Potassium Ion

Potassium Ion

SCHEMBL6691575

O=S([O-])c1ccc(Br)cc1.[K+]

nearest known ligand 0.42

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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
CYP2A6 P11509 1/20 0.42
NMT1 P30419 1/20 0.38
CA2 P00918 5/20 0.37
CA1 P00915 3/20 0.37
PLCG1 P19174 1/20 0.36
CES2 O00748 1/20 0.35
CES1 P23141 1/20 0.35
ALDH1A1 P00352 4/20 0.33
ALOX15 P16050 2/20 0.33
MAPK1 P28482 2/20 0.33
CA12 O43570 1/20 0.33
CA9 Q16790 1/20 0.33
MMP1 P03956 1/20 0.33
MMP2 P08253 1/20 0.33
MMP9 P14780 1/20 0.33
MMP8 P22894 1/20 0.33
MMP13 P45452 1/20 0.33
TDP1 Q9NUW8 1/20 0.30
F2 P00734 1/20 0.30
PRSS1 P07477 1/20 0.30

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 SCHEMBL6691569 0.95 CYP2A6 (0.42) CYP2A6NMT1CA2CA1PLCG1
SCHEMBL3015881 0.95 CYP2A6 (0.42) CYP2A6NMT1CA2CA1PLCG1
Water SCHEMBL3165297 0.92 CYP2A6 (0.40) CYP2A6NMT1CA2CA1PLCG1
SCHEMBL11420734 0.88 CYP2A6 (0.36) CYP2A6NMT1CA2CA1PLCG1
SCHEMBL11423419 0.88 CYP2A6 (0.36) CYP2A6NMT1CA2CA1PLCG1
Potassium Ion SCHEMBL1024086 0.74 ALDH1A1 (0.48) CYP2A6CA2CA1CES2CES1
Potassium Ion SCHEMBL6695829 0.74 CA1 (0.37) CA2CA1MMP1MMP2MMP9
Potassium Ion SCHEMBL11323343 0.74 CA1 (0.37) CA2CA1CES2CES1ALDH1A1
Potassium Ion SCHEMBL6700152 0.74 LMNA (0.42) CYP2A6NMT1CA2CA1CES2
SCHEMBL5632523 0.73 CYP2A6 (0.45) CYP2A6NMT1ALDH1A1TDP1

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
US-20040034257-A1 Novel sulfone derivatives and process for producing these SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-02-19 US disclosed
EP-1359143-A1 NOVEL SULFONE DERIVATIVES AND PROCESS FOR PRODUCING THESE SUMITOMO CHEMICAL COMPANY LIMITED (JP) 2003-11-05 EP disclosed
US-4260552-A INSECTICIDES, HERBICIDES UNIROYAL, INC. (US) 1981-04-07 US disclosed
US-4160846-A Method for controlling insects with tetrasubstituted organotin compounds UNIROYAL, INC. (US) 1979-07-10 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-20040034257-A1 Novel sulfone derivatives and process for producing these RBP4, ADH4, RARB CYP2A6 103/4885NMT1 2950/4885CA2 3444/4885

“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.