SCHEMBL5350335

SCHEMBL5350335

CCCCCCC(=O)Nc1cnc2ccccc2c1NCCCCCSC

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EP300 Q09472 1/20 0.46
ALDH1A1 P00352 5/20 0.46
KDM4E B2RXH2 4/20 0.46
HPGD P15428 4/20 0.46
GAA P10253 3/20 0.46
HSD17B10 Q99714 3/20 0.45
TSHR P16473 2/20 0.45
GLA P06280 1/20 0.45
MAPK1 P28482 1/20 0.45
CETP P11597 1/20 0.45
LMNA P02545 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.42
S1PR2 O95136 1/20 0.42
NPSR1 Q6W5P4 1/20 0.42
SOAT1 P35610 2/20 0.42
SPHK2 Q9NRA0 1/20 0.41
SPHK1 Q9NYA1 1/20 0.41
HDAC3 O15379 1/20 0.40
HDAC1 Q13547 1/20 0.40
SLC2A1 P11166 1/20 0.40

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
SCHEMBL5349681 0.82 HRH3 (0.39) TOP2AMEN1PKMKMT2A
SCHEMBL5357183 0.78 ALDH1A1 (0.46) ALDH1A1HPGDLMNAHDAC3HDAC1
Hydrochloric Acid SCHEMBL1895255 0.78 ALDH1A1 (0.42) EP300ALDH1A1KDM4EHPGDGAA
SCHEMBL6500635 0.76 EP300 (0.57) EP300ALDH1A1KDM4EHPGDGAA
SCHEMBL24604572 0.75 ALDH1A1 (0.46) EP300ALDH1A1KDM4EHPGDGAA
SCHEMBL26981100 0.74 HPGD (0.47) EP300ALDH1A1KDM4EHPGDGAA
SCHEMBL4308968 0.74 MEN1 (0.45) ALDH1A1KDM4EHSD17B10TSHRMAPK1
SCHEMBL6411140 0.74 HRH3 (0.46) LMNASMN1; SMN2S1PR2NPSR1SLC2A1
SCHEMBL26981080 0.72 ALDH1A1 (0.48) EP300ALDH1A1KDM4EHPGDGAA
SCHEMBL26981132 0.72 EGFR (0.47) ALDH1A1KDM4EHPGDGAAHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
US-6949649-B2 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES CO. (US) 2005-09-27 US disclosed
US-20050209267-A1 Thioether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2005-09-22 US disclosed
US-20050209268-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-1541572-A1 Thioether substituted imidazoquinolines 3M Innovative Properties Company (US) 2005-06-15 EP disclosed
EP-1341791-B1 THIOETHER SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES CO (US) 2005-05-25 EP 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 (6 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 EP300 2093/4885ALDH1A1 2256/4885KDM4E 1675/4885
US-20050209268-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 EP300 2093/4885ALDH1A1 2256/4885KDM4E 1675/4885
US-20040097736-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 EP300 2093/4885ALDH1A1 2256/4885KDM4E 1675/4885
US-20020173655-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 EP300 2093/4885ALDH1A1 2256/4885KDM4E 1675/4885
US-20040102471-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 EP300 2093/4885ALDH1A1 2256/4885KDM4E 1675/4885
US-20030100764-A1 Thioether substituted imidazoquinolines IFNG, IRF3, IL2 EP300 2093/4885ALDH1A1 2256/4885KDM4E 1675/4885

“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.