SCHEMBL17130576

SCHEMBL17130576

C=C1/C=C\C(c2ccc(-c3ccc(-c4cnc5c(ccc6cccnc65)c4)cc3)cc2)=N/Cc2ncccc2/C=C\1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CCR1 P32246 2/20 0.39
▸ CCR5 P51681 2/20 0.39
▸ CCR8 P51685 2/20 0.39
▸ KDM4E B2RXH2 8/20 0.36
▸ GMNN O75496 1/20 0.36
▸ LMNA P02545 1/20 0.36
▸ TP53 P04637 1/20 0.36
▸ HSP90AA1 P07900 1/20 0.36
▸ MMP2 P08253 1/20 0.36
▸ CYP3A4 P08684 1/20 0.36
▸ CYP2D6 P10635 1/20 0.36
▸ MAPT P10636 1/20 0.36
▸ MMP9 P14780 1/20 0.36
▸ ALOX15 P16050 1/20 0.36
▸ TSHR P16473 1/20 0.36
▸ NFKB1 P19838 1/20 0.36
▸ MMP8 P22894 1/20 0.36
▸ THPO P40225 1/20 0.36
▸ MTOR P42345 1/20 0.36
▸ HTT P42858 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
SCHEMBL17934081 0.80 CCR1 (0.33) CCR1CCR5CCR8KDM4EGMNN
SCHEMBL11910132 0.76 CCR1 (0.62) CCR1CCR5CCR8KDM4EGMNN
SCHEMBL18806859 0.76 CCR1 (0.62) CCR1CCR5CCR8KDM4EGMNN
SCHEMBL17125609 0.76 CCR1 (0.62) CCR1CCR5CCR8KDM4EGMNN
SCHEMBL17146603 0.76 KDM4E (0.36) KDM4ELMNAMAPTHTTSMN1; SMN2
SCHEMBL23954363 0.73 CCR1 (0.67) CCR1CCR5CCR8KDM4EGMNN
SCHEMBL6357933 0.70 KDM4E (0.60) CCR1CCR5CCR8KDM4EGMNN
SCHEMBL18695363 0.70 CCR1 (0.54) CCR1CCR5CCR8KDM4EGMNN
SCHEMBL13045272 0.69 CCR1 (0.61) CCR1CCR5CCR8KDM4EGMNN
SCHEMBL17125608 0.69 CCR1 (0.53) CCR1CCR5CCR8KDM4EGMNN

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20150275076-A1 Non-crystallizable Pi-conjugated Molecular Glass Mixtures, Charge Transporting Molecular Glass Mixtures, Luminescent Molecular Glass Mixtures, or Combinations Thereof for Organic Light Emitting Diodes and other Organic Electronics and Photonics Applications Molaire Consulting 2015-10-01 — — US disclosed
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