SCHEMBL4152265

SCHEMBL4152265

CN(C)c1ccc(-c2nc3c(C(=O)Nc4cccnc4)ccnc3[nH]2)cc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GSK3B P49841 4/20 0.56
AURKA O14965 1/20 0.47
BRAF P15056 1/20 0.46
EGLN1 Q9GZT9 1/20 0.45
NAMPT P43490 3/20 0.45
ALDH1A1 P00352 2/20 0.45
HTT P42858 1/20 0.45
CSF1R P07333 1/20 0.45
PARP1 P09874 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
KDM4E B2RXH2 2/20 0.43
MEN1 O00255 1/20 0.43
HPGD P15428 1/20 0.43
KMT2A Q03164 1/20 0.43
TSHR P16473 2/20 0.43
NPC1 O15118 2/20 0.42
RAB9A P51151 2/20 0.42
CYP11B2 P19099 1/20 0.42
LMNA P02545 1/20 0.42
GAA P10253 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
SCHEMBL4169328 0.89 GSK3B (0.55) GSK3BEGLN1NAMPTALDH1A1HTT
SCHEMBL4156450 0.86 GSK3B (0.74) GSK3BEGLN1ALDH1A1HTTL3MBTL1
SCHEMBL8237753 0.83 GSK3B (0.61) GSK3BAURKAPARP1MAPT
SCHEMBL4169308 0.82 GSK3B (0.52) GSK3BEGLN1NAMPTALDH1A1HTT
SCHEMBL4160814 0.81 LRRK2 (0.53) GSK3BAURKATSHRNPC1RAB9A
SCHEMBL4152109 0.81 GSK3B (0.53) GSK3BAURKAEGLN1ALDH1A1HTT
SCHEMBL4150197 0.80 GSK3B (0.75) GSK3BEGLN1NAMPTALDH1A1HTT
SCHEMBL4152912 0.80 TP53 (0.53) GSK3BPARP1KMT2ANPC1RAB9A
SCHEMBL4162865 0.79 GSK3B (0.56) GSK3BEGLN1NAMPTALDH1A1HTT
SCHEMBL4152155 0.79 GSK3B (0.48) GSK3BEGLN1ALDH1A1MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090170847-A1 Imidazopyridine Derivatives Inhibiting Protein Kinase Activity, Method for the Preparation Thereof and Pharmaceutical Composition Containing Same YUYU PHARMA, INC. (KR) 2009-07-02 US claimed
EP-1984370-A1 IMIDAZOPYRIDINE DERIVATIVES INHIBITING PROTEIN KINASE ACTIVITY, METHOD FOR THE PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITION CONTAINING SAME Crystalgenomics, Inc. (KR) 2008-10-29 EP claimed
WO-2007083978-A1 IMIDAZOPYRIDINE DERIVATIVES INHIBITING PROTEIN KINASE ACTIVITY, METHOD FOR THE PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITION CONTAINING SAME CRYSTALGENOMICS, INC. (KR) 2007-07-26 WO claimed
US-20090170847-A1 Imidazopyridine Derivatives Inhibiting Protein Kinase Activity, Method for the Preparation Thereof and Pharmaceutical Composition Containing Same YUYU PHARMA, INC. (KR) 2009-07-02 US disclosed
US-20090170847-A1 Imidazopyridine Derivatives Inhibiting Protein Kinase Activity, Method for the Preparation Thereof and Pharmaceutical Composition Containing Same YUYU PHARMA, INC. (KR) 2009-07-02 US disclosed
US-20090170847-A1 Imidazopyridine Derivatives Inhibiting Protein Kinase Activity, Method for the Preparation Thereof and Pharmaceutical Composition Containing Same YUYU PHARMA, INC. (KR) 2009-07-02 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20090170847-A1 Imidazopyridine Derivatives Inhibiting Protein Kinase Activity, Method for the Preparation Thereof and Pharmaceutical Composition Containing Same GSK3B, GSK3A, MAP3K3 GSK3B 1/4885AURKA 29/4885BRAF 335/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.