SCHEMBL686819

SCHEMBL686819

CC(C)(C)N[Si](Cl)(c1ccccc1)c1ccccc1

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ATM Q13315 1/20 0.36
NPC1 O15118 1/20 0.34
RAB9A P51151 1/20 0.34
CCNE2 O96020 2/20 0.33
CDK4 P11802 2/20 0.33
CCND1 P24385 2/20 0.33
CCNE1 P24864 2/20 0.33
CDK2 P24941 2/20 0.33
CCNB2 O95067 1/20 0.33
CDK1 P06493 1/20 0.33
CCNB1 P14635 1/20 0.33
CCNA2 P20248 1/20 0.33
CCNA1 P78396 1/20 0.33
CCNB3 Q8WWL7 1/20 0.33
ESR1 P03372 1/20 0.32
ESR2 Q92731 1/20 0.32
CACNA1F O60840 1/20 0.31
CHRM2 P08172 1/20 0.31
CHRM1 P11229 1/20 0.31
ADRA2B P18089 1/20 0.31

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL6902982 0.82 ESR1 (0.39) ATMNPC1RAB9ACCNE2CDK4
SCHEMBL5694349 0.79 TSHR (0.37) NPC1RAB9A
SCHEMBL11540362 0.78 ATM (0.38) ATMNPC1RAB9ACCNE2CDK4
SCHEMBL7171824 0.77 ACHE (0.41) CYP2D6MAPK1
SCHEMBL6273804 0.76 ESR1 (0.37) ATMNPC1RAB9ACCNE2CDK4
SCHEMBL2101836 0.75 KCNN4 (0.39) ATMESR1ESR2LMNACYP2D6
SCHEMBL2103096 0.71 KCNN4 (0.41) NPC1RAB9AESR1ESR2SLC6A3
SCHEMBL5694351 0.71 ACHE (0.36)
SCHEMBL450654 0.70 TAAR1 (0.36) ATMESR1ESR2LMNACYP2D6
SCHEMBL4241 0.70 ESR1 (0.34) ATMESR1ESR2LMNAMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1242471-B1 SUBSTITUTED GROUP 4 METAL COMPLEXES, CATALYSTS AND OLEFIN POLYMERIZATION PROCESS DOW GLOBAL TECHNOLOGIES LLC (US) 2012-02-29 EP disclosed
EP-1487886-B1 SUBSTITUTED INDENYL METAL COMPLEXES AND POLYMERIZATION PROCESS DOW GLOBAL TECHNOLOGIES INC (US) 2008-08-06 EP disclosed
EP-1487886-A1 SUBSTITUTED INDENYL METAL COMPLEXES AND POLYMERIZATION PROCESS Dow Global Technologies Inc. (US) 2004-12-22 EP disclosed
WO-2003078483-A1 SUBSTITUTED INDENYL METAL COMPLEXES AND POLYMERIZATION PROCESS DOW GLOBAL TECHNOLOGIES INC. (US) 2003-09-25 WO disclosed
US-6515155-B1 Group 4 metal complexes of the constrained geometry type, catalysts derived therefrom and polymerization processes using the same, characterized by a nitrogen containing aliphatic or cycloaliphatic moiety that is substituted with one or more DOW GLOBAL TECHNOLOGIES INC. 2003-02-04 US disclosed
EP-1242471-A1 SUBSTITUTED GROUP 4 METAL COMPLEXES, CATALYSTS AND OLEFIN POLYMERIZATION PROCESS THE DOW CHEMICAL COMPANY (US) 2002-09-25 EP disclosed
WO-2001042315-A1 SUBSTITUTED GROUP 4 METAL COMPLEXES, CATALYSTS AND OLEFIN POLYMERIZATION PROCESS DOW GLOBAL TECHNOLOGIES INC. (US) 2001-06-14 WO disclosed
EP-0563365-B1 PREPARATION OF METAL COORDINATION COMPLEX DOW CHEMICAL CO (US) 1997-11-05 EP disclosed
EP-0781288-A1 METAL COMPLEXES CONTAINING NON-AROMATIC, ANIONIC, DIENYL GROUPS AND ADDITION POLYMERIZATION CATALYSTS THEREFROM THE DOW CHEMICAL COMPANY (US) 1997-07-02 EP disclosed
US-5541349-A COORDINATION CATALYST COMPLEXES OF GROUP 4 METALS IN THE +2 OR +4 OXIDATION STATE AND BOUND TO CYCLIC, NONCYCLIC, NONAROMATIC, ANIONIC OR DIENYL GROUPS; STABILITY THE DOW CHEMICAL COMPANY (US) 1996-07-30 US disclosed
WO-1996008498-A1 METAL COMPLEXES CONTAINING NON-AROMATIC, ANIONIC, DIENYL GROUPS AND ADDITION POLYMERIZATION CATALYSTS THEREFROM THE DOW CHEMICAL COMPANY (US) 1996-03-21 WO disclosed
EP-0563365-A1 PREPARATION OF METAL COORDINATION COMPLEX THE DOW CHEMICAL COMPANY (US) 1993-10-06 EP disclosed
WO-1993008199-A1 PREPARATION OF METAL COORDINATION COMPLEX THE DOW CHEMICAL COMPANY (US) 1993-04-29 WO disclosed