Potassium Ion

Potassium Ion

SCHEMBL3689408

Cc1sc2nc([S-])n(N)c(=O)c2c1C.[K+]

nearest known ligand 0.63

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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
GAK O14976 1/20 0.63
ALDH1A1 P00352 5/20 0.44
MAPK1 P28482 2/20 0.44
MAPT P10636 2/20 0.43
ATM Q13315 1/20 0.43
LMNA P02545 2/20 0.43
USP2 O75604 1/20 0.43
HTT P42858 1/20 0.43
HSD17B10 Q99714 3/20 0.42
KDM4E B2RXH2 2/20 0.42
NPC1 O15118 2/20 0.42
CASP1 P29466 2/20 0.42
CASP7 P55210 2/20 0.42
TP53 P04637 1/20 0.42
RXFP1 Q9HBX9 1/20 0.42
RAB9A P51151 2/20 0.42
HPGD P15428 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
NPSR1 Q6W5P4 1/20 0.42
TSHR P16473 1/20 0.41

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
SCHEMBL3754226 0.83 GAK (0.67) GAKALDH1A1MAPK1MAPTATM
SCHEMBL14360622 0.70 MAPT (0.54) GAKALDH1A1MAPK1MAPTATM
SCHEMBL7017261 0.68 MAPK1 (0.49) GAKALDH1A1MAPK1MAPTATM
Potassium Ion SCHEMBL3686147 0.68 MAPK1 (0.67) ALDH1A1MAPK1MAPTLMNAHTT
SCHEMBL1101894 0.66 MAPK1 (0.60) GAKALDH1A1MAPK1MAPTLMNA
SCHEMBL12877215 0.62 LMNA (0.79) ALDH1A1MAPK1MAPTLMNAUSP2
SCHEMBL16428676 0.62 MAPK1 (0.54) GAKALDH1A1MAPK1MAPTLMNA
SCHEMBL16298727 0.61 MAPK1 (1.00) ALDH1A1MAPK1MAPTLMNAKDM4E
SCHEMBL3754164 0.61 ALDH1A1 (0.56) ALDH1A1MAPK1MAPTATMLMNA
SCHEMBL13757221 0.60 MAPK1 (0.47) GAKALDH1A1MAPK1MAPTHSD17B10

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-1724267-B1 PYRIMIDINE DERIVATIVE ASKA PHARM CO LTD (JP) 2013-11-06 EP disclosed
US-7799775-B2 such as 3-amino-5,6-dimethyl-2-[3-(4-quinolin-2-ylpiperazin-1-yl)propylthio]-3H-thieno[2,3-d]pyrimidin-4-one, having serotonin receptor modulatory activity, used for treating irritable bowel syndrome ASKA PHARMACEUTICAL CO., LTD. (JP) 2010-09-21 US disclosed
US-20070197551-A1 Pyrimidine derivatives ASKA PHARMACEUTICAL CO., LTD. (JP) 2007-08-23 US disclosed
EP-1724267-A1 PYRIMIDINE DERIVATIVE ASKA Pharmaceutical Co., Ltd. (JP) 2006-11-22 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-20070197551-A1 Pyrimidine derivatives HTR3B, HTR3A, HTR1A GAK 2763/4885ALDH1A1 2838/4885MAPK1 2180/4885

“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.