SCHEMBL4605980

SCHEMBL4605980

COC(=O)C(C)(C)C(C)CCCC(=O)O.[BiH3]

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.41
PLA2G10 O15496 1/20 0.37
ALDH1A1 P00352 1/20 0.36
FOLH1 Q04609 2/20 0.35
GABRP O00591 2/20 0.34
GABRD O14764 2/20 0.34
GABRA1 P14867 2/20 0.34
GABRB1 P18505 2/20 0.34
GABRG2 P18507 2/20 0.34
GABRB3 P28472 2/20 0.34
GABRA5 P31644 2/20 0.34
GABRA3 P34903 2/20 0.34
GABRA2 P47869 2/20 0.34
GABRB2 P47870 2/20 0.34
GABRA4 P48169 2/20 0.34
GABRE P78334 2/20 0.34
GABRA6 Q16445 2/20 0.34
GABRG1 Q8N1C3 2/20 0.34
GABRG3 Q99928 2/20 0.34
GABRQ Q9UN88 2/20 0.34

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
SCHEMBL620277 0.98 TSHR (0.42) TSHRPLA2G10ALDH1A1FOLH1GABRP
SCHEMBL8645646 0.93 TSHR (0.41) TSHRPLA2G10ALDH1A1ENPEPGSTK1
SCHEMBL22190520 0.92 ALDH1A1 (0.43) TSHRPLA2G10ALDH1A1GSTK1SLC22A6
Lithium Ion SCHEMBL1100579 0.81 CA1 (0.38) FOLH1
Silver SCHEMBL3333401 0.81 CA1 (0.38)
SCHEMBL1114582 0.80 CA2 (0.48) LMNA
SCHEMBL9540341 0.80 GABRP (0.40) TSHRALDH1A1FOLH1GABRPGABRD
SCHEMBL22573795 0.79 PRSS1 (0.46) LMNA
SCHEMBL21580900 0.78 TSHR (0.45) TSHRALDH1A1LMNA
SCHEMBL32680456 0.77 ALDH1A1 (0.37) TSHRALDH1A1SLC22A6LMNAFFAR4

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 40 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
US-11555134-B2 Acrylic polysiloxane resin coating compositions and uses thereof CHUGOKU MARINE PAINTS, LTD. (JP) 2023-01-17 US 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