SCHEMBL6906334

SCHEMBL6906334

CCc1ccc2c(c1)Cc1ccccc1C2

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.48
CYP2A6 P11509 1/20 0.48
NPC1 O15118 3/20 0.46
RAB9A P51151 3/20 0.46
KDM4E B2RXH2 1/20 0.46
ALDH1A1 P00352 2/20 0.44
TSHR P16473 2/20 0.44
ATM Q13315 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
MAPK1 P28482 2/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
LMNA P02545 1/20 0.42
MAPT P10636 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
TP53 P04637 2/20 0.42
DRD2 P14416 5/20 0.41
DRD1 P21728 4/20 0.41
DRD5 P21918 3/20 0.41
DRD3 P35462 3/20 0.41
SLC6A2 P23975 2/20 0.41

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
SCHEMBL29737067 1.00 CYP1A2 (0.48) CYP1A2CYP2A6NPC1RAB9AKDM4E
SCHEMBL5357579 0.86 ALDH1A1 (0.59) CYP1A2CYP2A6NPC1RAB9AKDM4E
SCHEMBL4894905 0.82 ALDH1A1 (0.46) CYP1A2CYP2A6NPC1RAB9AKDM4E
SCHEMBL20491470 0.82 NPC1 (0.52) CYP1A2CYP2A6NPC1RAB9AKDM4E
SCHEMBL14447667 0.80 ALDH1A1 (0.64) CYP1A2NPC1RAB9AKDM4EALDH1A1
SCHEMBL31277051 0.80 ALDH1A1 (0.64) CYP1A2NPC1RAB9AKDM4EALDH1A1
Ethylbenzene SCHEMBL11059217 0.79 TP53 (0.70) CYP1A2CYP2A6NPC1RAB9AKDM4E
SCHEMBL31414400 0.79 CYP1A2 (0.45) CYP1A2CYP2A6NPC1RAB9AKDM4E
SCHEMBL2310400 0.78 TSHR (0.42) NPC1RAB9AALDH1A1TSHRATM
SCHEMBL28170845 0.77 ALDH1A1 (0.42) CYP1A2CYP2A6NPC1RAB9AKDM4E

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
CN-110590528-B Method for quantitatively converting 9, 10-dihydroanthracene into anthraquinone through selective oxidation of molecular oxygen driven by visible light 湖南师范大学 2022-07-01 CN claimed
CN-110590528-A Method for quantitatively converting 9, 10-dihydroanthracene into anthraquinone through selective oxidation of molecular oxygen driven by visible light 湖南师范大学 2019-12-20 CN claimed
CN-110590528-B Method for quantitatively converting 9, 10-dihydroanthracene into anthraquinone through selective oxidation of molecular oxygen driven by visible light 湖南师范大学 2022-07-01 CN disclosed
CN-110590528-A Method for quantitatively converting 9, 10-dihydroanthracene into anthraquinone through selective oxidation of molecular oxygen driven by visible light 湖南师范大学 2019-12-20 CN disclosed
US-6815481-B2 FUSED DIBENZO THERMAL STABILIZERS SUCH AS ANTHRACENE, XANTHENE AND ANTHRONE SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-11-09 US disclosed
US-6596896-B2 Reacting aromatic monohydroxy compound with carbon monoxide and oxygen in presence of palladium, redox catalyst, heteropoly acid, and quaternary ammonium or phosphonium salt; carbonation, dehydration TEIJIN LIMITED (JP) 2003-07-22 US disclosed
US-20030032831-A1 Process for producing aromatic carbonate TEIJIN LIMITED (JP) 2003-02-13 US disclosed
EP-1266883-A1 PROCESS FOR PRODUCING AROMATIC CARBONATE TEIJIN LIMITED (JP) 2002-12-18 EP disclosed
US-20020032256-A1 Polybutadiene composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-03-14 US disclosed