SCHEMBL1490764

SCHEMBL1490764

CSCCCCCc1nc2ccccc2c(N)c1N

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 5/20 0.43
KDM4E B2RXH2 5/20 0.43
ALDH1A1 P00352 5/20 0.43
HPGD P15428 4/20 0.43
HSD17B10 Q99714 4/20 0.43
GLA P06280 3/20 0.43
CASP1 P29466 3/20 0.43
CASP7 P55210 3/20 0.43
ACHE P22303 2/20 0.43
CHRM2 P08172 1/20 0.43
ADRA2A P08913 1/20 0.43
ADORA3 P0DMS8 1/20 0.43
CHRM1 P11229 1/20 0.43
NQO2 P16083 1/20 0.43
MAOA P21397 1/20 0.43
DRD1 P21728 1/20 0.43
SLC6A2 P23975 1/20 0.43
ADRA1A P35348 1/20 0.43
OPRM1 P35372 1/20 0.43
KCNH2 Q12809 1/20 0.43

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
SCHEMBL5355323 0.88 ALDH1A1 (0.48) SMN1; SMN2KDM4EALDH1A1HPGDHSD17B10
SCHEMBL5355650 0.84 ALDH1A1 (0.42) SMN1; SMN2KDM4EALDH1A1HPGDHSD17B10
SCHEMBL15923395 0.84 KDM4E (0.55) SMN1; SMN2KDM4EALDH1A1HPGDHSD17B10
SCHEMBL5350898 0.81 ACHE (0.47) SMN1; SMN2KDM4EALDH1A1HPGDHSD17B10
SCHEMBL5358672 0.81 ACHE (0.47) SMN1; SMN2KDM4EALDH1A1HPGDHSD17B10
SCHEMBL3861838 0.80 DHFR (0.45)
SCHEMBL4320768 0.79 ACHE (0.48) SMN1; SMN2KDM4EALDH1A1HPGDHSD17B10
SCHEMBL5356465 0.77 ACHE (0.50) SMN1; SMN2KDM4EALDH1A1HPGDHSD17B10
SCHEMBL29099837 0.77 KMT2A (0.51) SMN1; SMN2KDM4EALDH1A1HPGDHSD17B10
SCHEMBL5455544 0.77 ALDH1A1 (0.46) SMN1; SMN2KDM4EALDH1A1HPGDHSD17B10

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 23 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7897767-B2 Oxime substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY (US) 2011-03-01 US disclosed
US-20090042925-A1 OXIME SUBSTITUTED IMIDAZOQUINOLINES COLEY PHARMACEUTICAL GROUP, INC. 2009-02-12 US disclosed
EP-1685129-A4 OXIME SUBSTITUTED IMIDAZO RING COMPOUNDS 3M INNOVATIVE PROPERTIES CO (US) 2008-10-22 EP disclosed
US-7288550-B2 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY (US) 2007-10-30 US disclosed
US-7276515-B2 Thioether substituted imidazoquinolines COLEY PHARMACEUTICAL GROUP, INC. (US) 2007-10-02 US disclosed
EP-1685129-A2 OXIME SUBSTITUTED IMIDAZO RING COMPOUNDS 3M Innovative Properties Company (US) 2006-08-02 EP disclosed
US-6949649-B2 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES CO. (US) 2005-09-27 US disclosed
US-20050209268-A1 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2005-09-22 US disclosed
US-20050209267-A1 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2005-09-22 US disclosed
US-6921826-B2 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES CO. (US) 2005-07-26 US disclosed
EP-1451191-A1 THIOETHER SUBSTITUTED IMIDAZOQUINOLINES 3M Innovative Properties Company (US) 2004-09-01 EP disclosed
US-20040102471-A1 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2004-05-27 US disclosed
US-20040097736-A1 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2004-05-20 US disclosed
US-6667312-B2 Useful as immune response modifiers 3M INNOVATIVE PROPERTIES COMPANY 2003-12-23 US disclosed
US-6664264-B2 Thioether substituted imidazoquinoline or tetrahydroimdazoquinoline compounds induce the biosynthesis of cytokines such as interferon and useful for treating viral disease in an animal 3M INNOVATIVE PROPERTIES COMPANY 2003-12-16 US disclosed
EP-1341791-A2 THIOETHER SUBSTITUTED IMIDAZOQUINOLINES 3M Innovative Properties Company (US) 2003-09-10 EP disclosed
WO-2003050121-A1 THIOETHER SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES COMPANY (US) 2003-06-19 WO disclosed
US-20030100764-A1 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2003-05-29 US disclosed
US-20020173655-A1 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2002-11-21 US disclosed
WO-2002046192-A2 THIOETHER SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES COMPANY (US) 2002-06-13 WO 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 (7 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-20050209267-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 SMN1; SMN2 3375/4885KDM4E 1675/4885ALDH1A1 2256/4885
US-20090042925-A1 OXIME SUBSTITUTED IMIDAZOQUINOLINES IFNG, IL2, IRF3 SMN1; SMN2 2541/4885KDM4E 1032/4885ALDH1A1 1493/4885
US-20050209268-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 SMN1; SMN2 3375/4885KDM4E 1675/4885ALDH1A1 2256/4885
US-20040097736-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 SMN1; SMN2 3375/4885KDM4E 1675/4885ALDH1A1 2256/4885
US-20020173655-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 SMN1; SMN2 3375/4885KDM4E 1675/4885ALDH1A1 2256/4885
US-20040102471-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 SMN1; SMN2 3375/4885KDM4E 1675/4885ALDH1A1 2256/4885
US-20030100764-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 SMN1; SMN2 3375/4885KDM4E 1675/4885ALDH1A1 2256/4885

“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.