SCHEMBL2512643

SCHEMBL2512643

CC(C)(C)OC(=O)NC(CO)CCCNC(=O)OCc1ccccc1

nearest known ligand 0.63

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.63
SYK P43405 1/20 0.59
KLK7 P49862 2/20 0.54
KLK5 Q9Y337 2/20 0.54
HTT P42858 1/20 0.52
ITGB3 P05106 1/20 0.49
ITGA2B P08514 1/20 0.49
FOLH1 Q04609 2/20 0.48
ATM Q13315 1/20 0.48
LMNA P02545 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
TGM2 P21980 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
CTSK P43235 1/20 0.47

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
SCHEMBL21789935 1.00 MAPT (0.63) MAPTSYKKLK7KLK5HTT
SCHEMBL21790401 1.00 MAPT (0.63) MAPTSYKKLK7KLK5HTT
SCHEMBL8838459 0.97 MAPT (0.67) MAPTSYKKLK7KLK5HTT
SCHEMBL29401232 0.97 MAPT (0.67) MAPTSYKKLK7KLK5HTT
SCHEMBL30915257 0.97 MAPT (0.67) MAPTSYKKLK7KLK5HTT
SCHEMBL23161521 0.96 SYK (0.65) MAPTSYKKLK7KLK5HTT
SCHEMBL2512642 0.96 SYK (0.65) MAPTSYKKLK7KLK5HTT
SCHEMBL19301063 0.96 SYK (0.65) MAPTSYKKLK7KLK5HTT
SCHEMBL6620798 0.93 SYK (0.61) MAPTSYKKLK7KLK5HTT
SCHEMBL6619895 0.93 SYK (0.61) MAPTSYKKLK7KLK5HTT

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-8350034-B2 Substituted chiral fused [1,2]imidazo[4,5-C] ring compounds 3M INNOVATIVE PROPERTIES COMPANY (US) 2013-01-08 US disclosed
EP-1831221-B1 SUBSTITUTED CHIRAL FUSED 1,2 IMIDAZO 4,5-C RING COMPOUNDS 3M INNOVATIVE PROPERTIES CO (US) 2012-08-08 EP disclosed
US-20110293654-A1 SUBSTITUTED CHIRAL FUSED [1,2]IMIDAZO[4,5-c] RING COMPOUNDS 3M INNOVATIVE PROPERTIES COMANY 2011-12-01 US disclosed
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
CN-1434795-A Acylated Pseudodipeptides with Functionalized Auxiliary Branches OM PHARMA (CH) 2003-08-06 CN 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 (2 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-20110293654-A1 SUBSTITUTED CHIRAL FUSED [1,2]IMIDAZO[4,5-c] RING COMPOUNDS IFNG, IL4, IFNAR1 MAPT 4435/4885SYK 2360/4885KLK7 4018/4885
US-20080085895-A1 Substituted Chiral Fused [1,2]Imidazo[4,5-C] Ring Compounds IFNG, IL4, IFNAR1 MAPT 4435/4885SYK 2360/4885KLK7 4018/4885

“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.