SCHEMBL528024

SCHEMBL528024

O=C([O-])c1ccnc(-c2cc(C(=O)[O-])ccn2)c1.O=C([O-])c1ccnc(-c2cc(C(=O)[O-])ccn2)c1.[Ru+2].[Ru+2]

nearest known ligand 0.61

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
KDM5C P41229 12/20 0.61
KDM2A Q9Y2K7 8/20 0.61
KDM3A Q9Y4C1 8/20 0.61
KDM4A O75164 8/20 0.61
KDM4C Q9H3R0 7/20 0.61
KDM4E B2RXH2 7/20 0.61
KDM6B O15054 4/20 0.52
P4HA1 P13674 1/20 0.50
KDM4B O94953 5/20 0.47
KDM5B Q9UGL1 5/20 0.47
JMJD6 Q6NYC1 2/20 0.46
P4HTM Q9NXG6 1/20 0.44
CA2 P00918 1/20 0.43
CA4 P22748 1/20 0.43
KMO O15229 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
SCHEMBL4848322 1.00 KDM5C (0.61) KDM5CKDM2AKDM3AKDM4AKDM4C
SCHEMBL2187195 1.00 KDM5C (0.61) KDM5CKDM2AKDM3AKDM4AKDM4C
SCHEMBL28374030 0.98 KDM5C (0.63) KDM5CKDM2AKDM3AKDM4AKDM4C
SCHEMBL15401893 0.96 KDM5C (0.61) KDM5CKDM2AKDM3AKDM4AKDM4C
SCHEMBL25273098 0.96 KDM5C (0.61) KDM5CKDM2AKDM3AKDM4AKDM4C
Lithium Ion SCHEMBL25269674 0.96 KDM5C (0.61) KDM5CKDM2AKDM3AKDM4AKDM4C
SCHEMBL25222959 0.96 KDM5C (0.61) KDM5CKDM2AKDM3AKDM4AKDM4C
SCHEMBL25219643 0.96 KDM5C (0.61) KDM5CKDM2AKDM3AKDM4AKDM4C
Potassium Ion SCHEMBL25270943 0.96 KDM5C (0.66) KDM5CKDM2AKDM3AKDM4AKDM4C
SCHEMBL8154522 0.96 KDM5C (0.61) KDM5CKDM2AKDM3AKDM4AKDM4C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220205991-A1 Controlled Generation of Measurable Signals and Uses Thereof RETELA LEASING, LLC 2022-06-30 US disclosed
US-7132598-B2 solar cells; organic electrically conducting agent exhibits a melting temperature TM which is lower than the operation temperature of the photoelectric conversion device SONY DEUTSCHLAND GMBH (DE) 2006-11-07 US disclosed
US-20050028862-A1 Light to enery conversion efficiency; gel electrolyte SONY DEUTSCHLAND GMBH (DE) 2005-02-10 US disclosed
US-20040177879-A1 Hole transporting agents and photoelectric conversion device comprising the same SONY DEUTSCHLAND GMBH (DE) 2004-09-16 US disclosed
EP-1456861-A1 A POLYMER GEL HYBRID SOLAR CELL Sony International (Europe) GmbH (DE) 2004-09-15 EP disclosed
US-6700058-B2 NANOPARTICULATE SEMICONDUCTOR SENSITIZED WITH A DYE; ORGANIC ELECTROCONDUCTOR IS TRIS(METHOXYPHENYL ETHYLHEXYLOXYPHENYL AMINO)BENZENE COMPOUND WITH MELTING TEMPERATURE LOWER THAN 140 C AND GLASS TRANSITION TEMPERATURE LOWER THAN 60 DEGREES C. SONY INTERNATIONAL (EUROPE) GMBH (DE) 2004-03-02 US disclosed
WO-2003054894-A1 A POLYMER GEL HYBRID SOLAR CELL SONY INTERNATIONAL (EUROPE) GMBH (DE) 2003-07-03 WO disclosed
US-20020036298-A1 Hole transporting agents and photoelectric conversion device comprising the same SONY DEUTSCHLAND GMBH (DE) 2002-03-28 US disclosed
EP-1160888-A1 Hole transporting agents and photoelectric conversion device comprising the same Sony International (Europe) GmbH (DE) 2001-12-05 EP disclosed
US-5463057-A Bi-pyridyl-rumetal complexes ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE, (EPFL) (CH) 1995-10-31 US disclosed