SCHEMBL7679958

SCHEMBL7679958

CC1=C(C)C(C)C([Ti](C)(C)NC2CCCCCCCCCCC2)=C1C.[SiH4]

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
SCHEMBL7622820 0.74 HDAC8 (0.36)
SCHEMBL2365451 0.74 NPC1 (0.32)
SCHEMBL5822648 0.74 NPC1 (0.32)
Biphenyl SCHEMBL7653656 0.71 KMT2A (0.33)
Biphenyl SCHEMBL7653450 0.71 KMT2A (0.33)
Biphenyl SCHEMBL7649341 0.71 KMT2A (0.33)
Biphenyl SCHEMBL7650529 0.71 KMT2A (0.33)
Biphenyl SCHEMBL7653512 0.71 KMT2A (0.33)
Biphenyl SCHEMBL7652147 0.69 MEN1 (0.34)
Hydrochloric Acid SCHEMBL7640397 0.67

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1259556-A2 IMPROVED SILANE FUNCTIONALIZED OLEFIN INTERPOLYMERS AND DERIVATIVES THEREOF THE DOW CHEMICAL COMPANY (US) 2002-11-27 EP disclosed
WO-2001009207-A2 IMPROVED SILANE FUNCTIONALIZED OLEFIN INTERPOLYMERS AND DERIVATIVES THEREOF THE DOW CHEMICAL COMPANY (US) 2001-02-08 WO disclosed