SCHEMBL6585962

SCHEMBL6585962

CN1CC[C@@H]1COc1cncc(-c2ccsc2)c1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRNB2 P17787 18/20 0.61
CHRNB1 P11230 16/20 0.61
CHRNB4 P30926 16/20 0.61
CHRNA3 P32297 16/20 0.61
CHRNB3 Q05901 16/20 0.61
CHRNA4 P43681 2/20 0.57
DAPK3 O43293 1/20 0.56
ROCK2 O75116 1/20 0.56
PRKCG P05129 1/20 0.56
PIM1 P11309 1/20 0.56
RPS6KB1 P23443 1/20 0.56
AKT1 P31749 1/20 0.56
LIMK1 P53667 1/20 0.56
CDK5 Q00535 1/20 0.56
PRKCD Q05655 1/20 0.56
PAK1 Q13153 1/20 0.56
STK3 Q13188 1/20 0.56
ROCK1 Q13464 1/20 0.56
DYRK1A Q13627 1/20 0.56
CDC42BPA Q5VT25 1/20 0.56

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 SCHEMBL6589389 0.99 CHRNB2 (0.60) CHRNB2CHRNB1CHRNB4CHRNA3CHRNB3
SCHEMBL6583152 0.83 CHRNB2 (0.86) CHRNB2CHRNB1CHRNB4CHRNA3CHRNB3
Hydrochloric Acid SCHEMBL6584062 0.82 CHRNB2 (0.84) CHRNB2CHRNB1CHRNB4CHRNA3CHRNB3
SCHEMBL6589644 0.80 CHRNB2 (0.42) CHRNB2CHRNB1CHRNB4CHRNA3CHRNB3
SCHEMBL21535280 0.77 CYP11B1 (0.66) CHRNB2CHRNB1CHRNB4CHRNA3CHRNB3
SCHEMBL6585020 0.76 CHRNB1 (1.00) CHRNB2CHRNB1CHRNB4CHRNA3CHRNB3
SCHEMBL14311702 0.76 CHRNB1 (1.00) CHRNB2CHRNB1CHRNB4CHRNA3CHRNB3
SCHEMBL6583732 0.76 CHRNB1 (1.00) CHRNB2CHRNB1CHRNB4CHRNA3CHRNB3
SCHEMBL7408002 0.76 CHRNB2 (0.64) CHRNB2CHRNB1CHRNB4CHRNA3CHRNB3
SCHEMBL13308144 0.76 CHRNB2 (0.84) CHRNB2CHRNB1CHRNB4CHRNA3CHRNB3

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 10 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 claimed
US-6127386-A STIMULANTS, NEUROTRANSMITTERS, CHOLINERGIC AGENTS ABBOTT LABORATORIES (US) 2000-10-03 US claimed
EP-0934308-A1 3-PYRIDYLOXYMETHYL HETEROCYCLIC ETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION Abbott Laboratories (US) 1999-08-11 EP claimed
WO-1997046554-A1 3-PYRIDYLOXYMETHYL HETEROCYCLIC ETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION ABBOTT LABORATORIES (US) 1997-12-11 WO claimed
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
EP-0934308-A1 3-PYRIDYLOXYMETHYL HETEROCYCLIC ETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION Abbott Laboratories (US) 1999-08-11 EP disclosed
WO-1997046554-A1 3-PYRIDYLOXYMETHYL HETEROCYCLIC ETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION ABBOTT LABORATORIES (US) 1997-12-11 WO disclosed
US-5629325-A TREATMENT OF NERVOUS SYSTEM DISORDERS; NEURONAL NICOTINIC CHOLINERGIC COMPOUNDS ABBOTT LABORATORIES (US) 1997-05-13 US disclosed