SCHEMBL6587463

SCHEMBL6587463

CC(C)(C)OC(=O)N1CC[C@H]1COc1cnc(Cl)c(C=Cc2ccncc2)c1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AKT1 P31749 2/20 0.48
CDC7 O00311 1/20 0.48
DAPK3 O43293 1/20 0.48
DYRK3 O43781 1/20 0.48
ROCK2 O75116 1/20 0.48
RPS6KA5 O75582 1/20 0.48
PRKD3 O94806 1/20 0.48
MAP4K4 O95819 1/20 0.48
PIM1 P11309 1/20 0.48
PHKG2 P15735 1/20 0.48
PRKACA P17612 1/20 0.48
RPS6KB1 P23443 1/20 0.48
MARK3 P27448 1/20 0.48
AKT2 P31751 1/20 0.48
PRKCI P41743 1/20 0.48
CSNK1A1 P48729 1/20 0.48
CSNK1D P48730 1/20 0.48
CLK2 P49760 1/20 0.48
GSK3A P49840 1/20 0.48
GSK3B P49841 1/20 0.48

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
SCHEMBL6581899 0.95 CHRNB1 (0.49) AKT1CDC7DAPK3DYRK3ROCK2
SCHEMBL6586068 0.95 CHRNB1 (0.49) AKT1CDC7DAPK3DYRK3ROCK2
SCHEMBL6581902 0.95 CHRNB1 (0.49) AKT1CDC7DAPK3DYRK3ROCK2
SCHEMBL6586070 0.95 CHRNB1 (0.49) AKT1CDC7DAPK3DYRK3ROCK2
SCHEMBL6585964 0.86 CHRNB2 (0.60) AKT1DAPK3DYRK3ROCK2RPS6KA5
SCHEMBL6588750 0.84 ALOX5AP (0.38) CHRNB4CHRNA3
SCHEMBL6583755 0.81 CHRNB2 (0.66) AKT1DYRK3ROCK2RPS6KA5PRKD3
SCHEMBL6583881 0.81 CHRNB2 (0.66) AKT1DYRK3ROCK2RPS6KA5PRKD3
SCHEMBL6583758 0.81 CHRNB2 (0.66) AKT1DYRK3ROCK2RPS6KA5PRKD3
SCHEMBL7470605 0.81 ALOX5AP (0.41) CHRNB2CHRNB4CHRNA3

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0934308-B1 3-PYRIDYLOXYMETHYL HETEROCYCLIC ETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION ABBOTT LAB (US) 2004-08-11 EP disclosed
US-6437138-B1 5-BROMO-6-CHLORO-3-(2-(S)-AZETIDINYL OR PYRROLIDINYL-METHOXY) PYRIDINE INTERMEDIATES FOR THE 5-SUBSTITUTED COMPOUNDS WHICH ARE POTENT LIGANDS AT NEURONAL NICOTINIC CHOLINERGIC CHANNEL RECEPTORS, NEUROTRANSMITTER CONTROLLING AGENTS ABBOTT LABORATORIES 2002-08-20 US disclosed
US-6127386-A STIMULANTS, NEUROTRANSMITTERS, CHOLINERGIC AGENTS ABBOTT LABORATORIES (US) 2000-10-03 US disclosed
US-5629325-A TREATMENT OF NERVOUS SYSTEM DISORDERS; NEURONAL NICOTINIC CHOLINERGIC COMPOUNDS ABBOTT LABORATORIES (US) 1997-05-13 US disclosed