SCHEMBL4906320

SCHEMBL4906320

CCC[N+]12CCC(CC1)CC2

nearest known ligand 0.56

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
CHRNA7 P36544 2/20 0.41
LMNA P02545 1/20 0.36
CHRNB2 P17787 1/20 0.32
CHRNB4 P30926 1/20 0.32
CHRNA3 P32297 1/20 0.32
CHRNA4 P43681 1/20 0.32
CHRNA10 Q9GZZ6 1/20 0.32
CHRNA9 Q9UGM1 1/20 0.32
BCHE P06276 1/20 0.31
ACHE P22303 1/20 0.31
CHKA P35790 1/20 0.31

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
SCHEMBL4893867 0.84 APOBEC3A (0.39) CHRNA7CHRNB2CHRNB4CHRNA3CHRNA4
SCHEMBL868069 0.80 GNAI3 (0.41) CHRNA7
SCHEMBL2525998 0.80 GNAI3 (0.41) CHRNA7
Water SCHEMBL2526562 0.79 GNAI3 (0.40) CHRNA7
Iodide SCHEMBL3854066 0.79 GNAI3 (0.40) CHRNA7CHRNB2CHRNB4CHRNA3CHRNA4
Bromide SCHEMBL2524389 0.79 GNAI3 (0.40) CHRNA7BCHEACHE
SCHEMBL4902669 0.77 CHRNA7 (0.45) CHRNA7LMNABCHEACHECHKA
SCHEMBL12638606 0.74 CHRNA7 (0.36) CHRNA7CHRNB2CHRNB4CHRNA3CHRNA4
Bromide SCHEMBL7629729 0.74 CHRNA7 (0.36) CHRNA7CHRNB2CHRNB4CHRNA3CHRNA4
SCHEMBL1666073 0.74 CHRNA7 (0.36) CHRNA7CHRNB2CHRNB4CHRNA3CHRNA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110087729-B Bifunctional compound with quaternary ammonium salt structure 北京硕佰医药科技有限责任公司 2022-04-05 CN claimed
CN-110087729-B Bifunctional compound with quaternary ammonium salt structure 北京硕佰医药科技有限责任公司 2022-04-05 CN disclosed
EP-3556435-A1 CLASS OF BIFUNCTIONAL COMPOUNDS WITH QUATERNARY AMMONIUM SALT STRUCTURE Beijing Showby Pharmaceutical Co., Ltd. (CN) 2019-10-23 EP disclosed
EP-3248982-A1 THIOSULFONATE REAGENTS FOR THE SYNTHESIS OF FUNCTIONALIZED NUCLEIC ACIDS Wave Life Sciences Ltd. (SG) 2017-11-29 EP disclosed
US-9605019-B2 Methods for the synthesis of functionalized nucleic acids WAVE LIFE SCIENCES LTD. (SG) 2017-03-28 US disclosed
EP-2734208-B1 METHODS FOR THE SYNTHESIS OF FUNCTIONALIZED NUCLEIC ACIDS WAVE LIFE SCIENCES LTD (SG) 2017-03-01 EP disclosed
US-20170037399-A1 CHIRAL DESIGN WAVE LIFE SCIENCES LTD. (SG) 2017-02-09 US disclosed
WO-2013012758-A1 METHODS FOR THE SYNTHESIS OF FUNCTIONALIZED NUCLEIC ACIDS ONTORII, INC. (US) 2013-01-24 WO disclosed
EP-1867667-B1 Method for manufacturing stabilized polyacetal resin POLYPLASTICS CO (JP) 2012-10-31 EP disclosed
WO-2008142560-A2 METHOD FOR THE PRODUCTION OF BINARY CLATHRATE HYDRATES OF HYDROGEN ARCA SIMONE (IT) 2008-11-27 WO disclosed
US-20080271381-A1 Method for manufacturing stabilized polyacetal resin, stabilized polyacetal resin, stabilized polyacetal resin composition, and molded article of stabilized polyacetal resin POLYPLASTICS CO., LTD (JP) 2008-11-06 US disclosed
EP-1867667-A1 Method for manufacturing stabilized polyacetal resin, stabilized polyacetal resin, stabilized polyacetal resin composition, and molded article of stabilized polyacetal resin Polyplastics Co., Ltd. (JP) 2007-12-19 EP disclosed