SCHEMBL722324

SCHEMBL722324

C=CC[SiH](N)CC=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
SCHEMBL6255494 0.77
SCHEMBL3507662 0.72
SCHEMBL7749359 0.72
SCHEMBL3368173 0.69
SCHEMBL263285 0.67 TSHR (0.33)
SCHEMBL5758677 0.65
SCHEMBL13490 0.65
SCHEMBL16994735 0.65
SCHEMBL11297781 0.64 TSHR (0.31)
SCHEMBL9427942 0.64 TSHR (0.31)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024147018-A1 SHAPE-CONTROLLED SYNTHESIS OF III-V COLLOIDAL NANOCRYSTALS QUANTUM SCIENCE LTD (GB) 2024-07-11 WO claimed
WO-2024147017-A1 INDIUM MIXED-PNICTOGENIDE QUANTUM DOTS QUANTUM SCIENCE LTD (GB) 2024-07-11 WO claimed
WO-2024147016-A1 METHOD FOR PRODUCING LEAD-FREE NANOCRYSTALS QUANTUM SCIENCE LTD (GB) 2024-07-11 WO claimed
WO-2024147019-A1 SCALABLE SYNTHESIS OF III-V NANOCRYSTALS QUANTUM SCIENCE LTD (GB) 2024-07-11 WO claimed
WO-2024147017-A1 INDIUM MIXED-PNICTOGENIDE QUANTUM DOTS QUANTUM SCIENCE LTD (GB) 2024-07-11 WO disclosed
WO-2024147019-A1 SCALABLE SYNTHESIS OF III-V NANOCRYSTALS QUANTUM SCIENCE LTD (GB) 2024-07-11 WO disclosed
WO-2024147016-A1 METHOD FOR PRODUCING LEAD-FREE NANOCRYSTALS QUANTUM SCIENCE LTD (GB) 2024-07-11 WO disclosed
WO-2024147018-A1 SHAPE-CONTROLLED SYNTHESIS OF III-V COLLOIDAL NANOCRYSTALS QUANTUM SCIENCE LTD (GB) 2024-07-11 WO disclosed
US-8124714-B2 Silicon-urea-azolides, their preparation and use in the preparation of silicones with isocyanate terminal groups 3M INNOVATIVE PROPERTIES COMPANY (US) 2012-02-28 US disclosed
US-20100273696-A1 Composition and method for the prevention and removal of unwanted paint on a surface HOPFSTOCK HERBERT 2010-10-28 US disclosed
EP-1940851-B1 SILICON-UREA-AZOLIDES, THEIR PREPARATION AND USE 3M INNOVATIVE PROPERTIES CO (US) 2010-04-07 EP disclosed
US-20090258999-A1 SILICON-UREA-AZOLIDES, THEIR PREPARATION AND USE IN THE PREPARATION OF SILICONES WITH ISOCYANATE TERMINAL GROUPS 3M INNOVATIVE PROPERTIES COMPANY 2009-10-15 US disclosed
EP-1940851-A2 SILICON-UREA-AZOLIDES, THEIR PREPARATION AND USE 3M Innovative Properties Company (US) 2008-07-09 EP disclosed
WO-2007050950-A2 SILICON-UREA-AZOLIDES, THEIR PREPARATION AND USE IN THE PREPARATION OF SILICONES WITH ISOCYANATE TERMINAL GROUPS 3M INNOVATIVE PROPERTIES COMPANY (US) 2007-05-03 WO disclosed
EP-1780213-A1 Silicon-urea-azolides, their preparation and use in the preparation of silicones with isocyanate terminal groups 3M Innovative Properties Company (US) 2007-05-02 EP disclosed
WO-2000050377-A1 EFFICIENT SYNTHESIS OF SECONDARY AMINES BY SELECTIVE ALKYLATION OF PRIMARY AMINES UNIVERSITY OF SOUTH FLORIDA (US) 2000-08-31 WO disclosed
EP-0564050-B1 Epoxidized diene elastomers for exterior block crosslinking SHELL INT RESEARCH (NL) 1999-08-18 EP disclosed
EP-0564050-A2 Epoxidized diene elastomers for exterior block crosslinking SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1993-10-06 EP disclosed