SCHEMBL6140456

SCHEMBL6140456

O=S(=O)([O-])c1ccccc1.c1ccc(COc2cccc([S+](c3cccc(OCc4ccccn4)c3)c3cccc(OCc4ccccn4)c3)c2)nc1

nearest known ligand 0.47

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 0.47
TLR2 O60603 1/20 0.47
ALOX15 P16050 1/20 0.42
ALDH1A1 P00352 2/20 0.42
KDM4E B2RXH2 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
GPR132 Q9UNW8 1/20 0.42
KMT2A Q03164 2/20 0.42
MEN1 O00255 1/20 0.42
ADAMTS4 O75173 1/20 0.41
PARP10 Q53GL7 1/20 0.40
KCNH2 Q12809 1/20 0.40
HDAC3 O15379 1/20 0.39
HDAC4 P56524 1/20 0.39
HDAC1 Q13547 1/20 0.39
HDAC7 Q8WUI4 1/20 0.39
HDAC2 Q92769 1/20 0.39
HDAC10 Q969S8 1/20 0.39
HDAC11 Q96DB2 1/20 0.39
HDAC8 Q9BY41 1/20 0.39

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
SCHEMBL6140596 0.92 TLR4 (0.45) TLR4TLR2ALDH1A1KDM4ESMN1; SMN2
SCHEMBL6140242 0.90 TLR4 (0.43) TLR4TLR2ALOX15ALDH1A1KDM4E
SCHEMBL6140428 0.89 TLR4 (0.39) TLR4TLR2ALOX15ALDH1A1KDM4E
SCHEMBL6140465 0.84 ALDH1A1 (0.45) TLR4TLR2ALDH1A1KDM4ESMN1; SMN2
SCHEMBL6140200 0.83 POLB (0.42) TLR4TLR2ALDH1A1KDM4ESMN1; SMN2
SCHEMBL6140710 0.83 TLR4 (0.46) TLR4TLR2SMN1; SMN2GPR132KMT2A
SCHEMBL6140741 0.83 SMN1; SMN2 (0.39) TLR4TLR2ALDH1A1KDM4ESMN1; SMN2
SCHEMBL6140822 0.83 SMN1; SMN2 (0.39) TLR4TLR2ALDH1A1KDM4ESMN1; SMN2
SCHEMBL6140135 0.82 TLR4 (0.41) TLR4TLR2ALDH1A1KDM4ESMN1; SMN2
SCHEMBL6140203 0.79 TLR4 (0.38) TLR4TLR2ALDH1A1SMN1; SMN2ADAMTS4

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