SCHEMBL2347829

SCHEMBL2347829

C[C](O[SiH](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
SCHEMBL2348005 0.69
SCHEMBL2720438 0.67 ELANE (0.34)
SCHEMBL11192912 0.66
SCHEMBL7718363 0.62
SCHEMBL7715484 0.62
SCHEMBL28747343 0.61 MIF (0.33)
SCHEMBL7057311 0.60
SCHEMBL339422 0.60
Methyl Alcohol SCHEMBL3363304 0.58
SCHEMBL21065525 0.56

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113549102-B Method for removing p-methoxyphenyl protecting group on amide group 凯莱英医药集团(天津)股份有限公司 2021-12-17 CN claimed
CN-113549102-A Method for removing p-methoxyphenyl protecting group on amide group 凯莱英医药集团(天津)股份有限公司 2021-10-26 CN claimed
US-4639441-A ANTIBACTERIAL PENICILLINS SANKYO COMPANY LIMITED (JP) 1987-01-27 US claimed
CN-113549102-B Method for removing p-methoxyphenyl protecting group on amide group 凯莱英医药集团(天津)股份有限公司 2021-12-17 CN disclosed
CN-113549102-A Method for removing p-methoxyphenyl protecting group on amide group 凯莱英医药集团(天津)股份有限公司 2021-10-26 CN disclosed
EP-1489061-B1 PROCESS FOR PRODUCING CYCLIC COMPOUND NIPPON SODA CO (JP) 2011-08-31 EP disclosed
US-7459551-B2 Method for preparing cyclic compounds ASUBIO PHARMA CO., LTD. (JP) 2008-12-02 US disclosed
US-20050209450-A1 Process for producing cyclic compound NIPPON SODA CO., LTD. (JP) 2005-09-22 US disclosed
EP-1489061-A1 PROCESS FOR PRODUCING CYCLIC COMPOUND NIPPON SODA CO., LTD. (JP) 2004-12-22 EP disclosed
EP-0974582-B1 Process for the preparation of 4-substituted azetidinone derivatives TAKASAGO PERFUMERY CO LTD (JP) 2003-02-12 EP disclosed
EP-0597423-B1 Azetidinone compound and process for preparation thereof TANABE SEIYAKU CO (JP) 2002-03-06 EP disclosed
US-4960880-A STEREOSPECIFIC SYNTHESIS OF B-LACTAM INTERMEDIATES SHIONOGI & CO., LTD. (JP) 1990-10-02 US disclosed
US-4923857-A CARBAPENICILLINS FUJISAWA PHARMACEUTICAL COMPANY, LTD. (JP) 1990-05-08 US disclosed
EP-0330108-A1 3-Alkenyl-1-azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid compounds FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1989-08-30 EP disclosed
US-4822787-A 3-pyrrolidinylthio-1-azabicyclo(3.2.0)-hept-2-ene-2-carboxylic acid compounds and antimicrobial activity thereof FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1989-04-18 US disclosed
EP-0308867-A2 Alkenylsilylazetidinone intermediates for carbapenems SHIONOGI SEIYAKU KABUSHIKI KAISHA (JP) 1989-03-29 EP disclosed
US-4771134-A Ring-opening process for preparing azetidinone intermediates FARMITALIA CARLO ERBA S.P.A. (IT) 1988-09-13 US disclosed
EP-0272456-A1 3-Pyrrolidinylthio-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid compounds and processes for the preparation thereof FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1988-06-29 EP disclosed
EP-0188247-A1 Process for preparing azetidinone intermediates FARMITALIA CARLO ERBA S.r.l. (IT) 1986-07-23 EP disclosed
US-4395418-A 6-HYDROXYETHYL SUBSTITUTED ANTIBIOTICS SANKYO COMPANY LIMITED (JP) 1983-07-26 US disclosed