SCHEMBL6550358

SCHEMBL6550358

CCCCC(S)(CCCC)C(=O)C1CCCC1.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.41

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
ALDH1A1 P00352 8/20 0.41
LMNA P02545 3/20 0.39
RAB9A P51151 2/20 0.38
CYP2D6 P10635 2/20 0.38
MEN1 O00255 1/20 0.38
KMT2A Q03164 1/20 0.38
TSHR P16473 4/20 0.37
GAA P10253 2/20 0.37
RECQL P46063 2/20 0.37
POLB P06746 1/20 0.37
NPSR1 Q6W5P4 1/20 0.37
NPC1 O15118 1/20 0.37
ENPP3 O14638 2/20 0.37
ENPP1 P22413 2/20 0.37
ENPP2 Q13822 2/20 0.37
EPHX2 P34913 1/20 0.37
ALB P02768 1/20 0.36
CYP2C9 P11712 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
CYP3A4 P08684 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
SCHEMBL6551032 0.99 ALDH1A1 (0.43) ALDH1A1LMNARAB9ACYP2D6MEN1
SCHEMBL6549474 0.79 ALDH1A1 (0.40) ALDH1A1LMNARAB9AMEN1KMT2A
Trifluoromethanesulfonic Acid SCHEMBL6549572 0.78 NAAA (0.37) EPHX2
SCHEMBL6549858 0.78 NAAA (0.37) EPHX2
SCHEMBL6551025 0.77 NAAA (0.39) KMT2ATSHRGAAENPP3ENPP1
Trifluoromethanesulfonic Acid SCHEMBL6549822 0.77 NAAA (0.39) GAAEPHX2
Butylcyclohexane SCHEMBL31082847 0.76 CYP1A2 (0.51) ALDH1A1LMNARAB9ACYP2D6MEN1
Pentane SCHEMBL28482247 0.72 ALDH1A1 (0.50) ALDH1A1LMNACYP2D6MEN1KMT2A
Hexane SCHEMBL7122950 0.72 MCHR1 (0.53) ALDH1A1LMNAMEN1KMT2ATSHR
SCHEMBL6549325 0.72 NAAA (0.33)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1167349-B1 Chemical amplifying type positive resist composition SUMITOMO CHEMICAL CO (JP) 2004-12-01 EP disclosed
US-20020015913-A1 Chemical amplifying type positive resist composition and sulfonium salt SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-02-07 US disclosed
EP-1167349-A1 Chemical amplifying type positive resist composition and sulfonium salt SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-01-02 EP disclosed