SCHEMBL786977

SCHEMBL786977

CC(C)CC[SiH](C)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
SCHEMBL502601 0.78 LMNA (0.62)
SCHEMBL11494541 0.76 LMNA (0.46)
SCHEMBL475974 0.74 LMNA (0.35)
SCHEMBL12253281 0.71
SCHEMBL17024471 0.69 CA1 (0.33)
SCHEMBL4731998 0.69
SCHEMBL1042475 0.69
SCHEMBL17024470 0.69 CA1 (0.33)
SCHEMBL15091491 0.69
SCHEMBL5069563 0.69

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106146851-A Photocurable composition and comprise its solidfied material 信越化学工业株式会社 2016-11-23 CN disclosed
US-20160199282-A1 PERFORMANCE-ENHANCED HAIR TREATMENT COMPOSITION HENKEL AG & CO. KGAA (DE) 2016-07-14 US disclosed
US-20150166342-A1 Functionalized Matrices for Dispersion of Nanostructures NANOSYS, INC. (US) 2015-06-18 US disclosed
US-20140362335-A1 POLYMER-DOPED VERTICALLY-ALIGNED NEMATIC LIQUID CRYSTALS LC VISION, LLC (US) 2014-12-11 US disclosed
US-8450476-B2 Making drospirenone; chemical intermediates e.g. carbethoxy-drospirenone; industrial scale, safe (no chromium catalyst), meets purity requirements RICHTER GEDEON NYRT. (HU) 2013-05-28 US disclosed
US-20130043433-A1 Functionalized Matrixes for Dispersion of Nanostructures NANOSYS, INC. (US) 2013-02-21 US disclosed
US-8309712-B2 Synthesis of drospirenone in only eight steps; claimed intermediates; readily available raw materials; simple crystallization purification; no hazardous materials; yield RICHTER GEDEON NYRT. (HU) 2012-11-13 US disclosed
US-20120068118-A1 NANOCRYSTAL DOPED MATRIXES SAMSUNG ELECTRONICS CO., LTD. (KR) 2012-03-22 US disclosed
EP-2264124-A1 Polymeric fluorescent substance and polymer light-emitting device using the same Sumitomo Chemical Company, Limited (JP) 2010-12-22 EP disclosed
EP-2221353-A2 New polymeric fluorescent substance and polymer light-emitting device using the same Sumitomo Chemical Company, Limited (JP) 2010-08-25 EP disclosed
US-20020058157-A1 Polymeric fluorescent substance and polymer light-emitting device using the same SUMITOMO CHEMICAL COMPANY, LIMITED 2002-05-16 US disclosed
EP-1205526-A1 Polymeric fluorescent substance and polymer light-emitting device using the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-05-15 EP disclosed
EP-0255278-B1 SYNTHESIS OF AZETIDINONES SCHERING CORPORATION (US) 1992-03-11 EP disclosed
US-5075438-A Synthesis of azetidinones SCHERING CORPORATION (US) 1991-12-24 US disclosed
US-5053502-A Anhydro penicillin derivatives SCHERING CORPORATION (US) 1991-10-01 US disclosed
US-4992591-A Preparation of alpha-(3,4-disubstituted aryl) cyclic ketones SCHERING CORPORATION (US) 1991-02-12 US disclosed
US-4948885-A Synthesis of azetidinones SCHERING-PLOUGH CORP. (US) 1990-08-14 US disclosed
US-4876338-A Synthesis of azetidinones using CuCl SCHERING CORPORATION (US) 1989-10-24 US disclosed
US-4767853-A Synthesis of 1-(allyloxycarbonyl)-methyl-3-(hydroxyethyl)-4-beta-naphthoxythiocarbonylthio-2-azetidinones and hydroxy protected analogs thereof SCHERING CORPORATION (US) 1988-08-30 US disclosed
EP-0255278-A1 Synthesis of azetidinones SCHERING CORPORATION (US) 1988-02-03 EP disclosed