Potassium Ion

Potassium Ion

SCHEMBL3700596

O=S(=O)([O-])c1c(Cl)ccc2c1ccc1c3ccccc3ccc21.[K+]

nearest known ligand 0.47

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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
HPRT1 P00492 5/20 0.47
CYP2A6 P11509 4/20 0.44
PAX8 Q06710 1/20 0.44
MAPT P10636 2/20 0.41
LMNA P02545 2/20 0.41
MAPK1 P28482 2/20 0.41
CYP3A4 P08684 1/20 0.41
APEX1 P27695 1/20 0.41
PMP22 Q01453 1/20 0.41
ALDH1A1 P00352 3/20 0.40
TDP1 Q9NUW8 2/20 0.40
HSD17B10 Q99714 2/20 0.40
TSHR P16473 1/20 0.40
CYP1A2 P05177 4/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
HIF1A Q16665 2/20 0.36
CYP2C9 P11712 2/20 0.36
CYP2C19 P33261 2/20 0.36
MEN1 O00255 1/20 0.36
USP2 O75604 1/20 0.36

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 SCHEMBL3804086 1.00 HPRT1 (0.47) HPRT1CYP2A6PAX8MAPTLMNA
Lithium Ion SCHEMBL3703515 0.97 HPRT1 (0.47) HPRT1CYP2A6PAX8MAPTLMNA
SCHEMBL3800115 0.97 HPRT1 (0.47) HPRT1CYP2A6PAX8MAPTLMNA
SCHEMBL3695173 0.97 HPRT1 (0.47) HPRT1CYP2A6PAX8MAPTLMNA
Lithium Ion SCHEMBL3808003 0.97 HPRT1 (0.47) HPRT1CYP2A6PAX8MAPTLMNA
Potassium Ion SCHEMBL3713251 0.91 CYP2A6 (0.48) HPRT1CYP2A6PAX8MAPTALDH1A1
Lithium Ion SCHEMBL3702126 0.88 CYP2A6 (0.48) HPRT1CYP2A6PAX8MAPTALDH1A1
Silver SCHEMBL11723519 0.88 CYP2A6 (0.48) HPRT1CYP2A6PAX8MAPTALDH1A1
SCHEMBL3696173 0.88 CYP2A6 (0.48) HPRT1CYP2A6PAX8MAPTALDH1A1
SCHEMBL3707634 0.81 HPRT1 (0.48) HPRT1CYP2A6PAX8MAPTLMNA

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
EP-2460789-B1 METHOD FOR PRODUCING BIARYL COMPOUND SUMITOMO CHEMICAL CO (JP) 2017-04-19 EP disclosed
US-9079830-B2 Method for producing biaryl compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-07-14 US disclosed
EP-2460789-A1 METHOD FOR PRODUCING BIARYL COMPOUND Sumitomo Chemical Company, Limited (JP) 2012-06-06 EP disclosed
US-20120123154-A1 METHOD FOR PRODUCING BIARYL COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-05-17 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-20120123154-A1 METHOD FOR PRODUCING BIARYL COMPOUND AKR7A2, AOC2, CBR1 HPRT1 1619/4885CYP2A6 47/4885PAX8 4776/4885

“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.