Potassium Ion

Potassium Ion

SCHEMBL2077835

O=C1c2ccccc2C(=O)c2cc(S(=O)(=O)[O-])ccc21.O=S(=O)([O-])OOS(=O)(=O)[O-].[K+].[Na+].[Na+]

nearest known ligand 0.53

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AGTR1DHFRGABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTNR3C2PBP2XPTGS1PTGS2VKORC1blablaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAftsImrcAmrcBmrdApbp1apbp1bpbp2apbp2bpbp3polthyA

The experimentally established mechanism targets of Potassium Ion. 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
PKLR P30613 4/20 0.53
PARG Q86W56 7/20 0.50
SMN1; SMN2 Q16637 3/20 0.47
KMT2A Q03164 3/20 0.47
MAPK1 P28482 2/20 0.47
MEN1 O00255 2/20 0.47
MAPT P10636 2/20 0.47
PKM P14618 1/20 0.47
HTT P42858 1/20 0.47
FTO Q9C0B1 1/20 0.43
STAT3 P40763 1/20 0.43
PTPN1 P18031 2/20 0.42
PGAM1 P18669 1/20 0.42
ELANE P08246 1/20 0.42
NPC1 O15118 1/20 0.42
ALDH1A1 P00352 1/20 0.42
TP53 P04637 1/20 0.42
CYP3A4 P08684 1/20 0.42
TSHR P16473 1/20 0.42
RAB9A P51151 1/20 0.42

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
Potassium Ion SCHEMBL10938667 1.00 PKLR (0.53) PKLRPARGSMN1; SMN2KMT2AMAPK1
Ammonia Solution, Strong SCHEMBL6752114 0.90 PKLR (0.50) PKLRPARGSMN1; SMN2KMT2AMAPK1
SCHEMBL305527 0.89 PKLR (0.62) PKLRPARGSMN1; SMN2KMT2AMAPK1
SCHEMBL28367628 0.89 PKLR (0.62) PKLRPARGSMN1; SMN2KMT2AMAPK1
SCHEMBL32662068 0.89 PKLR (0.62) PKLRPARGSMN1; SMN2KMT2AMAPK1
SCHEMBL29384291 0.89 PKLR (0.62) PKLRPARGSMN1; SMN2KMT2AMAPK1
Potassium Ion SCHEMBL2784885 0.89 PARG (0.59) PKLRPARGSMN1; SMN2KMT2AMAPK1
Water SCHEMBL1976332 0.88 PKLR (0.60) PKLRPARGSMN1; SMN2KMT2AMAPK1
Water SCHEMBL30203790 0.88 PKLR (0.60) PKLRPARGSMN1; SMN2KMT2AMAPK1
SCHEMBL2858677 0.86 PARG (0.59) PKLRPARGSMN1; SMN2KMT2AMAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7977431-B2 Dithiocarbamic esters LANXESS DEUTSCHLAND GMBH (DE) 2011-07-12 US disclosed
US-20110015360-A1 DITHIOCARBAMIC ESTERS LANXESS DEUTSCHLAND GMBH (DE) 2011-01-20 US disclosed
US-7825193-B2 Dithiocarbamic esters LANXESS DEUTSCHLAND GMBH (DE) 2010-11-02 US disclosed
US-20070078229-A1 suitable for regulating the molecular weight during the polymerization of chloroprene and/or 2,3-dichlorobutadiene; compound purity; no sacrifice of polymerization rate; efficient; industrial scale ARLANXEO DEUTSCHLAND GMBH (DE) 2007-04-05 US disclosed
US-7169937-B2 Dithiocarbamic esters BAYER AKTIENGESELLSCHAFT (DE) 2007-01-30 US disclosed
US-20040110964-A1 Dithiocarbamic esters ARLANXEO DEUTSCHLAND GMBH (DE) 2004-06-10 US disclosed
EP-0648788-B1 Method for producing a polychloroprene latex DENKI KAGAKU KOGYO KK (JP) 1998-05-20 EP disclosed
US-5681891-A COPOLYMERIZING CHLOROPRENE WITH AN ETHYLENICALLY UNSATURATED CARBOXYLIC ACID IN PRESENCE OF POLYVINYL ALCOHOL DENKI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1997-10-28 US disclosed
US-5661205-A COPOLYMERIZED WITH AN ETHYLENICALLY UNSATURATED CARBOXYLIC ACID IN THE PRESENCE OF POLYVINYL ALCOHOL AND A GLYCOL ETHER; ADHESIVES DENKI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1997-08-26 US disclosed
EP-0626398-B1 Polychloroprene latex and its composition DENKI KAGAKU KOGYO KK (JP) 1996-11-06 EP disclosed
EP-0648788-A1 Method for producing a polychloroprene latex DENKI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1995-04-19 EP disclosed
EP-0626398-A1 Polychloroprene latex and its composition DENKI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1994-11-30 EP disclosed
US-4839447-A SODIUM DITHIONITE FORMADINESULFINIC ACID AND POTASSIUM PEROXYD ISULFATE REDOX INITIATORS BAYER AKTIENGESELLSCHAFT (DE) 1989-06-13 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 (2 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-20070078229-A1 suitable for regulating the molecular weight during the polymerization of chloroprene and/or 2,3-dichlorobutadiene; compound purity; no sacrifice of polymerization rate; efficient; industrial scale DDT, DHPS, CBR3 PKLR 629/4885PARG 233/4885SMN1; SMN2 4415/4885
US-20040110964-A1 Dithiocarbamic esters DDT, DECR1, PCCA PKLR 1679/4885PARG 300/4885SMN1; SMN2 4623/4885

“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.