SCHEMBL6140710

SCHEMBL6140710

O=S(=O)([O-])c1ccccc1.c1cc(OCc2ccncc2)cc([S+](c2cccc(OCc3ccncc3)c2)c2cccc(OCc3ccncc3)c2)c1

nearest known ligand 0.46

Known targets — ChEMBL curated mechanism

CHRNA1CHRNB1CHRNDCHRNECHRNG

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TLR4 O00206 1/20 0.46
TLR2 O60603 1/20 0.46
F2 P00734 5/20 0.45
NOS3 P29474 1/20 0.43
NOS1 P29475 1/20 0.43
NOS2 P35228 1/20 0.43
GPR132 Q9UNW8 1/20 0.43
LMNA P02545 1/20 0.42
MAOB P27338 4/20 0.41
CA12 O43570 1/20 0.41
CA1 P00915 1/20 0.41
CA2 P00918 1/20 0.41
CA4 P22748 1/20 0.41
CA5A P35218 1/20 0.41
CA7 P43166 1/20 0.41
CA9 Q16790 1/20 0.41
CA5B Q9Y2D0 1/20 0.41
SMN1; SMN2 Q16637 2/20 0.40
MEN1 O00255 1/20 0.40
MAPK1 P28482 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
SCHEMBL6140191 0.91 NOS3 (0.49) TLR4TLR2F2NOS3NOS1
SCHEMBL6139950 0.90 NOS3 (0.43) TLR4TLR2F2NOS3NOS1
SCHEMBL6140063 0.89 NOS3 (0.38) TLR4TLR2F2NOS3NOS1
SCHEMBL6140165 0.83 PTPN1 (0.40) F2GPR132LMNAMAOBSMN1; SMN2
SCHEMBL6140456 0.83 TLR4 (0.47) TLR4TLR2GPR132SMN1; SMN2MEN1
SCHEMBL6140802 0.81 NOS3 (0.41) TLR4TLR2F2NOS3NOS1
SCHEMBL6140433 0.81 NOS3 (0.41) TLR4TLR2F2NOS3NOS1
SCHEMBL6140453 0.81 NOS3 (0.45) TLR4TLR2F2NOS3NOS1
SCHEMBL6140818 0.78 CA12 (0.42) F2LMNACA12CA1CA2
SCHEMBL6140338 0.78 RORC (0.41) TLR4TLR2F2NOS3NOS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6955939-B1 Memory element formation with photosensitive polymer dielectric ADVANCED MICRO DEVICES, INC. (US) 2005-10-18 US disclosed
US-6878961-B2 Photosensitive polymeric memory elements ADVANCED MICRO DEVICES, INC. (US) 2005-04-12 US disclosed
US-20050045877-A1 PHOTOSENSITIVE POLYMERIC MEMORY ELEMENTS MORGAN STANLEY SENIOR FUNDING, INC. 2005-03-03 US disclosed
US-6825060-B1 Photosensitive polymeric memory elements ADVANCED MICRO DEVICES, INC. 2004-11-30 US disclosed
US-6534243-B1 A coating containing a cleaving compound to trim resist features; permitting a deprotection region to form within an inner portion of the patterned resist; removing coating and deprotection region to provide a second patterned feature ADVANCED MICRO DEVICES, INC. 2003-03-18 US disclosed
US-6492075-B1 COATING WITH CLEAVING COMPOUND TO CONTROLLABLY DECREASE SIZE OF DEVELOPED RESIST ADVANCED MICRO DEVICES, INC. 2002-12-10 US disclosed
US-6274289-B1 Chemical resist thickness reduction process ADVANCED MICRO DEVICES, INC. 2001-08-14 US disclosed
US-5847218-A Sulfonium salts and chemically amplified positive resist compositions SHIN-ETSU CHEMICAL CO., LTD. (JP) 1998-12-08 US disclosed