SCHEMBL12825628

SCHEMBL12825628

C1CCC(P(C2CCCCC2)C2CCCCC2)CC1.Cc1cc(C)c(C2CNC(=C(CC=[Ru-2](Cl)Cl)c3ccccn3)N2c2c(C)cc(C)cc2C)c(C)c1.Cc1ccccc1N1CCN(c2ccccc2C)C1=[Ru-4](Cl)(Cl)=Cc1ccccc1

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
SCHEMBL15621087 0.74
SCHEMBL12814546 0.70 GRM4 (0.32)
SCHEMBL12814320 0.64
Hydrochloric Acid SCHEMBL935838 0.60
SCHEMBL133552 0.60 BACE1 (0.30)
SCHEMBL16699727 0.60 BACE1 (0.30)
SCHEMBL1535715 0.60
Hydrochloric Acid SCHEMBL547963 0.60
SCHEMBL1535723 0.59 BACE1 (0.31)
SCHEMBL4903074 0.59

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2688921-A2 DIBLOCK COPOLYMERS PREPARED BY CROSS METATHESIS Exxonmobil Chemical Patents Inc. (US) 2014-01-29 EP disclosed
EP-2688954-A2 OLEFIN TRIBLOCK POLYMERS VIA RING-OPENING METATHESIS POLYMERIZATION Exxonmobil Chemical Patents Inc. (US) 2014-01-29 EP disclosed
WO-2013158225-A1 POLYOLEFIN COMPOSITIONS AND METHODS OF PRODUCTION THEREOF EXXONMOBIL CHEMICAL PATENTS INC. (US) 2013-10-24 WO disclosed
WO-2012134713-A2 OLEFIN TRIBLOCK POLYMERS VIA RING-OPENING METATHESIS POLYMERIZATION EXXONMOBIL CHEMICAL PATENTS INC. (US) 2012-10-04 WO disclosed
WO-2012134722-A2 DIBLOCK COPOLYMERS PREPARED BY CROSS METATHESIS EXXONMOBIL CHEMICAL PATENTS INC. (US) 2012-10-04 WO disclosed