SCHEMBL751070

SCHEMBL751070

O=S(=O)([O-])CCSCCS(=O)(=O)[O-].[Na+].[Na+]

nearest known ligand 0.48

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 17)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 1/20 0.48
MAPT P10636 1/20 0.48
ALOX15 P16050 1/20 0.48
ALDH1A1 P00352 2/20 0.43
TSHR P16473 2/20 0.43
GMNN O75496 1/20 0.43
LMNA P02545 1/20 0.43
TP53 P04637 1/20 0.43
MAPK1 P28482 1/20 0.43
THPO P40225 1/20 0.43
HBB P68871 1/20 0.43
PMP22 Q01453 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
BBOX1 O75936 3/20 0.36
ENPEP Q07075 2/20 0.36
MEN1 O00255 1/20 0.32
KMT2A Q03164 1/20 0.32

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
Lithium Ion SCHEMBL3277139 0.94 KDM4E (0.41) KDM4EMAPTALOX15ALDH1A1TSHR
SCHEMBL29283219 0.87 KDM4E (0.56) KDM4EMAPTALOX15ALDH1A1TSHR
SCHEMBL8459071 0.84 BBOX1 (0.40) KDM4EMAPTALOX15ALDH1A1TSHR
SCHEMBL29283223 0.83 KDM4E (0.52) KDM4EMAPTALOX15ALDH1A1TSHR
SCHEMBL28899359 0.82 GMNN (0.52) KDM4EMAPTALOX15ALDH1A1TSHR
2,2'-Dithiodiethanesulfonic Acid SCHEMBL18847 0.81 KDM4E (0.48) KDM4EMAPTALOX15ALDH1A1TSHR
2,2'-Dithiodiethanesulfonic Acid SCHEMBL835029 0.81 KDM4E (0.48) KDM4EMAPTALOX15ALDH1A1TSHR
SCHEMBL27175717 0.80 GMNN (0.50) KDM4EMAPTALOX15ALDH1A1TSHR
SCHEMBL3890653 0.80 GMNN (0.50) KDM4EMAPTALOX15ALDH1A1TSHR
2,2'-Dithiodiethanesulfonic Acid SCHEMBL835873 0.79 KDM4E (0.46) KDM4EMAPTALOX15ALDH1A1TSHR

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-8449957-B2 Recording medium CANON KABUSHIKI KAISHA (JP) 2013-05-28 US disclosed
US-20120070591-A1 RECORDING MEDIUM CANON KABUSHIKI KAISHA (JP) 2012-03-22 US disclosed
EP-2431189-A2 Recording medium Canon Kabushiki Kaisha (JP) 2012-03-21 EP disclosed
EP-1694637-A4 PROCESS FOR SYNTHESIZING DISULFIDES BIONUMERIK PHARMACEUTICALS INC (US) 2007-09-26 EP disclosed
EP-1694637-A2 PROCESS FOR SYNTHESIZING DISULFIDES BIONUMERIK PHARMACEUTICALS, INC. (US) 2006-08-30 EP disclosed
US-7053240-B2 Process for synthesizing disulfides BIONUMERIK PHARMACEUTICALS, INC. (US) 2006-05-30 US disclosed
WO-2005058005-A2 PROCESS FOR SYNTHESIZING DISULFIDES BIONUMERIK PHARMACEUTICALS, INC. (US) 2005-06-30 WO disclosed
US-20050137419-A1 Process for synthesizing disulfides BIONUMERIK PHARMACEUTICALS, INC. 2005-06-23 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-20050137419-A1 Process for synthesizing disulfides TST, CBS, STS KDM4E 3498/4885MAPT 3687/4885ALOX15 2286/4885

“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.