SCHEMBL6565540

SCHEMBL6565540

CCCCCCCCC[Si](C)(C)C

nearest known ligand 0.53

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.53
THRB P10828 1/20 0.53
DNM1 Q05193 7/20 0.40
ALDH1A1 P00352 3/20 0.40
LMNA P02545 2/20 0.40
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
HSD17B10 Q99714 1/20 0.40
SLC22A1 O15245 1/20 0.40
EPHX1 P07099 1/20 0.40

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
SCHEMBL13656438 1.00 TSHR (0.53) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL274817 1.00 TSHR (0.53) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL18079767 1.00 TSHR (0.53) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL28647432 1.00 TSHR (0.53) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL270268 1.00 TSHR (0.53) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL5664939 1.00 TSHR (0.53) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL25241608 1.00 TSHR (0.53) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL3971101 1.00 TSHR (0.53) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL3915336 1.00 TSHR (0.53) TSHRTHRBDNM1ALDH1A1LMNA
SCHEMBL27938627 1.00 TSHR (0.53) 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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240173235-A1 PERSONAL CARE COMPOSITIONS COMPRISING SILAHYDROCARBONS MOMENTIVE PERFORMANCE MATERIALS INC. 2024-05-30 US claimed
EP-4322915-A1 PERSONAL CARE COMPOSITIONS COMPRISING SILAHYDROCARBONS Momentive Performance Materials Inc. (US) 2024-02-21 EP claimed
WO-2022221354-A1 PERSONAL CARE COMPOSITIONS COMPRISING SILAHYDROCARBONS MOMENTIVE PERFORMANCE MATERIALS INC. (US) 2022-10-20 WO claimed
CN-115057994-A Olefin metathesis polymerization method based on diazo monomer and polymer thereof 安徽大学 2022-09-16 CN claimed
CN-110873764-A Method for determining end-capping condition of raw silicone rubber 山东永安胶业有限公司 2020-03-10 CN claimed
CN-108165967-B A kind of metal conditioner 宁波市新光货架有限公司 2019-11-22 CN claimed
CN-108165968-B A kind of metal surface treatment process 宁波市新光货架有限公司 2019-11-22 CN claimed
CN-118459484-A N-type organic molecules with near infrared response and application thereof 广州光达创新科技有限公司 2024-08-09 CN disclosed
WO-2024160042-A1 ORGANIC PHOTOSENSITIVE MOLECULE HAVING SPECTRAL RESPONSE REACHING INFRARED REGION, AND USE THEREOF 广州光达创新科技有限公司 2024-08-08 WO disclosed
CN-115057994-B Olefin metathesis polymerization method based on diazonium monomer and polymer thereof 安徽大学 2024-07-30 CN disclosed
CN-118290445-A Preparation method and application of deuterated quinoid end-capped N-type organic molecules with short-wave infrared response and deuterated quinoid end groups 广州光达创新科技有限公司 2024-07-05 CN disclosed
US-20240173235-A1 PERSONAL CARE COMPOSITIONS COMPRISING SILAHYDROCARBONS MOMENTIVE PERFORMANCE MATERIALS INC. 2024-05-30 US disclosed
EP-4322915-A1 PERSONAL CARE COMPOSITIONS COMPRISING SILAHYDROCARBONS Momentive Performance Materials Inc. (US) 2024-02-21 EP disclosed
CN-213448899-U Metal embedded part for hoisting assembly type concrete prefabricated part 任丘市鑫标汽车配件有限公司 2021-06-15 CN disclosed
CN-110873764-A Method for determining end-capping condition of raw silicone rubber 山东永安胶业有限公司 2020-03-10 CN disclosed
CN-108165967-A A kind of metal conditioner 宁波市新光货架有限公司 2018-06-15 CN disclosed
EP-1032581-B1 CHEMICAL SYNTHESIS OF 6-O-ALKYL ERYTHROMYCIN A ABBOTT LAB (US) 2004-03-31 EP disclosed
EP-1032581-A1 CHEMICAL SYNTHESIS OF 6-O-ALKYL ERYTHROMYCIN A Abbott Laboratories (US) 2000-09-06 EP disclosed
WO-1999025723-A1 CHEMICAL SYNTHESIS OF 6-O-ALKYL ERYTHROMYCIN A ABBOTT LABORATORIES (US) 1999-05-27 WO disclosed
US-5852180-A Chemical synthesis of 6-O-alkyl erythromycin A ABBOTT LABORATORIES (US) 1998-12-22 US disclosed