SCHEMBL8328620

SCHEMBL8328620

CCCCCCCC[Sn](I)(I)CCCCCCCC

nearest known ligand 0.50

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.50
THRB P10828 1/20 0.50
DNM1 Q05193 7/20 0.38
ALDH1A1 P00352 3/20 0.38
LMNA P02545 2/20 0.38
MEN1 O00255 2/20 0.38
KMT2A Q03164 2/20 0.38
HSD17B10 Q99714 1/20 0.38
SLC22A1 O15245 1/20 0.38
EPHX1 P07099 1/20 0.38

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
SCHEMBL7782639 1.00 TSHR (0.50) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL7782626 1.00 TSHR (0.50) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL11529424 0.81 TSHR (0.50) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL7777575 0.81 TSHR (0.50) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL8330988 0.81 TSHR (0.50) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL10778431 0.81 TSHR (0.50) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL11529690 0.81 TSHR (0.50) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL11688003 0.79 TSHR (0.47) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL1023945 0.73 TSHR (0.57) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL2554244 0.73 TSHR (0.57) TSHRTHRBDNM1ALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105461746-A Method for preparing dioctyl tin oxide VITAL MAT CO LTD 2016-04-06 CN disclosed
EP-0951359-A1 PROCESS FOR THE REACTIVATION OF IODINE-CONTAINING CATALYSTS EASTMAN CHEMICAL COMPANY (US) 1999-10-27 EP disclosed
WO-1998008604-A1 PROCESS FOR THE REACTIVATION OF IODINE-CONTAINING CATALYSTS EASTMAN CHEMICAL COMPANY (US) 1998-03-05 WO disclosed
US-5693833-A IODINATION WITH AQUEOUS HYDROGEN IODIDE IN THE CATALYTIC ISOMERIZATION EASTMAN CHEMICAL COMPANY (US) 1997-12-02 US disclosed
EP-0496278-B1 Optical device and apparatus using the optical device HAMAMATSU PHOTONICS KK (JP) 1996-10-30 EP disclosed
EP-0412759-B1 Heat-curable type resinous composition and moulded article prepared therefrom NIPPON PAINT CO LTD (JP) 1996-05-08 EP disclosed
EP-0342064-B1 A thermosetting resinous composition and preparation of heat resisting coating and molded product using said composition NIPPON PAINT CO LTD (JP) 1995-02-15 EP disclosed
US-5311350-A Optical device and apparatus using the optical device HAMAMATSU PHOTONICS K.K. (JP) 1994-05-10 US disclosed
US-5200540-A REFINING PROCESS OF ORGANIC TIN (IV) POLYHALIDES KORIYAMA KASEI CO., LTD. (JP) 1993-04-06 US disclosed
EP-0496278-A2 Optical device and apparatus using the optical device HAMAMATSU PHOTONICS K.K. (JP) 1992-07-29 EP disclosed
US-5126423-A Forming heat-resistant moldings of polyoxazolidones; catalyst selectivity NIPPON PAINT CO., LTD. (JP) 1992-06-30 US disclosed
US-5086152-A Complex of organs antimory halide and zinc ralide as catalyst NIPPON PAINT CO., LTD. (JP) 1992-02-04 US disclosed
EP-0412759-A2 Heat-curable type resinous composition and moulded article prepared therefrom NIPPON PAINT CO., LTD. (JP) 1991-02-13 EP disclosed
US-4968823-A CONTINUAL BASIC HYDROLYSIS OF ALKYLTIN HALIDE YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD. (JP) 1990-11-06 US disclosed
EP-0346506-A1 Process for the fractional production of organotin compounds Yoshitomi Pharmaceutical Industries, Ltd. (JP) 1989-12-20 EP disclosed
EP-0342064-A2 A thermosetting resinous composition and preparation of heat resisting coating and molded product using said composition NIPPON PAINT CO., LTD. (JP) 1989-11-15 EP disclosed
US-4148814-A Process for preparing monohydrocarbyltin trihalides PENNWALT CORPORATION (US) 1979-04-10 US disclosed