SCHEMBL7159703

SCHEMBL7159703

O=S(=O)([O-])Oc1ccc(O)c2ccccc12.[Na+]

nearest known ligand 0.50

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
ESR2 known ✓ Q92731 3/20 0.50
THRB known ✓ P10828 1/20 0.40
GAA P10253 5/20 0.50
MEN1 O00255 4/20 0.50
KMT2A Q03164 4/20 0.50
ESR1 P03372 3/20 0.50
IDO1 P14902 4/20 0.48
LDHA P00338 1/20 0.47
EP300 Q09472 3/20 0.42
KAT2B Q92831 3/20 0.42
KAT8 Q9H7Z6 3/20 0.42
CTSB P07858 1/20 0.42
MAPT P10636 3/20 0.40
ALOX15 P16050 3/20 0.40
SMN1; SMN2 Q16637 3/20 0.40
HSD17B10 Q99714 3/20 0.40
HKDC1 Q2TB90 2/20 0.40
ALDH1A1 P00352 2/20 0.40
TP53 P04637 2/20 0.40
HPGD P15428 2/20 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
SCHEMBL7156677 0.89 ESR1 (0.62) GAAMEN1KMT2AESR1ESR2
SCHEMBL974174 0.88 F11 (0.40) GAAMEN1KMT2AESR1ESR2
SCHEMBL627133 0.83 GAA (0.50) GAAMEN1KMT2AESR1ESR2
SCHEMBL974086 0.80 GAA (0.46) GAAMEN1KMT2AESR1ESR2
SCHEMBL1937408 0.79 HSD11B1 (0.51) GAAMEN1KMT2AESR1ESR2
Hydrogen Sulfide SCHEMBL27642870 0.76 KMT2A (0.81) GAAMEN1KMT2AESR1ESR2
SCHEMBL4094195 0.75 ELANE (0.40) SMN1; SMN2ALDH1A1LMNAHTT
Potassium Ion SCHEMBL11017575 0.74 PTPN22 (0.44) MEN1KMT2ALDHAMAPT
SCHEMBL8321795 0.74 CTSB (0.39) GAAMEN1KMT2AESR1ESR2
SCHEMBL18316005 0.74 COMT (0.55) MEN1KMT2AIDO1CTSBMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8637221-B2 Lithographic printing plate precursor, plate making method thereof and novel polymer compound FUJIFILM CORPORATION (JP) 2014-01-28 US disclosed
US-20130089818-A1 LITHOGRAPHIC PRINTING PLATE PRECURSOR, PLATE MAKING METHOD THEREOF AND NOVEL POLYMER COMPOUND FUJIFILM CORPORATION (JP) 2013-04-11 US disclosed
US-6541178-B2 An sulfonium(-) and iodonium(+)ion-type photoacid generator containing a naphthol structure, and photosensitive polyimide resin using photoacid generator SAMSUNG ELECTRONICS CO., LTD. (KR) 2003-04-01 US disclosed
US-20020048719-A1 Ion-type photoacid generator containing naphthol and photosensitive polyimide composition prepared by using the same SAMSUNG ELECTRONICS CO., LTD. 2002-04-25 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20020048719-A1 Ion-type photoacid generator containing naphthol and photosensitive polyimide composition prepared by using the same ASIC1, H1-0, RER1 ESR2 698/4885THRB 3875/4885GAA 1509/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.