SCHEMBL13628532

SCHEMBL13628532

CNOCCNc1ccccn1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2C19 P33261 1/20 0.56
CYP1A2 P05177 1/20 0.53
CXCR4 P61073 1/20 0.49
FABP1 P07148 1/20 0.47
FABP6 P51161 1/20 0.47
POLB P06746 1/20 0.43
NPC1 O15118 2/20 0.43
RAB9A P51151 2/20 0.43
GAA P10253 1/20 0.43
TP53 P04637 1/20 0.43
TSHR P16473 1/20 0.43
KDM4E B2RXH2 1/20 0.42
ALDH1A1 P00352 1/20 0.42
HPGD P15428 1/20 0.42
APP P05067 2/20 0.42
ITGB3 P05106 1/20 0.41
ITGB1 P05556 1/20 0.41
ITGAV P06756 1/20 0.41
ITGB5 P18084 1/20 0.41
ITGB6 P18564 1/20 0.41

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
SCHEMBL3647775 0.82 POLB (0.60) CYP2C19CYP1A2CXCR4FABP1FABP6
SCHEMBL29980727 0.82 POLB (0.60) CYP2C19CYP1A2CXCR4FABP1FABP6
SCHEMBL13628674 0.82 CYP2C19 (0.51) CYP2C19CYP1A2CXCR4FABP1FABP6
SCHEMBL3265804 0.79 CYP1A2 (0.70) CYP2C19CYP1A2CXCR4FABP1FABP6
SCHEMBL1344396 0.78 CYP2C19 (0.62) CYP2C19CYP1A2CXCR4FABP1FABP6
Hydrochloric Acid SCHEMBL8177967 0.77 CYP2C19 (0.61) CYP2C19CYP1A2CXCR4FABP1FABP6
SCHEMBL31015708 0.76 CYP2C19 (0.65) CYP2C19CYP1A2CXCR4FABP1FABP6
SCHEMBL20655751 0.76 CYP1A2 (0.61) CYP2C19CYP1A2CXCR4FABP1FABP6
SCHEMBL327850 0.76 CYP2C19 (0.65) CYP2C19CYP1A2CXCR4FABP1FABP6
SCHEMBL12954631 0.76 DRD2 (0.54) CYP2C19CYP1A2GAAKDM4EITGB3

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
US-7612197-B2 Reacting a nucleophil with OH group with an electrophil to form an adduct, reacting adduct with a reagent selected from oxidizing, sulfurizing or selenizing agents to produce hydroxy protected oligonucleotide, heating to deprotect hydroxy protecting group such as 2-(2-pyridyl)aminoethoxycarbonyl The United States of America as repesented by the Secretary of the Department of Health and Human Services (US) 2009-11-03 US disclosed