SCHEMBL4813310

SCHEMBL4813310

CCCP1(=O)CCCCC1

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
SCHEMBL4808270 1.00
SCHEMBL3272247 0.97
SCHEMBL4811432 0.92
SCHEMBL4816082 0.84 CYP1A2 (0.31)
SCHEMBL10633893 0.82 TDP1 (0.32)
SCHEMBL1107384 0.81 LMNA (0.30)
SCHEMBL4805907 0.80 TSHR (0.36)
SCHEMBL4817998 0.80 TSHR (0.36)
SCHEMBL4815804 0.80 TSHR (0.36)
SCHEMBL10766944 0.79 TSHR (0.33)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9505859-B2 Process for producing polydienes BRIDGESTONE CORPORATION (JP) 2016-11-29 US disclosed
EP-2780381-B1 PROCESS FOR PRODUCING POLYDIENES BRIDGESTONE CORP (JP) 2015-10-07 EP disclosed
US-20140303327-A1 Process For Producing Polydienes BRIDGESTONE CORPORATION (JP) 2014-10-09 US disclosed
EP-2780381-A1 PROCESS FOR PRODUCING POLYDIENES Bridgestone Corporation (JP) 2014-09-24 EP disclosed
WO-2013075085-A1 PROCESS FOR PRODUCING POLYDIENES BRIDGESTONE CORPORATION (JP) 2013-05-23 WO disclosed
US-8323839-B2 rechargeable batteries having a negative electrode comprising a thin film of active material which can absorb and discharge lithium, deposited on current collectors, a positive electrode which can lithiate or delithiate and a sufur or phosphorus compound as an electrolyte; high energy density SANYO ELECTRIC CO., LTD. (JP) 2012-12-04 US disclosed
US-7411096-B2 Process for producing optically active phosphorus heterocyclic dimer NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2008-08-12 US disclosed
US-20060211888-A1 2,2'-bis-(1-alkylphosphetanes); a primary alkyl or cycloalkyl phosphine is reacted with 1,3-dichloropropane, in the presence of n-butyllithium, and then reacted with boron trihydride, oxygen, or sulfur, dimerizing, removing the boron trihydride, oxygen, or sulfur; assymetric hydrogenation catalysts NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2006-09-21 US disclosed
EP-1650216-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE DIMER OF PHOSPHORUS HETEROCYCLE NIPPON CHEMICAL INDUSTRIAL COMPANY LIMITED (JP) 2006-04-26 EP disclosed
US-20060024587-A1 Nonaqueous electrolyte solution for secondary battery and nonaqueous electrolyte secondary battery SANYO ELECTRIC CO., LTD. (JP) 2006-02-02 US disclosed