Potassium Ion

Potassium Ion

SCHEMBL2787084

O=C1c2ccccc2C(=O)c2c1cccc2S(=O)(=O)[O-].[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
ALDH1A1 P00352 4/20 0.59
SMN1; SMN2 Q16637 2/20 0.59
PKLR P30613 5/20 0.56
PTPN1 P18031 3/20 0.56
PGAM1 P18669 2/20 0.56
ADORA2A P29274 1/20 0.50
FTO Q9C0B1 1/20 0.47
STAT3 P40763 1/20 0.47
MEN1 O00255 1/20 0.46
CDC25B P30305 1/20 0.46
KMT2A Q03164 1/20 0.46
L3MBTL1 Q9Y468 4/20 0.46
EGFR P00533 2/20 0.46
MAPT P10636 2/20 0.46
MAPK1 P28482 2/20 0.46
TDP1 Q9NUW8 2/20 0.46
LMNA P02545 2/20 0.46
PABPC1 P11940 1/20 0.46
RAB9A P51151 1/20 0.46
NSD2 O96028 1/20 0.46

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
SCHEMBL3511014 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PKLRPTPN1PGAM1
SCHEMBL31317955 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PKLRPTPN1PGAM1
SCHEMBL30469515 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PKLRPTPN1PGAM1
SCHEMBL1412691 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PKLRPTPN1PGAM1
SCHEMBL29622863 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PKLRPTPN1PGAM1
Silver SCHEMBL2958255 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PKLRPTPN1PGAM1
SCHEMBL5068680 0.96 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2PKLRPTPN1PGAM1
Water SCHEMBL28390010 0.94 ALDH1A1 (0.57) ALDH1A1SMN1; SMN2PKLRPTPN1PGAM1
Potassium Ion SCHEMBL2788338 0.94 STAT3 (0.52) ALDH1A1SMN1; SMN2PKLRPTPN1PGAM1
Potassium Ion SCHEMBL4797638 0.92 ALDH1A1 (0.49) ALDH1A1SMN1; SMN2PKLRPTPN1PGAM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4959753-A AN ELECTROLYTIC ELECTROCONDUCTIVE POLYMER DOPED WITH A NAPHTHALENE-OR ANTHRAQUINONESULFONATE ON A DIELECTRIC FILM FORMED FROM ANODIZING THE METAL SUBSTRATE; HEAT AND HUMIDITY RESISTANCE; SHELF LIFELEAK MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 1990-09-25 US claimed
EP-0358239-A2 Solid electrolytic capacitor and method of manufacturing the same MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 1990-03-14 EP claimed
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
WO-2002030906-A1 ANTI-TUMOUR COMPOUNDS LA TROBE UNIVERSITY (AU) 2002-04-18 WO disclosed
US-5912386-A Bridged anthraquinones BAYER AKTIENGESELLSCHAFT (DE) 1999-06-15 US disclosed
US-4021455-A Process for the manufacture of anthraquinonesulphonic acid BAYER AKTIENGESELLSCHAFT (DT) 1977-05-03 US disclosed
US-3971812-A Anthraquinone dyestuffs BAYER AKTIENGESELLSCHAFT (DT) 1976-07-27 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 ALDH1A1 261/4885SMN1; SMN2 4360/4885PKLR 1773/4885

“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.