SCHEMBL5069935

SCHEMBL5069935

C[SnH]C

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
SCHEMBL912754 0.58
Ethane SCHEMBL23044683 0.58
SCHEMBL29383995 0.50
SCHEMBL5383540 0.50
Ammonia Solution, Strong SCHEMBL29150614 0.50
Ethane SCHEMBL25340782 0.50
Iodomethane SCHEMBL2432501 0.50
SCHEMBL172102 0.50
Fluoride SCHEMBL4661412 0.50
SCHEMBL11550412 0.50

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7378034-B2 Acidity and dissociation; stability, for doping polymers, as electrolytes in batteries UNIVERSITE DE MONTREAL (CA) 2008-05-27 US disclosed
US-20070205388-A1 Acidity and dissociation; stability, for doping polymers, as electrolytes in batteries UNIVERSITE DE MONTREAL 2007-09-06 US disclosed
US-7223824-B2 Multinuclear transition metal compound and catalyst system including the same DAELIM INDUSTRIAL CO., LTD. (KR) 2007-05-29 US disclosed
US-20060004155-A1 Multinuclear transition metal compound and catalyst system including the same DAELIM INDUSTRIAL CO., LTD. 2006-01-05 US disclosed
US-20050158631-A1 Acidity and dissociation; stability, for doping polymers, as electrolytes in batteries ACEP INC. 2005-07-21 US disclosed
US-6841638-B2 Acidity and dissociation; stability, for doping polymers, as electrolytes in batteries ACEP INC. (CA) 2005-01-11 US disclosed
US-20040162362-A9 Acidity and dissociation; stability, for doping polymers, as electrolytes in batteries ARMAND MICHEL (CA) 2004-08-19 US disclosed
US-20030195269-A1 Acidity and dissociation; stability, for doping polymers, as electrolytes in batteries ARMAND MICHEL (CA) 2003-10-16 US disclosed
US-6548567-B2 Metal cation or onium salts of sulfonimide derivatives or the corresponding phosphorus derivatives; use in producing ion conducting materials or electrolytes, as catalysts and for doping polymers ARMAND MICHEL (CA) 2003-04-15 US disclosed
US-20020013381-A1 Metal cation or onium salts of sulfonimide derivatives or the corresponding phosphorus derivatives; use in producing ion conducting materials or electrolytes, as catalysts and for doping polymers ARMAND MICHEL (CA) 2002-01-31 US disclosed
US-6340716-B1 ELECTRODES, CONDUCTORS, CAPACITORS AND BATTERIES ACEP INC. (CA) 2002-01-22 US disclosed
US-5880302-A Organometallic compound TARGOR GMBH (DE) 1999-03-09 US disclosed
EP-0742225-A1 Organometallic compound HOECHST AKTIENGESELLSCHAFT (DE) 1996-11-13 EP disclosed