SCHEMBL3851055

SCHEMBL3851055

C=C(C)CO[Si](C)(C)Cl

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
SCHEMBL7112938 0.81
SCHEMBL160479 0.78
SCHEMBL5030081 0.78 HSD17B10 (0.33)
SCHEMBL9798616 0.75 HSD17B10 (0.35)
SCHEMBL3400816 0.74 HSD17B10 (0.30)
SCHEMBL9798624 0.72
SCHEMBL2200164 0.72
SCHEMBL5009656 0.72 HSD17B10 (0.31)
SCHEMBL4906693 0.70
SCHEMBL6037451 0.70 HSD17B10 (0.33)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240409563-A1 HIGH PURITY POLYSILOXANE MACROMERS AND METHOD FOR MAKING THE SAME GELEST, INC. 2024-12-12 US disclosed
EP-4448536-A1 HIGH PURITY POLYSILOXANE MACROMERS AND METHOD FOR MAKING THE SAME GELEST, INC. (US) 2024-10-23 EP disclosed
CN-118401532-A High-purity polysiloxane macromer and preparation method thereof 盖列斯特有限公司 2024-07-26 CN disclosed
WO-2023113779-A1 HIGH PURITY POLYSILOXANE MACROMERS AND METHOD FOR MAKING THE SAME GELEST, INC. (US) 2023-06-22 WO disclosed
US-20230183273-A1 HIGH PURITY POLYSILOXANE MACROMERS AND METHOD FOR MAKING THE SAME GELEST, INC. 2023-06-15 US disclosed
US-9080017-B2 Siloxane-based composition and cured product thereof, and use therefor CENTRAL GLASS COMPANY, LIMITED (JP) 2015-07-14 US disclosed
US-20140275445-A1 Siloxane-Based Composition and Cured Product Thereof, and Use Therefor CENTRAL GLASS COMPANY, LIMITED (JP) 2014-09-18 US disclosed
US-7576169-B2 Reaction of a silica source derived from combusted organic material such as rice hull ash or pyrolysis by-products with a quaternary ammonium hydroxide compound in alcholic solvent; salt formation, quaternization; stabilization of wood THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2009-08-18 US disclosed
EP-1675671-A2 FACILE SYNTHESIS OF POLYHEDRAL SILSESQUIOXANE ANIONS AND USE THEREOF Regents of the University of Michigan (US) 2006-07-05 EP disclosed
US-20050142054-A1 Facile synthesis of polyhedral silsesquioxane anions and use thereof REGENTS OF THE UNIVERSITY OF MICHIGAN, THE 2005-06-30 US disclosed
WO-2005039744-A2 FACILE SYNTHESIS OF POLYHEDRAL SILSESQUIOXANE ANIONS AND USE THEREOF THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2005-05-06 WO disclosed
US-6197988-B1 DECOMPOSITION IN PRESENCE OF LEWIS ACID METAL HALIDE DOW CORNING TORAY SILICONE CO., LTD. (JP) 2001-03-06 US disclosed
US-5847178-A Method for purifying 3-methacryloxypropyldimethylhalosilanes and 3-methacryloxypropylmethyldihalosilanes DOW CORNING TORAY SILICONE CO., LTD. (JP) 1998-12-08 US disclosed
US-5811565-A TREATING MIXTURE WITH LEWIS ACID HALIDE DOW CORNING TORAY SILICONE CO., LTD. (JP) 1998-09-22 US disclosed