SCHEMBL4605976

SCHEMBL4605976

CC(C)(CCCC(=O)[O-])C(C)(C)C(=O)[O-].CC(C)(CCCC(=O)[O-])C(C)(C)C(=O)[O-].CC(C)(CCCC(=O)[O-])C(C)(C)C(=O)[O-].[Bi+3].[Bi+3]

nearest known ligand 0.41

Known targets — ChEMBL curated mechanism

HRH2

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
CA1 P00915 3/20 0.41
BBOX1 O75936 5/20 0.39
FFAR3 O14843 2/20 0.36
HDAC3 O15379 2/20 0.36
HDAC1 Q13547 2/20 0.36
HDAC2 Q92769 2/20 0.36
HDAC8 Q9BY41 2/20 0.36
FABP3 P05413 5/20 0.33

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
SCHEMBL1078446 0.96 CA1 (0.41) CA1BBOX1FFAR3HDAC3HDAC1
SCHEMBL28734517 0.96 CA1 (0.41) CA1BBOX1FFAR3HDAC3HDAC1
SCHEMBL28554324 0.96 CA1 (0.41) CA1BBOX1FFAR3HDAC3HDAC1
SCHEMBL28993819 0.96 CA1 (0.41) CA1BBOX1FFAR3HDAC3HDAC1
SCHEMBL28431562 0.96 CA1 (0.41) CA1BBOX1FFAR3HDAC3HDAC1
SCHEMBL3056657 0.96 CA1 (0.41) CA1BBOX1FFAR3HDAC3HDAC1
SCHEMBL3333402 0.96 CA1 (0.41) CA1BBOX1FFAR3HDAC3HDAC1
Silver SCHEMBL3333399 0.96 CA1 (0.41) CA1BBOX1FFAR3HDAC3HDAC1
Lithium Ion SCHEMBL1100575 0.96 CA1 (0.41) CA1BBOX1FFAR3HDAC3HDAC1
SCHEMBL28423097 0.92 CA1 (0.39) CA1BBOX1FFAR3HDAC3HDAC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1943282-B1 PREPARATION OF AMINO-SILANE TERMINATED POLYMER BY USING ORGANIC BISMUTH CATALYST AND CURED POLYMER THEREFROM BY USING NON-TIN CATALYST MOMENTIVE PERFORMANCE MAT INC (US) 2020-03-04 EP claimed
EP-2518094-A1 Preperartion of amino-silane terminated polymer by using organic bismuth catalyst and cured polymer therefrom by using non-tin catalyst Momentive Performance Materials Inc. (US) 2012-10-31 EP claimed
US-8232362-B2 Preparation of amino-silane terminated polymer by using organic bismuth catalyst and cured polymer therefrom by using non-tin catalyst MOMENTIVE PERFORMANCE MATERIALS INC. (US) 2012-07-31 US claimed
EP-1943282-A2 PREPARATION OF AMINO-SILANE TERMINATED POLYMER BY USING ORGANIC BISMUTH CATALYST AND CURED POLYMER THEREFROM BY USING NON-TIN CATALYST Momentive Performance Materials Inc. (US) 2008-07-16 EP claimed
WO-2007037915-A2 PREPARATION OF AMINO-SILANE TERMINATED POLYMER BY USING ORGANIC BISMUTH CATALYST AND CURED POLYMER THEREFROM BY USING NON-TIN CATALYST MOMENTIVE PERFORMANCE MATERIALS INC. (US) 2007-04-05 WO claimed
US-20070060732-A1 Preparation of amino-silane terminated polymer by using organic bismuth catalyst and cured polymer therefrom by using non-tin catalyst MOMENTIVE PERFORMANCE MATERIALS INC. 2007-03-15 US claimed
CN-119875108-B Preparation method of high molecular weight silane modified polyether 浙江皇马科技股份有限公司 2025-06-03 CN disclosed
EP-3719086-B1 ACRYLIC POLYSILOXANE RESIN COATING MATERIAL COMPOSITION AND USE THEREOF CHUGOKU MARINE PAINTS (JP) 2025-05-07 EP disclosed
CN-119875108-A Preparation method of high molecular weight silane modified polyether 浙江皇马科技股份有限公司 2025-04-25 CN disclosed
CN-114829429-B Method for producing organooxysilane-terminated polymers 瓦克化学股份公司 2024-05-14 CN disclosed
WO-2023095636-A1 METHOD FOR PRODUCING HYDROLYZABLE SILYL GROUP-CONTAINING POLYOXYALKYLENE 株式会社カネカ 2023-06-01 WO disclosed
CN-113461902-B Siloxane-terminated polymer homo-polymerization preparation method and moisture-curing composition 娄从江 2023-03-14 CN disclosed
CN-111936557-B Method for producing silane-terminated polymers 瓦克化学股份公司 2023-03-14 CN disclosed
EP-2518094-A1 Preperartion of amino-silane terminated polymer by using organic bismuth catalyst and cured polymer therefrom by using non-tin catalyst Momentive Performance Materials Inc. (US) 2012-10-31 EP disclosed
US-8232362-B2 Preparation of amino-silane terminated polymer by using organic bismuth catalyst and cured polymer therefrom by using non-tin catalyst MOMENTIVE PERFORMANCE MATERIALS INC. (US) 2012-07-31 US disclosed
EP-1943282-A2 PREPARATION OF AMINO-SILANE TERMINATED POLYMER BY USING ORGANIC BISMUTH CATALYST AND CURED POLYMER THEREFROM BY USING NON-TIN CATALYST Momentive Performance Materials Inc. (US) 2008-07-16 EP disclosed
US-7319128-B2 Reacting hydroxy-terminated polysiloxanes with isocyanato-functional silanes in presence of bismuth/zinc carboxylate catalyst; improved moisture/storage stability WACKER CHEMIE AG (DE) 2008-01-15 US disclosed
WO-2007037915-A2 PREPARATION OF AMINO-SILANE TERMINATED POLYMER BY USING ORGANIC BISMUTH CATALYST AND CURED POLYMER THEREFROM BY USING NON-TIN CATALYST MOMENTIVE PERFORMANCE MATERIALS INC. (US) 2007-04-05 WO disclosed
US-20070060732-A1 Preparation of amino-silane terminated polymer by using organic bismuth catalyst and cured polymer therefrom by using non-tin catalyst MOMENTIVE PERFORMANCE MATERIALS INC. 2007-03-15 US disclosed
US-20050119436-A1 Preparation of organyloxysilyl-terminated polymers WACKER-CHEMIE GMBH (DE) 2005-06-02 US disclosed