SCHEMBL6996659

SCHEMBL6996659

COc1ccccc1Nc1cccc(N(C)C)c1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.51
MAPT P10636 3/20 0.51
MAPK1 P28482 2/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
ACP1 P24666 2/20 0.50
KDM1A O60341 1/20 0.48
EGFR P00533 2/20 0.46
NPC1 O15118 1/20 0.46
GAA P10253 1/20 0.46
RAB9A P51151 1/20 0.46
JAK2 O60674 1/20 0.46
FLT3 P36888 1/20 0.46
ERBB2 P04626 1/20 0.46
MAPK10 P53779 2/20 0.44
MAPK8 P45983 1/20 0.44
MAPK14 Q16539 1/20 0.44
FYN P06241 1/20 0.43
TNNI3K Q59H18 1/20 0.43
KDM4E B2RXH2 2/20 0.42
DHFR P00374 1/20 0.42

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
SCHEMBL9427888 0.85 MAPT (0.62) ALDH1A1MAPTMAPK1L3MBTL1EGFR
SCHEMBL5080732 0.78 MAPT (0.68) ALDH1A1MAPTMAPK1L3MBTL1EGFR
SCHEMBL7003346 0.78 KDM1A (0.50) ALDH1A1MAPTMAPK1ACP1KDM1A
SCHEMBL29744518 0.77 MAPT (0.72) ALDH1A1MAPTMAPK1L3MBTL1NPC1
SCHEMBL2095055 0.77 MAPT (0.72) ALDH1A1MAPTMAPK1L3MBTL1NPC1
SCHEMBL3030672 0.77 KDM1A (0.59) ALDH1A1MAPTMAPK1ACP1KDM1A
SCHEMBL600664 0.76 EGFR (0.45) ALDH1A1ACP1KDM1AEGFRJAK2
Hydrochloric Acid SCHEMBL7128944 0.76 MAPT (0.70) ALDH1A1MAPTMAPK1L3MBTL1NPC1
SCHEMBL28557487 0.76 KDM1A (0.63) ALDH1A1MAPTMAPK1L3MBTL1ACP1
SCHEMBL5923796 0.75 MAPT (0.81) ALDH1A1MAPTMAPK1L3MBTL1EGFR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6635602-B1 Heat sensitive and pressure sensitive recording material; synthesised directly by the reaction of two derivatives of amino phenols, phthalic anhydrides, keto acids and/or diphenylamines with a phenol derivative CIBA SPECIALTY CHEMICALS CORPORATION 2003-10-21 US disclosed
US-6566302-B1 For use in heat sensitive and pressure sensitive recording materials CIBA SPECIALTY CHEMICALS CORPORATION 2003-05-20 US disclosed
EP-1107972-B1 PREPARATION PROCESS FOR MANUFACTURE AND PURIFICATION OF MIXTURES OF FLUORAN COMPOUNDS AND RECORDING MATERIAL COMPRISING SAID MIXTURES OF FLUORAN CIBA SC HOLDING AG (CH) 2003-01-02 EP disclosed
EP-1115579-B1 MONOPHASE SOLID SOLUTIONS COMPRISING A PLURALITY OF COLOUR FORMER COMPOUNDS AND PROCESS FOR THEIR PREPARATION CIBA SC HOLDING AG (CH) 2002-11-20 EP disclosed
EP-1115579-A1 MONOPHASE SOLID SOLUTIONS COMPRISING A PLURALITY OF COLOUR FORMER COMPOUNDS AND PROCESS FOR THEIR PREPARATION Ciba SC Holding AG (CH) 2001-07-18 EP disclosed
EP-1107972-A1 PREPARATION PROCESS FOR MANUFACTURE AND PURIFICATION OF MIXTURES OF FLUORAN COMPOUNDS AND RECORDING MATERIAL COMPRISING SAID MIXTURES OF FLUORAN Ciba SC Holding AG (CH) 2001-06-20 EP disclosed
WO-2000026037-A1 HEAT SENSITIVE RECORDING MATERIAL CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2000-05-11 WO disclosed
WO-2000012513-A1 NOVEL PREPARATION PROCESS FOR MANUFACTURE AND PURIFICATION OF MIXTURES OF FLUORAN COMPOUNDS AND RECORDING MATERIAL COMPRISING SAID MIXTURES OF FLUORAN COMPOUNDS CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2000-03-09 WO disclosed
WO-2000012318-A1 MONOPHASE SOLID SOLUTIONS COMPRISING A PLURALITY OF COLOUR FORMER COMPOUNDS AND PROCESS FOR THEIR PREPARATION CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2000-03-09 WO disclosed