SCHEMBL55525

SCHEMBL55525

CC[Si](CC)(CC)[N][Si](CC)(CC)CC

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
SCHEMBL13380153 0.57
SCHEMBL8382158 0.57
SCHEMBL152107 0.53
SCHEMBL285825 0.53
SCHEMBL1525846 0.53
Ammonia Solution, Strong SCHEMBL14808976 0.50
SCHEMBL873438 0.50
SCHEMBL379483 0.50
SCHEMBL838621 0.50
SCHEMBL887922 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 157 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3135664-B1 ALKOXIDE COMPOUND, RAW MATERIAL FOR FORMING THIN FILM, METHOD FOR PRODUCING THIN FILM, AND ALCOHOL COMPOUND ADEKA CORP (JP) 2019-10-23 EP claimed
JP-2011526957-A 2011-10-20 JP claimed
EP-2307461-A1 POLYMERS FUNCTIONALIZED WITH IMIDE COMPOUNDS CONTAINING A PROTECTED AMINO GROUP Bridgestone Corporation (JP) 2011-04-13 EP claimed
US-20100004414-A1 POLYMERS FUNCTIONALIZED WITH IMIDE COMPOUNDS CONTAINING A PROTECTED AMINO GROUP BRIDGESTONE CORPORATION (JP) 2010-01-07 US claimed
WO-2010002849-A1 POLYMERS FUNCTIONALIZED WITH IMIDE COMPOUNDS CONTAINING A PROTECTED AMINO GROUP BRIDGESTONE CORPORATION (JP) 2010-01-07 WO claimed
US-20240231224-A9 HALOGEN-AND ALIPHATIC-CONTAINING ORGANOTIN PHOTORESISTS AND METHODS THEREOF LAM RESEARCH CORPORATION 2024-07-11 US disclosed
US-20240134274-A1 HALOGEN-AND ALIPHATIC-CONTAINING ORGANOTIN PHOTORESISTS AND METHODS THEREOF LAM RES CORP (US) 2024-04-25 US disclosed
CN-112625054-B Indole ring substituted aminophenol oxygen radical zinc complex and preparation method and application thereof 华东理工大学 2022-10-28 CN disclosed
CN-108558932-B Bis (2-pyridyl) methyl-substituted aminophenoxy magnesium complex and preparation method and application thereof 华东理工大学 2022-10-25 CN disclosed
EP-3442045-B1 ORGANIC PHOTOELECTRIC CONVERSION ELEMENT, AND SOLAR BATTERY MODULE AND SENSOR PROVIDED WITH SAME SUMITOMO CHEMICAL CO (JP) 2022-01-12 EP disclosed
US-11063219-B2 Organic photoelectric conversion element, and solar cell module and sensor provided with the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2021-07-13 US disclosed
CN-112625054-A Indole ring substituted aminophenol oxygen radical zinc complex and preparation method and application thereof 华东理工大学 2021-04-09 CN disclosed
US-5753721-A Process for the photo-polymerisation of cyclic olefins using a thermostable molybdenum or tungsten catalyst CIBA SPECIALTY CHEMICALS CORPORATION (US) 1998-05-19 US disclosed
EP-0531256-B1 Method for preparing glycosides CIBA GEIGY AG (CH) 1997-04-23 EP disclosed
US-5342929-A Direct glycosylation leads to the desired glycosides in high yield and relatively short reaction times using metal complex salts; large amounts of the alpha- or beta-form are often obtained CIBA-GEIGY CORPORATION (US) 1994-08-30 US disclosed
EP-0531256-A1 Method for preparing glycosides CIBA-GEIGY AG (CH) 1993-03-10 EP disclosed
US-4992544-A Intermediates for b-lactam antibiotics and b-lactamase inhibitor UNIVERSITY OF NOTRE DAME DU LAC (US) 1991-02-12 US disclosed
EP-0073559-B1 PROCESS FOR PREPARING DESACETOXYCEPHALOSPORANIC ACID ELI LILLY AND COMPANY (US) 1986-04-02 EP disclosed
EP-0073559-A2 Process for preparing desacetoxycephalosporanic acid ELI LILLY AND COMPANY (US) 1983-03-09 EP disclosed
US-4346219-A Process for preparing desacetoxycephalosporanic acid ELI LILLY AND COMPANY (US) 1982-08-24 US disclosed