Potassium Ion

Potassium Ion

SCHEMBL2784885

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

nearest known ligand 0.59

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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
PARG Q86W56 7/20 0.59
PKLR P30613 3/20 0.59
KMT2A Q03164 4/20 0.56
SMN1; SMN2 Q16637 3/20 0.56
MEN1 O00255 3/20 0.56
MAPK1 P28482 2/20 0.56
MAPT P10636 2/20 0.56
PKM P14618 1/20 0.56
HTT P42858 1/20 0.56
ELANE P08246 1/20 0.50
STAT3 P40763 1/20 0.50
CDC25B P30305 1/20 0.50
NPC1 O15118 1/20 0.50
ALDH1A1 P00352 1/20 0.50
TP53 P04637 1/20 0.50
CYP3A4 P08684 1/20 0.50
TSHR P16473 1/20 0.50
RAB9A P51151 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
BCL2 P10415 1/20 0.48

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
SCHEMBL8985955 0.96 PARG (0.59) PARGPKLRKMT2ASMN1; SMN2MEN1
SCHEMBL29384291 0.96 PKLR (0.62) PARGPKLRKMT2ASMN1; SMN2MEN1
Silver SCHEMBL11327330 0.96 PARG (0.59) PARGPKLRKMT2ASMN1; SMN2MEN1
SCHEMBL28367628 0.96 PKLR (0.62) PARGPKLRKMT2ASMN1; SMN2MEN1
SCHEMBL9235321 0.96 PARG (0.59) PARGPKLRKMT2ASMN1; SMN2MEN1
SCHEMBL32662068 0.96 PKLR (0.62) PARGPKLRKMT2ASMN1; SMN2MEN1
SCHEMBL2858677 0.96 PARG (0.59) PARGPKLRKMT2ASMN1; SMN2MEN1
SCHEMBL305527 0.96 PKLR (0.62) PARGPKLRKMT2ASMN1; SMN2MEN1
Water SCHEMBL30203790 0.94 PKLR (0.60) PARGPKLRKMT2ASMN1; SMN2MEN1
Water SCHEMBL1976332 0.94 PKLR (0.60) PARGPKLRKMT2ASMN1; SMN2MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107442167-B Catalyst for preparing aromatic polycarboxylic acid by liquid phase oxidation 中国石油化工股份有限公司 2020-05-05 CN disclosed
EP-2218715-B1 PHOTOACID GENERATOR AND PHOTOREACTIVE COMPOSITION SUMITOMO SEIKA CHEMICALS (JP) 2017-06-28 EP disclosed
US-8216768-B2 Photoacid generator and photoreactive composition SUMITOMO SEIKA CHEMICALS CO., LTD. (JP) 2012-07-10 US disclosed
US-20100233621-A1 PHOTOACID GENERATOR AND PHOTOREACTIVE COMPOSITION SUMITOMO SEIKA CHEMICALS CO., LTD. (JP) 2010-09-16 US disclosed
EP-2218715-A1 PHOTOACID GENERATOR AND PHOTOREACTIVE COMPOSITION Sumitomo Seika Chemicals CO. LTD. (JP) 2010-08-18 EP disclosed
US-3974170-A SULFONATES, SULFINATES MONSANTO COMPANY (US) 1976-08-10 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-20100233621-A1 PHOTOACID GENERATOR AND PHOTOREACTIVE COMPOSITION ARSA, SULT1A1, CYBA PARG 3130/4885PKLR 1773/4885KMT2A 1455/4885

“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.