SCHEMBL8458982

SCHEMBL8458982

NCC(N)CCc1ccccn1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HRH1 P35367 2/20 0.60
GRIN2D O15399 1/20 0.47
GRIN3B O60391 1/20 0.47
GRIN1 Q05586 1/20 0.47
GRIN2A Q12879 1/20 0.47
GRIN2B Q13224 1/20 0.47
GRIN2C Q14957 1/20 0.47
GRIN3A Q8TCU5 1/20 0.47
HRH3 Q9Y5N1 2/20 0.46
ALDH1A1 P00352 2/20 0.44
LMNA P02545 1/20 0.44
TAAR1 Q96RJ0 1/20 0.44
ALOX15 P16050 1/20 0.44
CYP1A2 P05177 4/20 0.44
CYP2C19 P33261 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.42
CA12 O43570 1/20 0.42
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
CA9 Q16790 1/20 0.42

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
SCHEMBL8718335 0.87 HRH1 (0.63) HRH1GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL21510401 0.84 HRH1 (0.53) HRH1GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL8718337 0.83 HRH1 (0.62) HRH1GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL230643 0.81 GRIN2D (0.59) HRH1GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL22268527 0.80 HRH1 (0.58) HRH1GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL10771160 0.79 HRH1 (0.57) HRH1GRIN2DGRIN3BGRIN1GRIN2A
Hydrochloric Acid SCHEMBL15671474 0.79 GRIN2D (0.58) HRH1GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL6938906 0.79 HRH1 (0.57) HRH1GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL6532234 0.78 SMN1; SMN2 (0.51) HRH1GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL7971241 0.77 GRIN2D (0.47) HRH1GRIN2DGRIN3BGRIN1GRIN2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-1999039575-A2 SYNERGISTIC BIOCIDAL ACTIVITY OF TERNARY COMPLEXES OF NEGATIVELY -CHARGED BIOCIDES (COMPONENT A), TRANSITION METAL IONS (COMPONENT B), AND NEUTRAL CHELATORS (COMPONENT C) YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM (IL) 1999-08-12 WO claimed