SCHEMBL4581361

SCHEMBL4581361

C=CC1C(C=C)C(C=C)C1C=C

nearest known ligand 0.31

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 1/20 0.31
TSHR P16473 2/20 0.31
ALDH1A1 P00352 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
SCHEMBL14954652 0.69
SCHEMBL31398605 0.69
SCHEMBL3186182 0.59
SCHEMBL7692965 0.59
SCHEMBL7691914 0.59
SCHEMBL1235562 0.59
SCHEMBL8864140 0.58
Hydrochloric Acid SCHEMBL10323675 0.56
Hydrochloric Acid SCHEMBL6931777 0.56
Hydrochloric Acid SCHEMBL31151855 0.54

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 44 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102548632-B To the method for liquid degassing WACKER CHEMIE AG (DE) 2015-09-02 CN disclosed
EP-2485824-B1 METHOD FOR DEAERATING LIQUIDS WACKER CHEMIE AG (DE) 2015-03-04 EP disclosed
US-20120208952-A1 Method for Deaerating Liquids WACKER CHEMIE AG (DE) 2012-08-16 US disclosed
EP-1809232-B1 HAIR CARE COMPOSITIONS UNILEVER PLC (GB) 2012-08-08 EP disclosed
US-20080276836-A1 Composition containing anti-misting component of reduced molecular weight and viscosity MOMENTIVE PERFORMANCE MATERIALS INC. 2008-11-13 US disclosed
US-20080281055-A1 Branched polysiloxane of reduced molecular weight and viscosity MOMENTIVE PERFORMANCE MATERIALS INC. 2008-11-13 US disclosed
EP-1809232-A1 HAIR CARE COMPOSITIONS Unilever PLC (GB) 2007-07-25 EP disclosed
US-7153913-B2 Siloxane polymers containing Si-bound hydrogen atoms as antimisting additives for silicone coating compositons WACKER CHEMIE AG (DE) 2006-12-26 US disclosed
US-7153912-B2 use of branched, alkenyl-functional organopolysiloxanes made by reacting an 1,2,4-trivinylcyclohexane with an organopolysiloxane having Si-bonded hydrogen atoms, using a hydrosilylation catalyst; use in high speed coating of substrates such as paper WACKER CHEMIE AG (DE) 2006-12-26 US disclosed
EP-1481018-B1 SILOXANE POLYMERS CONTAINING SI-BOUND HYDROGEN ATOMS AS ANTIMISTING ADDITIVES FOR SILICONE COATING COMPOSITIONS WACKER CHEMIE AG (DE) 2006-11-29 EP disclosed
US-6265497-B1 REACTING AN UNSATURATED COMPOUND WITH POLYSILOXANE WACKER-CHEMIE GMBH (DE) 2001-07-24 US disclosed
EP-1108739-A1 Multiphase compositions of organosilicon compounds Wacker-Chemie GmbH (DE) 2001-06-20 EP disclosed
EP-1008615-A1 Alkenyl group containing siloxane copolymers Wacker-Chemie GmbH (DE) 2000-06-14 EP disclosed
US-5719248-A Siloxane copolymers containing vinyloxy groups, their preparation and their use WACKER-CHEMIE GMBH (DE) 1998-02-17 US disclosed
EP-0523660-B1 Alkenyl group containing siloxane copolymers, their preparation and their use WACKER CHEMIE GMBH (DE) 1997-03-05 EP disclosed
EP-0639206-B1 SILOXANE COPOLYMERS HAVING VINYLOXY GROUPS, THEIR PREPARATION AND USE WACKER CHEMIE GMBH (DE) 1996-02-07 EP disclosed
EP-0639206-A1 SILOXANE COPOLYMERS HAVING VINYLOXY GROUPS, THEIR PREPARATION AND USE. WACKER CHEMIE GMBH (DE) 1995-02-22 EP disclosed
WO-1993022369-A1 SILOXANE COPOLYMERS HAVING VINYLOXY GROUPS, THEIR PREPARATION AND USE WACKER-CHEMIE GMBH (DE) 1993-11-11 WO disclosed
US-5241034-A From polysiloxane containing Si-bonded hydrogen and hydrocarbon with at least two alkenyl groups; for nonstick coatings WACKER-CHEMIE GMBH (DE) 1993-08-31 US disclosed
EP-0523660-A1 Alkenyl group containing siloxane copolymers, their preparation and their use WACKER-CHEMIE GMBH (DE) 1993-01-20 EP disclosed