SCHEMBL3432707

SCHEMBL3432707

C=CC[Si](CC=C)(CC=C)C(N)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
SCHEMBL11361565 0.72
SCHEMBL3671706 0.70
SCHEMBL9838352 0.69
SCHEMBL3666532 0.67
SCHEMBL9318653 0.67
SCHEMBL8518166 0.67
SCHEMBL1472599 0.67
SCHEMBL3804318 0.65
SCHEMBL9603578 0.65
SCHEMBL18918479 0.65

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100273696-A1 Composition and method for the prevention and removal of unwanted paint on a surface HOPFSTOCK HERBERT 2010-10-28 US claimed
US-20100273696-A1 Composition and method for the prevention and removal of unwanted paint on a surface HOPFSTOCK HERBERT 2010-10-28 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
US-7087776-B2 Silanol enzyme inhibitors RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 2006-08-08 US disclosed
US-6960678-B2 Silanol enzyme inhibitors THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 2005-11-01 US disclosed
EP-1019533-B1 SILANOL ENZYME INHIBITORS UNIV NEW YORK STATE RES FOUND (US) 2005-09-21 EP disclosed
US-20050171059-A1 Silanol enzyme inhibitors RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK. 2005-08-04 US disclosed
US-20030096793-A1 Inhibit protease enzymes; Benzyl 5-(benzoylamino)-4,4-dihydroxy-7- methyl-4-sila-octanamide, for example can be used to inhibit HIV protease in the treatment of AIDS RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK 2003-05-22 US disclosed
US-6441212-B1 SILANEDIOL TRIMER OR LARGER MOIETY CONTAINING AT LEAST ONE AMINO OR AMIDO GROUP; ISOSTERES THAT ASPARTIC PROTEASES ACT UPON; NOT CLEAVED UNDER ENZYMATIC CONDITIONS; HUMAN IMMUNODEFICIENCY VIRUS RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK 2002-08-27 US disclosed
EP-1019533-A4 SILANOL ENZYME INHIBITORS UNIV NEW YORK STATE RES FOUND (US) 2001-07-25 EP disclosed
EP-1019533-A1 SILANOL ENZYME INHIBITORS THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 2000-07-19 EP disclosed
US-5760019-A INHIBIT PROTEASE ENZYMES THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 1998-06-02 US disclosed
EP-0558047-B1 Copolymer having amino group and process for production thereof DAI ICHI KOGYO SEIYAKU CO LTD (JP) 1998-05-20 EP disclosed
WO-1998002578-A1 SILANOL ENZYME INHIBITORS THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 1998-01-22 WO disclosed
US-5486581-A IODIDE SALTS SHELL OIL COMPANY (US) 1996-01-23 US disclosed
EP-0558047-A2 Copolymer having amino group and process for production thereof DAI-ICHI KOGYO SEIYAKU Co., Ltd. (JP) 1993-09-01 EP disclosed