SCHEMBL60797

SCHEMBL60797

Nc1ccc(CN2CCOCC2)cc1

nearest known ligand 0.71

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
HRH3 Q9Y5N1 4/20 0.71
ALDH1A1 P00352 2/20 0.66
LMNA P02545 2/20 0.61
SMN1; SMN2 Q16637 2/20 0.61
NOS3 P29474 1/20 0.57
NOS1 P29475 1/20 0.57
NOS2 P35228 1/20 0.57
MAPT P10636 1/20 0.56
KCNJ1 P48048 1/20 0.56
NCF1 P14598 1/20 0.54
AOC3 Q16853 1/20 0.53
HIF1A Q16665 2/20 0.51
EPAS1 Q99814 2/20 0.51
HPGD P15428 1/20 0.51
JAK2 O60674 1/20 0.51
PLK4 O00444 1/20 0.51
CYP2A13 Q16696 1/20 0.50

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
SCHEMBL23114261 0.98 HRH3 (0.69) HRH3ALDH1A1LMNASMN1; SMN2NOS3
Hydrochloric Acid SCHEMBL4468475 0.98 HRH3 (0.69) HRH3ALDH1A1LMNASMN1; SMN2NOS3
SCHEMBL13266893 0.94 HRH3 (0.82) HRH3ALDH1A1LMNASMN1; SMN2NOS3
SCHEMBL18747989 0.93 ALDH1A1 (0.68) HRH3ALDH1A1LMNASMN1; SMN2NOS3
SCHEMBL1647718 0.91 HRH3 (0.61) HRH3ALDH1A1LMNASMN1; SMN2NOS3
SCHEMBL13244883 0.90 HRH3 (0.59) HRH3ALDH1A1LMNASMN1; SMN2NOS3
SCHEMBL15467001 0.89 HRH3 (0.87) HRH3ALDH1A1LMNASMN1; SMN2NOS3
SCHEMBL7229968 0.89 HRH3 (0.56) HRH3ALDH1A1LMNASMN1; SMN2NOS3
SCHEMBL10690328 0.85 LMNA (0.80) HRH3ALDH1A1LMNANCF1
SCHEMBL27630736 0.85 HRH3 (0.67) HRH3ALDH1A1LMNASMN1; SMN2NOS3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103958482-B As the aminopyridine derivative of LRRK2 conditioning agents 健泰科生物技术公司 2017-06-09 CN claimed
CN-103539781-B A kind of synthetic method of WNT signal pathway inhibitor SUZHOU SOUTHEAST PHARMACEUTICALS CO., LTD. (CN) 2015-09-30 CN claimed
CN-103539781-A Method for synthesizing WNT (Wingless Int.) signal path inhibitor SOUTHEAST PHARMACEUTICALS CO LTD 2014-01-29 CN claimed
US-7579356-B2 Thia-tetraazaacenaphthylene kinase inhibitors JANSSEN PHARMACEUTICA NV (BE) 2009-08-25 US claimed
WO-2009026345-A1 THIAZOLIDINONE COMPOUNDS, AND METHODS OF MAKING AND USING SAME TARGEGEN INC. (US) 2009-02-26 WO claimed
US-7427625-B2 Substituted thiatriazaacenaphthylene-6-carbonitrile kinase inhibitors JANSSEN PHARMACEUTICA, N.V. (BE) 2008-09-23 US claimed
US-20080108611-A1 SUBSTITUTED THIENOPYRIMIDINE KINASE INHIBITORS JANSSEN PHARMACEUTICA N.V. (BE) 2008-05-08 US claimed
US-20070265264-A1 5-(3-chloro-4-fluoro-phenyl)-4-oxo-4,5-dihydro-3H-1-thia-3,5,6,8-tetraaza-acenaphthylene-2-carboxylic acid (3,4-dimethoxy-phenyl)-amide JANSSEN PHARMACEUTICA, N.V. (BE) 2007-11-15 US claimed
US-20070225309-A1 SUBSTITUTED THIATRIAZAACENAPHTHYLENE-6-CARBONITRILE KINASE INHIBITORS JANSSEN PHARMACEUTICA, N.V. (BE) 2007-09-27 US claimed
WO-2007092879-A2 SUBSTITUTED THIATRIAZAACENAPHTHYLENE-6-CARBONITRILE KINASE INHIBITORS JANSSEN PHARMACEUTICA, N.V. (BE) 2007-08-16 WO claimed
WO-2007084815-A2 SUBSTITUTED THIENOPYRIMIDINE KINASE INHIBITORS JANSSEN PHARMACEUTICA, N.V. (BE) 2007-07-26 WO claimed
WO-2006118749-A1 THIA-TETRAAZAACENAPHTHYLENE KINASE INHIBITORS JANSSEN PHARMACEUTICA, N.V. (BE) 2006-11-09 WO claimed
CN-116406355-B P38 alpha mitogen-activated protein kinase inhibitors GEN1E生命科学公司 2026-05-15 CN disclosed
CN-117120422-B Substituted naphthyl P38 alpha mitogen-activated protein kinase inhibitors GEN1E生命科学公司 2026-05-12 CN disclosed
US-12528810-B2 Small molecule inhibitors of DYRK/CLK and uses thereof ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA (US) 2026-01-20 US disclosed
EP-4676926-A1 BICYCLIC HETEROARYL COMPOUNDS FOR USE AS GPR35 MODULATORS ThirtyFiveBio Limited (GB) 2026-01-14 EP disclosed
EP-0790239-A1 Novel 4-phenyl-2-(piperazinyl/perhydrodiazepinyl/aminoalkyl)carbonylmethyl)-1,4-dihydropyridine-3,5-dicarboxylic acid derivatives as bradykinin receptor antagonists PFIZER INC. (US) 1997-08-20 EP disclosed
WO-1997012870-A1 TETRAHYDROQUINOLINES AS NMDA ANTAGONISTS GLAXO WELLCOME S.P.A. (IT) 1997-04-10 WO disclosed
US-5556969-A Benzodiazepine derivatives MERCK SHARP & DOHME LTD. (GB) 1996-09-17 US disclosed
WO-1996002510-A1 NOVEL 1-[4(AMINO METHYL)PHENYL] SUBSTITUTED QUINOLONE CARBOXYLIC ACIDS BAYER AKTIENGESELLSCHAFT (DE) 1996-02-01 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 (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-12528810-B2 Small molecule inhibitors of DYRK/CLK and uses thereof CLK3, CLK2, CLK1 HRH3 488/4885ALDH1A1 3885/4885LMNA 3740/4885
US-20070225309-A1 SUBSTITUTED THIATRIAZAACENAPHTHYLENE-6-CARBONITRILE KINASE INHIBITORS MAP3K11, MAP3K6, MAP4K2 HRH3 2500/4885ALDH1A1 2543/4885LMNA 2852/4885
US-20070265264-A1 5-(3-chloro-4-fluoro-phenyl)-4-oxo-4,5-dihydro-3H-1-thia-3,5,6,8-tetraaza-acenaphthylene-2-carboxylic acid (3,4-dimethoxy-phenyl)-amide ADK, MAP3K9, MAP4K5 HRH3 1681/4885ALDH1A1 924/4885LMNA 3244/4885
US-20080108611-A1 SUBSTITUTED THIENOPYRIMIDINE KINASE INHIBITORS MAP4K2, MAP3K6, MAP3K2 HRH3 1921/4885ALDH1A1 1988/4885LMNA 4421/4885

“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.