SCHEMBL12201431

SCHEMBL12201431

NCC1COCCc2nc3cnc4ccccc4c3n21

nearest known ligand 0.33

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 2/20 0.33
ALDH1A1 P00352 1/20 0.33
GLA P06280 1/20 0.33
GAA P10253 1/20 0.33
HPGD P15428 1/20 0.33
HSD17B10 Q99714 1/20 0.33
LRRK2 Q5S007 7/20 0.33
TLR7 Q9NYK1 7/20 0.33
JAK1 P23458 4/20 0.32
JAK2 O60674 2/20 0.32
TYK2 P29597 1/20 0.32
JAK3 P52333 1/20 0.32
TLR8 Q9NR97 1/20 0.32
GPR3 P46089 1/20 0.31

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
SCHEMBL12020770 1.00 KDM4E (0.33) KDM4EALDH1A1GLAGAAHPGD
SCHEMBL10237145 0.89 KDM4E (0.36) KDM4EALDH1A1GLAGAAHPGD
SCHEMBL12201376 0.87 TLR7 (0.35) KDM4EALDH1A1GLAGAAHPGD
SCHEMBL12020703 0.87 TLR7 (0.35) KDM4EALDH1A1GLAGAAHPGD
SCHEMBL10237144 0.82 TAAR1 (0.33) KDM4ELRRK2TLR7
SCHEMBL10237146 0.81 TLR7 (0.46) TLR7TLR8
SCHEMBL12201398 0.77 ACACB (0.41) JAK1JAK2TYK2JAK3
SCHEMBL12020838 0.77 ACACB (0.41) JAK1JAK2TYK2JAK3
SCHEMBL1774432 0.77 ABL1 (0.37) KDM4EALDH1A1GLAGAAHPGD
SCHEMBL10123167 0.72 KDM4E (0.43) KDM4EALDH1A1GLAGAAHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8034938-B2 Imidazo[4,5-c]quinolines, 6,7,8,9-tetrahydroimidazo[4,5-c]quinolines, imidazo[4,5-c]naphthyridines, and 6,7,8,9-tetrahydroimidazo[4,5-c]naphthyridines) with a CH( R1) group in the fused ring at 1-position of imidazo ring; modulate immune response, by induction of cytokine biosynthesis or other mechanism 3M INNOVATIVE PROPERTIES COMPANY (US) 2011-10-11 US disclosed
US-20080085895-A1 Substituted Chiral Fused [1,2]Imidazo[4,5-C] Ring Compounds 3M INNOVATIVE PROPERTIES COMPANY 2008-04-10 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-20080085895-A1 Substituted Chiral Fused [1,2]Imidazo[4,5-C] Ring Compounds IFNG, IL4, IFNAR1 KDM4E 649/4885ALDH1A1 1204/4885GLA 4130/4885

“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.