SCHEMBL6140482

SCHEMBL6140482

CC(C)(C)OC(=O)COc1ccc([S+](c2ccc(OCc3ccncc3)cc2)c2ccc(OCc3ccncc3)cc2)cc1.Cc1ccc(S(=O)(=O)[O-])cc1

nearest known ligand 0.44

Known targets — ChEMBL curated mechanism

CHRM1CHRM2CHRM3CHRM4CHRM5SLC6A2dacAdacBdacCftsImrcAmrcBmrdA

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
TSHR P16473 1/20 0.44
LMNA P02545 3/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
ALDH1A1 P00352 1/20 0.44
GPR119 Q8TDV5 2/20 0.41
RORC P51449 1/20 0.40
ADAMTS4 O75173 1/20 0.40
MMP13 P45452 1/20 0.40
MAOB P27338 1/20 0.40
MAPK14 Q16539 1/20 0.39
HTT P42858 1/20 0.39
PSEN1 P49768 1/20 0.39
PSEN2 P49810 1/20 0.39
APH1B Q8WW43 1/20 0.39
NCSTN Q92542 1/20 0.39
APH1A Q96BI3 1/20 0.39
PSENEN Q9NZ42 1/20 0.39
L3MBTL1 Q9Y468 2/20 0.38
MEN1 O00255 1/20 0.38
GAA P10253 1/20 0.38

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
SCHEMBL6140591 1.00 TSHR (0.44) TSHRLMNASMN1; SMN2ALDH1A1GPR119
SCHEMBL6140463 0.93 F2 (0.41) TSHRLMNASMN1; SMN2ALDH1A1GPR119
SCHEMBL6140576 0.93 F2 (0.41) TSHRLMNASMN1; SMN2ALDH1A1GPR119
SCHEMBL6140690 0.92 PTPN1 (0.44) TSHRLMNASMN1; SMN2ALDH1A1GPR119
SCHEMBL6140091 0.92 PTPN1 (0.44) TSHRLMNASMN1; SMN2ALDH1A1GPR119
SCHEMBL6140500 0.90 RORC (0.41) TSHRLMNASMN1; SMN2ALDH1A1GPR119
SCHEMBL6140111 0.90 RORC (0.43) TSHRLMNASMN1; SMN2ALDH1A1GPR119
SCHEMBL8069405 0.89 PSEN1 (0.46) LMNASMN1; SMN2HTTPSEN1PSEN2
SCHEMBL8862147 0.89 PSEN1 (0.46) LMNASMN1; SMN2HTTPSEN1PSEN2
SCHEMBL8862192 0.89 PSEN1 (0.46) LMNASMN1; SMN2HTTPSEN1PSEN2

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