SCHEMBL12201398

SCHEMBL12201398

CC(C)(C)OC(=O)NCC1COCCc2nc3cnc4ccccc4c3n21

nearest known ligand 0.41

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
ACACB O00763 17/20 0.41
ACACA Q13085 14/20 0.41
CKS1B P61024 1/20 0.38
SKP1 P63208 1/20 0.38
SKP2 Q13309 1/20 0.38
JAK2 O60674 1/20 0.38
JAK1 P23458 1/20 0.38
TYK2 P29597 1/20 0.38
JAK3 P52333 1/20 0.38
CYP1A2 P05177 1/20 0.36
CYP3A4 P08684 1/20 0.36
CYP2C9 P11712 1/20 0.36
BCHE P06276 1/20 0.36

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
SCHEMBL12020838 1.00 ACACB (0.41) ACACBACACACKS1BSKP1SKP2
SCHEMBL12020795 0.85 TLR7 (0.44) ACACBACACA
SCHEMBL12020677 0.83 ACACB (0.37) ACACBACACABCHE
SCHEMBL9979366 0.81 CPB2 (0.40) ACACBACACAJAK2JAK1TYK2
SCHEMBL2513228 0.81 CPB2 (0.40) ACACBACACAJAK2JAK1TYK2
SCHEMBL10237145 0.79 KDM4E (0.36) JAK2JAK1TYK2JAK3
SCHEMBL12020703 0.77 TLR7 (0.35) JAK2JAK1TYK2JAK3
SCHEMBL12201376 0.77 TLR7 (0.35) JAK2JAK1TYK2JAK3
SCHEMBL12201431 0.77 KDM4E (0.33) JAK2JAK1TYK2JAK3
SCHEMBL12020770 0.77 KDM4E (0.33) JAK2JAK1TYK2JAK3

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 ACACB 3342/4885ACACA 2871/4885CKS1B 648/4885

“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.