SCHEMBL8315504

SCHEMBL8315504

CC(=O)N(C)[Si](C)(C)C(C)(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
SCHEMBL5440165 0.76
SCHEMBL243947 0.73 CHRM2 (0.31)
SCHEMBL5859603 0.72
SCHEMBL449837 0.71 CHRM1 (0.35)
SCHEMBL202677 0.71 LMNA (0.31)
SCHEMBL537585 0.71
SCHEMBL22200161 0.70
SCHEMBL508215 0.70 LMNA (0.36)
SCHEMBL11022125 0.69
SCHEMBL27981313 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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230387464-A1 Nonaqueous Electrolytic Solution and Nonaqueous Electrolytic Solution Battery MU IONIC SOLUTIONS CORPORATION (JP) 2023-11-30 US disclosed
US-20230387464-A1 Nonaqueous Electrolytic Solution and Nonaqueous Electrolytic Solution Battery MU IONIC SOLUTIONS CORPORATION (JP) 2023-11-30 US disclosed
US-20230125746-A1 Nonaqueous Electrolytic Solution and Nonaqueous Electrolytic Solution Battery MITSUBISHI CHEMICAL CORPORATION (JP) 2023-04-27 US disclosed
US-20230125746-A1 Nonaqueous Electrolytic Solution and Nonaqueous Electrolytic Solution Battery MITSUBISHI CHEMICAL CORPORATION (JP) 2023-04-27 US disclosed
EP-4012814-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS-ELECTROLYTIC-SOLUTION BATTERY Mitsubishi Chemical Corporation (JP) 2022-06-15 EP disclosed
WO-2021261579-A1 NONAQUEOUS ELECTROLYTIC SOLUTION AND NONAQUEOUS ELECTROLYTIC SOLUTION BATTERY 三菱ケミカル株式会社 2021-12-30 WO disclosed
EP-0093376-B2 1-Sulfo-2-azetidinone derivatives, their production and use TAKEDA CHEMICAL INDUSTRIES LTD (JP) 1999-04-07 EP disclosed
US-5700920-A SYNTHETIC NUCLEOTIDE COMPRISING BICYCLOHEPTANE OR/AND BICYCLOHEXANE RING; VIRICIDES NOVARTIS CORPORATION (US) 1997-12-23 US disclosed
US-5610300-A ANTIVIRAL, ANTIPROLIFERATIVE, ANTISENSE TECHNOLOGY, DIAGNOSIS CIBA-GEIGY CORPORATION (US) 1997-03-11 US disclosed
US-5461152-A Nucleoside intermediates for antisense oligonucleotides, antiviral agents CIBA-GEIGY CORPORATION (US) 1995-10-24 US disclosed
EP-0083039-B1 4-CYANO-2-AZETIDINONES AND PRODUCTION THEREOF Takeda Chemical Industries, Ltd. (JP) 1986-03-19 EP disclosed
US-4560508-A BETA-LACTAMASE INHIBITORS, ANINICROBIAL AGENT, CHEMICAL INTERMEDIATE TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1985-12-24 US disclosed
US-4550105-A BETA-LACTAMASE INHIBITORS, ANTIBIOTICS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1985-10-29 US disclosed
US-4469794-A Silylation of inorganic oxy-anions THE CURATORS OF THE UNIVERSITY OF MISSOURI (US) 1984-09-04 US disclosed
US-4467037-A Silylation of amino acids THE CURATORS OF THE UNIVERSITY OF MISSOURI (US) 1984-08-21 US disclosed
EP-0100041-A1 1-Sulfo-2-azetidinone derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1984-02-08 EP disclosed
EP-0093376-A2 1-Sulfo-2-azetidinone derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1983-11-09 EP disclosed
EP-0083039-A1 4-Cyano-2-azetidinones and production thereof Takeda Chemical Industries, Ltd. (JP) 1983-07-06 EP disclosed
EP-0053816-A1 1-Sulfo-2-oxoazetidine derivatives, their production and use Takeda Chemical Industries, Ltd. (JP) 1982-06-16 EP disclosed
EP-0053387-A1 Method of preparing 1-sulfo-2-oxoazetidine derivatives and intermediates therefor Takeda Chemical Industries, Ltd. (JP) 1982-06-09 EP disclosed