SCHEMBL2547540

SCHEMBL2547540

NC(=O)OCCOC(N)=O

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 5/20 0.57
TSHR P16473 4/20 0.57
CHRM2 P08172 2/20 0.57
CHRM4 P08173 2/20 0.57
CHRM5 P08912 2/20 0.57
CHRM1 P11229 2/20 0.57
CHRM3 P20309 2/20 0.57
CHRNB2 P17787 2/20 0.57
CHRNA4 P43681 2/20 0.57
CYP2C19 P33261 2/20 0.57
HTR1A P08908 1/20 0.57
CHRNA7 P36544 1/20 0.57
ALOX15 P16050 2/20 0.56
CHRNB4 P30926 1/20 0.48
CHRNA3 P32297 1/20 0.48
HSD17B10 Q99714 3/20 0.39
ALDH1A1 P00352 5/20 0.36
CYP1A2 P05177 2/20 0.36
TDP1 Q9NUW8 2/20 0.36
CYP2D6 P10635 1/20 0.36

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
SCHEMBL30525718 0.96 LMNA (0.62) LMNATSHRCHRM2CHRM4CHRM5
Formaldehyde SCHEMBL4454552 0.93 TSHR (0.52) LMNATSHRCHRM2CHRM4CHRM5
Ethylene SCHEMBL21679941 0.93 TSHR (0.52) LMNATSHRCHRM2CHRM4CHRM5
SCHEMBL30368961 0.90 LMNA (0.50) LMNATSHRCHRM2CHRM4CHRM5
SCHEMBL30552236 0.90 TSHR (0.50) LMNATSHRCHRM2CHRM4CHRM5
SCHEMBL24835739 0.90 TSHR (0.50) LMNATSHRCHRM2CHRM4CHRM5
Ethylene Glycol SCHEMBL722332 0.90 TSHR (0.50) LMNATSHRCHRM2CHRM4CHRM5
SCHEMBL31591142 0.90 TSHR (0.50) LMNATSHRCHRM2CHRM4CHRM5
SCHEMBL5829726 0.87
Ethylene Glycol SCHEMBL9551172 0.87 LMNA (0.48) LMNATSHRCHRM2CHRM4CHRM5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112930487-B Ophthalmic device 鲍希与洛姆伯股份有限公司 2024-07-02 CN claimed
CN-118221944-A Preparation method of acrylic ester modified silicone oil for silicone hydrogel type contact lens 苏州矽合高新材料科技有限公司 2024-06-21 CN claimed
CN-117500873-A High water content biomedical devices 博士伦爱尔兰有限公司 2024-02-02 CN claimed
CN-113956127-B Polymerization inhibitor with high raw material adaptability for extracting and separating carbon five by DMF (dimethyl formamide) method and application thereof 淄博鲁华同方化工有限公司 2022-11-08 CN claimed
EP-2841496-B1 RUBBER COMPOSITIONS ALLNEX GERMANY GMBH (DE) 2022-10-26 EP claimed
CN-110072841-B Method for producing hydroxyethylethylene amines 阿克苏诺贝尔化学品国际有限公司 2022-04-19 CN claimed
CN-110072838-B Process for preparing ethyleneamines 阿克苏诺贝尔化学品国际有限公司 2022-04-15 CN claimed
CN-113979827-A Efficient low-scale polymerization inhibition process for extracting and separating carbon five by DMF (dimethyl formamide) method 淄博鲁华同方化工有限公司 2022-01-28 CN claimed
CN-113956127-A Polymerization inhibitor with high raw material adaptability for extracting and separating carbon five by DMF (dimethyl formamide) method and application thereof 淄博鲁华同方化工有限公司 2022-01-21 CN claimed
CN-113943600-A Lubricant for high-strength cutting steel wire 张家港市耀隆金属制品有限公司 2022-01-18 CN claimed
CN-101511394-A Antimicrobial lenses, processes to prepare them and methods of their use JOHNSON & JOHNSON VISION CARE (US) 2009-08-19 CN claimed
JP-3558134-B2 2004-08-25 JP claimed
US-5869416-A Electrode ink for membrane electrode assembly THE DOW CHEMICAL COMPANY (US) 1999-02-09 US claimed
EP-0853824-A2 FLOW FIELD STRUCTURES FOR MEMBRANE ELECTRODE ASSEMBLIES OF FUEL CELLS THE DOW CHEMICAL COMPANY (US) 1998-07-22 EP claimed
US-5702755-A Process for preparing a membrane/electrode assembly THE DOW CHEMICAL COMPANY (US) 1997-12-30 US claimed
WO-1997013287-A9 FLOW FIELD STRUCTURES FOR MEMBRANE ELECTRODE ASSEMBLIES OF FUEL CELLS 1997-07-03 WO claimed
WO-1997013287-A2 FLOW FIELD STRUCTURES FOR MEMBRANE ELECTRODE ASSEMBLIES OF FUEL CELLS THE DOW CHEMICAL COMPANY (US) 1997-04-10 WO claimed
US-5235007-A Polyepoxides cured by a mixture of diamine and carbamate being the reaction product of a diamine and cyclic carbonate; improved kinetics and mechanical properties TEXACO CHEMICAL COMPANY (US) 1993-08-10 US claimed
EP-0165503-A2 Process for the removal of acid gases from a gas mixture UNION CARBIDE CORPORATION (US) 1985-12-27 EP claimed
US-4171449-A Addition of N,N-dichloro-N-acyl compounds to conjugated dienes and bis-N-chlorocrotyl carbamate products therefrom EXXON RESEARCH & ENGINEERING CO. (US) 1979-10-16 US claimed