.54
POLB P06746 1/20 0.54
HRH3 Q9Y5N1 2/20 0.52
L3MBTL1 Q9Y468 1/20 0.52
ALOX15 P16050 1/20 0.47
FPR3 P25089 2/20 0.46
FPR2 P25090 2/20 0.46
LMNA P02545 1/20 0.44
HTR1A P08908 1/20 0.44
ADRA2A P08913 1/20 0.44
CYP2D6 P10635 1/20 0.44
ADRA2C P18825 1/20 0.44
OPRK1 P41145 1/20 0.44
KCNH2 Q12809 1/20 0.44
EBP Q15125 1/20 0.44

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
Hydrochloric Acid SCHEMBL11824629 0.98 CYP1A2 (0.64) CYP1A2MAPK1SMN1; SMN2PAOXALDH1A1
SCHEMBL805269 0.98 CYP1A2 (0.63) CYP1A2MAPK1SMN1; SMN2PAOXALDH1A1
Hydrochloric Acid SCHEMBL15169053 0.96 CYP1A2 (0.61) CYP1A2MAPK1SMN1; SMN2PAOXALDH1A1
SCHEMBL12522442 0.94 PAOX (0.69) CYP1A2MAPK1SMN1; SMN2PAOXALDH1A1
Hydrochloric Acid SCHEMBL5205856 0.91 PAOX (0.60) CYP1A2MAPK1SMN1; SMN2PAOXALDH1A1
Hydrochloric Acid SCHEMBL15168995 0.89 PAOX (0.69) CYP1A2MAPK1SMN1; SMN2PAOXALDH1A1
SCHEMBL1286683 0.86 ALDH1A1 (0.64) CYP1A2MAPK1SMN1; SMN2PAOXALDH1A1
SCHEMBL13993956 0.86 ALDH1A1 (0.64) CYP1A2MAPK1SMN1; SMN2PAOXALDH1A1
SCHEMBL23373543 0.86 PAOX (0.59) CYP1A2MAPK1SMN1; SMN2PAOXALDH1A1
Hydrochloric Acid SCHEMBL29360031 0.84 ALDH1A1 (0.61) CYP1A2MAPK1SMN1; SMN2PAOXALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230303514-A1 TLR7/8 ANTAGONISTS AND USES THEREOF MERCK PATENT GMBH (DE) 2023-09-28 US disclosed
US-20230303514-A1 TLR7/8 ANTAGONISTS AND USES THEREOF MERCK PATENT GMBH (DE) 2023-09-28 US disclosed
WO-2020251971-A1 SMARCA DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. (US) 2020-12-17 WO disclosed
US-10844459-B2 Process for extracting and recovering tantalum present in an acid aqueous phase by means of an ionic liquid, and use of such an ionic liquid for extracting the tantalum from an acid aqueous phase CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2020-11-24 US disclosed
US-10844459-B2 Process for extracting and recovering tantalum present in an acid aqueous phase by means of an ionic liquid, and use of such an ionic liquid for extracting the tantalum from an acid aqueous phase CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2020-11-24 US disclosed
EP-3334846-B1 PROCESSES FOR EXTRACTING AND RECOVERING TANTALUM PRESENT IN AN ACID AQUEOUS PHASE BY MEANS OF AN IONIC LIQUID, AND USE OF SUCH AN IONIC LIQUID FOR EXTRACTING THE TANTALUM FROM AN ACID AQUEOUS PHASE CENTRE NAT RECH SCIENT (FR) 2020-10-14 EP disclosed
EP-3334846-B1 PROCESSES FOR EXTRACTING AND RECOVERING TANTALUM PRESENT IN AN ACID AQUEOUS PHASE BY MEANS OF AN IONIC LIQUID, AND USE OF SUCH AN IONIC LIQUID FOR EXTRACTING THE TANTALUM FROM AN ACID AQUEOUS PHASE CENTRE NAT RECH SCIENT (FR) 2020-10-14 EP disclosed
US-20180221279-A1 MODIFIED DRUGS FOR USE IN LIPOSOMAL NANOPARTICLES UNIV BRITISH COLUMBIA (CA) 2018-08-09 US disclosed
EP-3334846-A1 PROCESSES FOR EXTRACTING AND RECOVERING TANTALUM PRESENT IN AN ACID AQUEOUS PHASE BY MEANS OF AN IONIC LIQUID, AND USE OF SUCH AN IONIC LIQUID FOR EXTRACTING THE TANTALUM FROM AN ACID AQUEOUS PHASE Centre National De La Recherche Scientifique (FR) 2018-06-20 EP disclosed
US-9968554-B2 Modified drugs for use in liposomal nanoparticles THE UNIVERSITY OF BRITISH COLUMBIA (CA) 2018-05-15 US disclosed
US-7795267-B2 Bicyclic piperazine compound having TGR23 antagonistic activity TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2010-09-14 US disclosed
US-7795267-B2 Bicyclic piperazine compound having TGR23 antagonistic activity TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2010-09-14 US disclosed
US-7569588-B2 Biphenyl compounds useful as muscarinic receptor antagonists THERAVANCE, INC. (US) 2009-08-04 US disclosed
US-7569588-B2 Biphenyl compounds useful as muscarinic receptor antagonists THERAVANCE, INC. (US) 2009-08-04 US disclosed
US-20090176767-A1 BIPHENYL COMPOUNDS USEFUL AS MUSCARINIC RECEPTOR ANTAGONISTS THERAVANCE BIOPHARMA R&D IP, LLC 2009-07-09 US disclosed
US-20090176767-A1 BIPHENYL COMPOUNDS USEFUL AS MUSCARINIC RECEPTOR ANTAGONISTS THERAVANCE BIOPHARMA R&D IP, LLC 2009-07-09 US disclosed
US-20080312224-A1 Oxaphenanthrene Derivatives MERCK PATENT GMBH (DE) 2008-12-18 US disclosed
US-7288552-B2 Piperidine derivatives, process for preparation thereof, and pharmaceutical composition for alzheimer's disease containing the same STC NARA CO., LTD. (KR) 2007-10-30 US disclosed
US-20070072865-A1 Bicyclic piperazine compound and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2007-03-29 US disclosed
US-20070072865-A1 Bicyclic piperazine compound and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2007-03-29 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 (5 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-20230303514-A1 TLR7/8 ANTAGONISTS AND USES THEREOF TLR7, TLR8, TLR9 CYP1A2 2103/4885MAPK1 549/4885SMN1; SMN2 1984/4885
US-20080312224-A1 Oxaphenanthrene Derivatives CYP3A43, CYP1A1, CYP1A2 CYP1A2 3/4885MAPK1 3176/4885SMN1; SMN2 4610/4885
US-20090176767-A1 BIPHENYL COMPOUNDS USEFUL AS MUSCARINIC RECEPTOR ANTAGONISTS CHRM2, CHRM1, CHRM3 CYP1A2 333/4885MAPK1 3316/4885SMN1; SMN2 4181/4885
US-20180221279-A1 MODIFIED DRUGS FOR USE IN LIPOSOMAL NANOPARTICLES ABCB11, SLC47A1, ABCB1 CYP1A2 4232/4885MAPK1 2101/4885SMN1; SMN2 985/4885
US-20070072865-A1 Bicyclic piperazine compound and use thereof GPR3, FFAR3, LPAR3 CYP1A2 783/4885MAPK1 3526/4885SMN1; SMN2 4533/4885

“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.