SCHEMBL433508

SCHEMBL433508

[N].[N].[Ru]

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL62791 1.00
SCHEMBL379456 1.00
SCHEMBL6942614 1.00
SCHEMBL3797561 1.00
SCHEMBL6323473 0.82
SCHEMBL4459009 0.82
SCHEMBL1900488 0.82
SCHEMBL5886595 0.82
Phosphine SCHEMBL165123 0.82
Phosphine SCHEMBL5682224 0.82

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 27 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116789627-A Method for synthesizing chiral flavanol compound through dynamic kinetic resolution 中国科学院大连化学物理研究所 2023-09-22 CN claimed
EP-0829006-B1 PROCESS FOR PRODUCING A SENSITIVE SINGLE-LAYER SYSTEM FOR MEASURING THE CONCENTRATION OF ANALYTES AND A SYSTEM PRODUCED BY SAID PROCESS KIRSCHNER UWE (DE) 2003-08-20 EP claimed
CN-118005697-A Metal diamine complex with phosphorus chiral ligand framework, and preparation method and application thereof 绍兴赜军生物医药科技有限公司 2024-05-10 CN disclosed
CN-116789627-A Method for synthesizing chiral flavanol compound through dynamic kinetic resolution 中国科学院大连化学物理研究所 2023-09-22 CN disclosed
CN-116789627-A Method for synthesizing chiral flavanol compound through dynamic kinetic resolution 中国科学院大连化学物理研究所 2023-09-22 CN disclosed
EP-2595966-B1 SYNTHESIS OF CYCLOPENTAQUINAZOLINES BTG INT LTD (GB) 2020-10-28 EP disclosed
US-10385084-B2 Iron(II) catalysts containing tridentate PNP ligands, their synthesis, and use thereof THE GOVERNING COUNCIL OF THE UNIVERSITY OF TORONTO (CA) 2019-08-20 US disclosed
CN-106660029-A Iron (II) catalysts containing tridentate PNP ligands, their synthesis, and use thereof 多伦多大学管理委员会 2017-05-10 CN disclosed
EP-3092075-A1 IRON(II) CATALYSTS CONTAINING TRIDENTATE PNP LIGANDS, THEIR SYNTHESIS, AND USE THEREOF The Governing Council Of The University Of Toronto (CA) 2016-11-16 EP disclosed
US-20160326202-A1 IRON(II) CATALYSTS CONTAINING TRIDENTATE PNP LIGANDS, THEIR SYNTHESIS, AND USE THEREOF THE GOVERNING COUNCIL OF THE UNIVERSITY OF TORONTO (CA) 2016-11-10 US disclosed
US-20140288040-A1 SUBSTITUTED BENZYLAMINE COMPOUNDS, THEIR USE IN MEDICINE, AND IN PARTICULAR THE TREATMENT OF HEPATITIS C VIRUS (HCV) INFECTION ASTEX THERAPEUTICS LIMITED (GB) 2014-09-25 US disclosed
US-8039675-B2 Catalysts JOHNSON MATTHEY PLC (GB) 2011-10-18 US disclosed
US-20100197976-A1 CATALYSTS JOHNSON MATTHEY PLC (GB) 2010-08-05 US disclosed
EP-1849792-B1 Biphosphine ruthenium complexes with chiral diamine ligands as catalysts JOHNSON MATTHEY PLC (GB) 2008-12-10 EP disclosed
EP-1849792-A1 Biphosphine ruthenium complexes with chiral diamine ligands as catalysts Johnson Matthey PLC (GB) 2007-10-31 EP disclosed
EP-1651657-B1 BIPHOSPHINE RUTHENIUM COMPLEXES WITH CHIRAL DIAMINE LIGANDS AS CATALYSTS JOHNSON MATTHEY PLC (GB) 2007-08-22 EP disclosed
US-20070066850-A1 Catalysts JOHNSON MATTHEY PLC (GB) 2007-03-22 US disclosed
EP-1651657-A2 BIPHOSPHINE RUTHENIUM COMPLEXES WITH CHIRAL DIAMINE LIGANDS AS CATALYSTS Johnson Matthey PLC (GB) 2006-05-03 EP disclosed
WO-2005007662-A2 BIPHOSPHINE RUTHENIUM COMPLEXES WITH CHIRAL DIAMINE LIGANDE AS CATALYSTS JOHNSON MATTHEY PLC (GB) 2005-01-27 WO disclosed
JP-2000327646-A RUTHENIUM DIAMMONIUM SALT OF DIETHYLENETRIAMINEPENTAACETATIC ACID OR ITS HYDRATE, AND ITS PRODUCTION CHUBU KIRESUTO KK 2000-11-28 JP disclosed