SCHEMBL29290952

SCHEMBL29290952

CC1=CC=CN(c2ccccn2)C1C=O

nearest known ligand 0.41

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.41
PDCD1 Q15116 1/20 0.35
CD274 Q9NZQ7 1/20 0.35
KDM4E B2RXH2 3/20 0.35
SLC11A2 P49281 3/20 0.35
ALKBH2 Q6NS38 1/20 0.35
EGLN1 Q9GZT9 1/20 0.35
MAPT P10636 2/20 0.34
ALDH1A1 P00352 1/20 0.34
THRB P10828 1/20 0.34
TDP1 Q9NUW8 1/20 0.34
CYP1A2 P05177 1/20 0.33
POLB P06746 1/20 0.33
CCNA2 P20248 3/20 0.33
CDK2 P24941 3/20 0.33
CRBN Q96SW2 1/20 0.33
EP300 Q09472 1/20 0.33
KAT2B Q92831 1/20 0.33

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
SCHEMBL28209858 0.83 SMN1; SMN2 (0.34) SMN1; SMN2KDM4ESLC11A2ALKBH2EGLN1
SCHEMBL28099962 0.83 CRBN (0.35) SMN1; SMN2KDM4EALKBH2EGLN1MAPT
SCHEMBL29290943 0.81 KDM4E (0.36) SMN1; SMN2PDCD1CD274KDM4ESLC11A2
SCHEMBL29290948 0.80 SLC11A2 (0.34) SMN1; SMN2PDCD1CD274KDM4ESLC11A2
SCHEMBL29290944 0.78 KDM4E (0.34) SMN1; SMN2PDCD1CD274KDM4ESLC11A2
SCHEMBL27504274 0.72 POLB (0.37) SMN1; SMN2PDCD1CD274KDM4ESLC11A2
SCHEMBL28565280 0.71 SMN1; SMN2 (0.34) SMN1; SMN2KDM4EMAPTALDH1A1CYP1A2
SCHEMBL29290947 0.71 SMN1; SMN2 (0.41) SMN1; SMN2PDCD1CD274KDM4ESLC11A2
SCHEMBL29290942 0.69 SMN1; SMN2 (0.41) SMN1; SMN2PDCD1CD274KDM4ESLC11A2
SCHEMBL20688977 0.66 MAP4K4 (0.38) SMN1; SMN2KDM4EALKBH2EGLN1MAPT

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
CN-109678854-A A kind of method that manganese catalyzes and synthesizes pyrido [1,2-a] indoles -6 (1H) -one class compound 陕西师范大学 2019-04-26 CN disclosed