SCHEMBL3034328

SCHEMBL3034328

CCP(CC)CC.CCP(CC)CC.CCP(CC)CC.CCP(CC)CC.[Pd]

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
SCHEMBL4109649 1.00
SCHEMBL3923465 1.00
SCHEMBL1195610 1.00
SCHEMBL41401 0.94
SCHEMBL5409330 0.94
SCHEMBL23495442 0.89
SCHEMBL1985723 0.89
Bromide SCHEMBL6722331 0.89
Phosphine SCHEMBL22589046 0.89
SCHEMBL11677028 0.89

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-2638010-B1 METHOD FOR PREPARING 2,2-DIFLUOROETHYLAMINE DERIVATIVES STARTING FROM N-(2,2-DIFLUOROETHYL)PROP-2-EN-1-AMINE BAYER IP GMBH (DE) 2014-12-31 EP claimed
EP-2638001-B1 METHOD FOR PRODUCING 2,2-DIFLUOROETHYLAMINE BASED ON PROP-2-EN-1-AMINE BAYER IP GMBH (DE) 2014-07-02 EP claimed
US-8766012-B2 Process for the preparation of 2,2-difluoroethylamine starting from prop-2-en-1-amine BAYER CROPSCIENCE AG (DE) 2014-07-01 US claimed
US-8586756-B2 Process for the preparation of 2,2-difluoroethylamine derivatives starting from N-(2,2-difluoroethyl)prop-2-en-1-amine BAYER CROPSCIENCE AG (DE) 2013-11-19 US claimed
US-20120142971-A1 PROCESS FOR THE PREPARATION OF 2,2-DIFLUOROETHYLAMINE STARTING FROM PROP-2-EN-1-AMINE BAYER CROPSCIENCE AG (DE) 2012-06-07 US claimed
US-20120123130-A1 PROCESS FOR THE PREPARATION OF 2,2-DIFLUOROETHYLAMINE DERIVATIVES STARTING FROM N-(2,2-DIFLUOROETHYL)PROP-2-EN-1-AMINE BAYER CROPSCIENCE AG (DE) 2012-05-17 US claimed
US-20100204463-A1 Preparation Of Synthetic Nucleosides via Pi-Allyl Transition Metal Complex Formation EMORY UNIVERSITY 2010-08-12 US claimed
EP-2185508-A1 PREPARATION OF SYNTHETIC NUCLEOSIDES VIA pi-ALLYL TRANSITION METAL COMPLEX FORMATION Emory University (US) 2010-05-19 EP claimed
WO-2009021114-A1 PREPARATION OF SYNTHETIC NUCLEOSIDES VIA π-ALLYL TRANSITION METAL COMPLEX FORMATION EMORY UNIVERSITY (US) 2009-02-12 WO claimed
US-4101566-A Oxidative addition production of trans-halo-2(1,3-alkadienyl)bis(triethylphosphine) complexes of nickel(II), palladium(II), and platinum(II) PHILLIPS PETROLEUM COMPANY (US) 1978-07-18 US claimed
JP-55087728-A None JP disclosed
CN-110204558-B Synthesis of cephalosporin compounds 默沙东公司 2022-05-06 CN disclosed
US-11059835-B2 Synthesis of cephalosporin compounds MERCK SHARP & DOHME CORP. (US) 2021-07-13 US disclosed
US-20200385404-A1 SYNTHESIS OF CEPHALOSPORIN COMPOUNDS MERCK SHARP & DOHME CORP. (US) 2020-12-10 US disclosed
EP-2638010-B1 METHOD FOR PREPARING 2,2-DIFLUOROETHYLAMINE DERIVATIVES STARTING FROM N-(2,2-DIFLUOROETHYL)PROP-2-EN-1-AMINE BAYER IP GMBH (DE) 2014-12-31 EP disclosed
US-20100087643-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE 2-ARYLPIPERAZINE DERIVATIVE KANEKA CORPORATION (JP) 2010-04-08 US disclosed
EP-2119709-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE 2-ARYLPIPERAZINE DERIVATIVE Kaneka Corporation (JP) 2009-11-18 EP disclosed
WO-2009021114-A1 PREPARATION OF SYNTHETIC NUCLEOSIDES VIA π-ALLYL TRANSITION METAL COMPLEX FORMATION EMORY UNIVERSITY (US) 2009-02-12 WO disclosed
US-4230719-A Novel 2-[4-(3-methyl-2-thienyl)phenyl]propionic acid and pharmaceutically acceptable salt thereof and method for treating symptoms of inflammation and pain TOYAMA CHEMICAL CO., LTD. (JP) 1980-10-28 US disclosed
JP-S5587728-A PREPARATION OF 5-ALKENYLNORBORNENE-2 MITSUBISHI PETROCHEM CO LTD 1980-07-02 JP disclosed