Potassium Ion

Potassium Ion

SCHEMBL6851222

O=C([O-])c1c(-c2cc(C3CC3)cs2)c2ccccc2n1Cc1cccc(C(F)(F)F)c1.[K+]

nearest known ligand 0.44

Full drug profile on Sugi Atlas →

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
MAPT P10636 1/20 0.44
MAPK10 P53779 1/20 0.44
PPARG P37231 7/20 0.44
HDAC1 Q13547 1/20 0.40
HDAC8 Q9BY41 1/20 0.40
HDAC6 Q9UBN7 1/20 0.40
FABP4 P15090 2/20 0.39
CPT1A P50416 1/20 0.39
ALDH1A2 O94788 1/20 0.39
ALDH1A1 P00352 1/20 0.39
ALDH2 P05091 1/20 0.39
ALDH3A1 P30838 1/20 0.39
ALDH1A3 P47895 1/20 0.39
S1PR1 P21453 1/20 0.39
GRK5 P34947 1/20 0.39
CDK8 P49336 1/20 0.39
S1PR5 Q9H228 1/20 0.39
DRD4 P21917 1/20 0.38
CHRM4 P08173 1/20 0.38
SIGMAR1 Q99720 2/20 0.37

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
SCHEMBL7035429 0.91 MAPT (0.46) MAPTMAPK10PPARGFABP4CPT1A
SCHEMBL7110258 0.87 PPARG (0.45) MAPTMAPK10PPARGHDAC1HDAC8
Potassium Ion SCHEMBL6851213 0.77 PPARG (0.52) MAPTMAPK10PPARGHDAC1HDAC8
SCHEMBL24482671 0.74 MAPT (0.53) MAPTMAPK10PPARGHDAC1HDAC8
SCHEMBL6855595 0.70 MAPT (0.48) MAPTMAPK10PPARGFABP4
SCHEMBL24482780 0.69 CCR2 (0.65) MAPTMAPK10PPARGHDAC1HDAC8
SCHEMBL7039948 0.69 PPARG (0.59) MAPTMAPK10PPARGFABP4
SCHEMBL7035422 0.68 PPARG (0.53) MAPTMAPK10PPARGFABP4ALDH1A2
SCHEMBL6300362 0.68 MAPT (0.57) MAPTMAPK10PPARGHDAC1HDAC8
SCHEMBL27581403 0.67 PPARG (0.53) MAPTMAPK10PPARGFABP4ALDH1A2

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 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6787651-B2 2-CARBOXY-SUBSTITUTED; TREATING OSTEOPENIA, OSTEOPOROSIS, CANCER, DIABETES AND ATHEROSCLEROSIS. SMITHKLINE BEECHAM CORPORATION 2004-09-07 US disclosed
US-20030087902-A1 Substituted indoles, pharmaceutical compounds containing such indoles and their use as PPAR-gamma binding agents SMITHKLINE BEECHAM CORPORATION 2003-05-08 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-20030087902-A1 Substituted indoles, pharmaceutical compounds containing such indoles and their use as PPAR-gamma binding agents PPARG, PPARA, PPARD MAPT 3447/4885MAPK10 1496/4885PPARG 1/4885

“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.