Potassium Ion

Potassium Ion

SCHEMBL7513503

O=S([O-])c1ccccc1Cl.[K+]

nearest known ligand 0.41

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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 18)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.41
LMNA P02545 1/20 0.41
KMT2A Q03164 2/20 0.40
NMT1 P30419 1/20 0.35
CES2 O00748 1/20 0.34
CES1 P23141 1/20 0.34
G6PD P11413 1/20 0.34
ALDH1A1 P00352 3/20 0.33
POLB P06746 1/20 0.31
CYP2A6 P11509 4/20 0.31
CYP1A2 P05177 3/20 0.31
MEN1 O00255 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
ERCC5 P28715 1/20 0.31
FEN1 P39748 1/20 0.31
MGLL Q99685 1/20 0.30
CYP11B1 P15538 1/20 0.30
CYP11B2 P19099 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
SCHEMBL29828186 0.95 TSHR (0.41) TSHRLMNAKMT2ANMT1CES2
Lithium Ion SCHEMBL7518786 0.95 TSHR (0.41) TSHRLMNAKMT2ANMT1CES2
SCHEMBL1465305 0.95 TSHR (0.41) TSHRLMNAKMT2ANMT1CES2
SCHEMBL1583998 0.77 TSHR (0.38) TSHRLMNAKMT2ANMT1ALDH1A1
SCHEMBL11859111 0.76 G6PD (0.42) G6PDALDH1A1TDP1
SCHEMBL345543 0.73 TSHR (0.43) TSHRLMNAKMT2ACES2CES1
Potassium Ion SCHEMBL11334527 0.73 TP53 (0.42) TSHRKMT2ANMT1ALDH1A1POLB
Potassium Ion SCHEMBL3152587 0.71 TSHR (0.41) TSHRG6PDALDH1A1CYP2A6CYP1A2
SCHEMBL7518790 0.71 TSHR (0.41) TSHRLMNAKMT2ACES2CES1
SCHEMBL1465308 0.71 TSHR (0.41) TSHRLMNAKMT2ACES2CES1

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 5 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
EP-0599199-B1 Silver halide photographic emulsions sensitized in the presence of organic disulfides and sulfinates EASTMAN KODAK CO (US) 1997-03-12 EP disclosed
US-5328820-A Precipitation of silver halide, sensitization and adding antifogging agents EASTMAN KODAK COMPANY (US) 1994-07-12 US disclosed
EP-0599199-A1 Silver halide photographic emulsions sensitized in the presence of organic disulfides and sulfinates EASTMAN KODAK COMPANY (US) 1994-06-01 EP 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 2456/4885KMT2A 1123/4885

“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.