Potassium Ion

Potassium Ion

SCHEMBL7511076

O=[N+]([O-])c1cccc(S(=O)[O-])c1.[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 19)

geneUniProtsupporting neighboursconfidence
TSHR P16473 6/20 0.59
LMNA P02545 2/20 0.59
ALDH1A1 P00352 6/20 0.55
ALOX15 P16050 1/20 0.55
ACHE P22303 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
HSP90AA1 P07900 1/20 0.48
KMT2A Q03164 2/20 0.47
GAA P10253 1/20 0.47
HTT P42858 1/20 0.47
CES2 O00748 1/20 0.47
CES1 P23141 1/20 0.47
TP53 P04637 1/20 0.46
NFE2L2 Q16236 1/20 0.44
CA2 P00918 1/20 0.44
CA5A P35218 1/20 0.44
MEN1 O00255 1/20 0.44
FBP1 P09467 1/20 0.43
VCP P55072 1/20 0.43

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
SCHEMBL1584154 0.96 TSHR (0.59) TSHRLMNAALDH1A1ALOX15ACHE
SCHEMBL8440395 0.81 TSHR (0.59) TSHRLMNAALDH1A1ALOX15ACHE
SCHEMBL1584157 0.79 TSHR (0.57) TSHRLMNAALDH1A1ALOX15ACHE
SCHEMBL7511081 0.79 TSHR (0.57) TSHRLMNAALDH1A1ALOX15ACHE
Dinitrophenylene SCHEMBL28795037 0.77 TSHR (0.90) TSHRLMNAALDH1A1ALOX15ACHE
SCHEMBL17649054 0.77 TSHR (0.53) TSHRLMNAALDH1A1ALOX15ACHE
Dinitrophenylene SCHEMBL29291896 0.76 TSHR (1.00) TSHRLMNAALDH1A1ALOX15ACHE
Dinitrophenylene SCHEMBL36632 0.76 TSHR (1.00) TSHRLMNAALDH1A1ALOX15ACHE
Potassium Ion SCHEMBL6693540 0.75 ALDH1A1 (0.48) TSHRLMNAALDH1A1ACHETDP1
Dinitrophenylene SCHEMBL28073578 0.75 TSHR (0.77) TSHRLMNAALDH1A1ALOX15ACHE

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-1231197-A1 Process for producing allyl halide compound SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-08-14 EP disclosed
US-20020107422-A1 Process for producing allyl halide compound SUMITOMO CHEMICAL COMPANY LIMITED (JP) 2002-08-08 US 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-20020107422-A1 Process for producing allyl halide compound ENY2, ZYX, RPS4Y1 TSHR 3103/4885LMNA 2456/4885ALDH1A1 1133/4885

“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.