SCHEMBL1325071

SCHEMBL1325071

CC(C)C(C)[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
SCHEMBL41781 0.64
SCHEMBL19382324 0.61 ALDH1A1 (0.31)
SCHEMBL5014669 0.60
SCHEMBL231463 0.60
Hydrochloric Acid SCHEMBL7192891 0.60
SCHEMBL5581970 0.57
SCHEMBL9397424 0.57
SCHEMBL10346404 0.57 ALDH1A1 (0.50)
SCHEMBL28659823 0.57
SCHEMBL23671 0.54

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0280962-B1 PROCESS FOR PREPARING 4-ACETOXY-3-HYDROXYETHYLAZETIDIN-2-ONE DERIVATIVES KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1992-05-13 EP claimed
US-4914199-A REACTING PROTECTED BETA-LACTAM WITH ACETIC ANHYDRIDE IN PRESENCE OF BASE AND ACID CATALYST KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1990-04-03 US claimed
EP-0280962-A1 Process for preparing 4-acetoxy-3-hydroxyethylazetidin-2-one derivatives KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1988-09-07 EP claimed
US-8182695-B2 Bridged macrocyclic module compositions WHITEFORD JEFFERY A (US) 2012-05-22 US disclosed
US-8058261-B2 3′-ethynylcytidine derivative TAIHO PHARMACEUTICAL CO., LTD. (JP) 2011-11-15 US disclosed
EP-2045258-B1 3'-ETHYNYLCYTIDINE DERIVATIVE TAIHO PHARMACEUTICAL CO LTD (JP) 2011-09-21 EP disclosed
US-20090306008-A1 3'-ETHYNYLCYTIDINE DERIVATIVE Sasaki, Takuma (JP) 2009-12-10 US disclosed
EP-2045258-A1 3'-ETHYNYLCYTIDINE DERIVATIVE Taiho Pharmaceutical Co., Ltd. (JP) 2009-04-08 EP disclosed
US-20080290034-A1 Bridged macrocyclic module compositions COVALENT PARTNERS LLC 2008-11-27 US disclosed
US-7368564-B2 Bridged macrocyclic module compositions COVALENT PARTNERS, LLC (US) 2008-05-06 US disclosed
EP-1114815-B1 Process to prepare taxol UPJOHN CO (US) 2004-09-29 EP disclosed
US-4914199-A REACTING PROTECTED BETA-LACTAM WITH ACETIC ANHYDRIDE IN PRESENCE OF BASE AND ACID CATALYST KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1990-04-03 US disclosed
US-4892962-A FROM ALLYL DIFLUOROACETATES AND A MONOCHLORO=SILANE, ADDITION POLYMERS CIBA-GEIGY CORPORATION (US) 1990-01-09 US disclosed
US-4806667-A Promoting production of useful livestock with silylated aminophenylethylamine derivatives BAYER AKTIENGESELLSCHAFT (DE) 1989-02-21 US disclosed
EP-0280962-A1 Process for preparing 4-acetoxy-3-hydroxyethylazetidin-2-one derivatives KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1988-09-07 EP disclosed
EP-0247378-A1 Process for preparing 4-acetoxy-3-hydroxyethylazetidin-2-one derivatives KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1987-12-02 EP disclosed
US-4692536-A Process for the preparation of hemiaminals, and the use thereof CIBA-GEIGY CORPORATION (US) 1987-09-08 US disclosed
EP-0009201-B1 SELECTIVELY PROTECTED 4,6-DI-O-(AMINOGLYCOSYL)-1,3-DIAMINOCYCLITOLS, METHOD FOR THEIR PREPARATION AND THEIR USE AS INTERMEDIATES BAYER AG (DE) 1981-12-02 EP disclosed
US-4294959-A Selectively protected 4,6-di-O-(aminoglycosyl)-1,3-diaminocyclitols and their production BAYER AKTIENGESELLSCHAFT (DE) 1981-10-13 US disclosed
EP-0009201-A1 Selectively protected 4,6-di-O-(aminoglycosyl)-1,3-diaminocyclitols, method for their preparation and their use as intermediates BAYER AG (DE) 1980-04-02 EP disclosed