SCHEMBL12201463

SCHEMBL12201463

Cc1nc(N(Cc2ccccc2)Cc2ccccc2)c([N+](=O)[O-])c(N[C@@H](CNC(=O)OC(C)(C)C)COP)c1C

nearest known ligand 0.38

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
SYK P43405 1/20 0.38
AKT1 P31749 3/20 0.33
BRD4 O60885 1/20 0.33
APP P05067 2/20 0.33
ATM Q13315 1/20 0.33
LMNA P02545 2/20 0.32
SMN1; SMN2 Q16637 2/20 0.32
CTSL P07711 2/20 0.31
CTSB P07858 2/20 0.31
CTSS P25774 2/20 0.31
MMP1 P03956 1/20 0.31
MMP2 P08253 1/20 0.31
MMP9 P14780 1/20 0.31
MMP8 P22894 1/20 0.31
MMP13 P45452 1/20 0.31
MAPT P10636 1/20 0.31
MAPK1 P28482 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
L3MBTL1 Q9Y468 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
SCHEMBL12201460 0.81 POLB (0.36) SYKBRD4
SCHEMBL4301033 0.81 KMT2A (0.45) AKT1LMNASMN1; SMN2CTSLCTSB
SCHEMBL14208874 0.81 POLB (0.36) SYKBRD4
SCHEMBL6096675 0.80 BRD4 (0.41) BRD4MAPT
SCHEMBL5793540 0.73 KMT2A (0.40) LMNASMN1; SMN2MAPTMAPK1TDP1
SCHEMBL5793537 0.73 KMT2A (0.40) LMNASMN1; SMN2MAPTMAPK1TDP1
SCHEMBL6094679 0.73 BRD4 (0.40) BRD4MAPT
SCHEMBL4307213 0.72 GAA (0.43) AKT1LMNASMN1; SMN2CTSLCTSB
SCHEMBL14208872 0.72 BRD4 (0.33) SYKBRD4
SCHEMBL5818571 0.71 LMNA (0.36) AKT1LMNASMN1; SMN2MAPTMAPK1

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 SYK 2360/4885AKT1 2688/4885BRD4 375/4885

“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.