Potassium Ion

Potassium Ion

SCHEMBL830772

Cc1ccc(-c2cc(CC(C)C)c(C(=O)[O-])c(C(F)(F)F)n2)cc1.[K+]

nearest known ligand 0.37

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 18)

geneUniProtsupporting neighboursconfidence
PTGS2 known ✓ P35354 1/20 0.34
PTGS1 known ✓ P23219 1/20 0.34
DPP4 P27487 3/20 0.37
DPP8 Q6V1X1 3/20 0.37
KDM4E B2RXH2 1/20 0.37
SDHB P21912 1/20 0.37
DPP9 Q86TI2 2/20 0.36
MAPT P10636 2/20 0.36
POLB P06746 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
ADORA3 P0DMS8 4/20 0.36
PTGER1 P34995 2/20 0.35
PTGER3 P43115 1/20 0.35
DHODH Q02127 2/20 0.35
ALDH1A1 P00352 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
ADORA1 P30542 2/20 0.34
RAD51 Q06609 1/20 0.34

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
Potassium Ion SCHEMBL829507 0.91 PTGER1 (0.41) ADORA3PTGER1PTGER3DHODHALDH1A1
SCHEMBL839634 0.88 DPP4 (0.46) DPP4DPP8KDM4ESDHBDPP9
Potassium Ion SCHEMBL830613 0.88 SDHB (0.40) DPP4SDHBDHODHALDH1A1
SCHEMBL830771 0.87 DPP4 (0.45) DPP4DPP8KDM4ESDHBDPP9
SCHEMBL831044 0.84 ALDH1A1 (0.50) DPP4KDM4EMAPTPOLBSMN1; SMN2
SCHEMBL839635 0.79 DHODH (0.42) MAPTPOLBADORA3DHODH
SCHEMBL829506 0.78 DHODH (0.41) MAPTPOLBADORA3DHODH
SCHEMBL831460 0.77 ALDH1A1 (0.49) KDM4EMAPTPOLBSMN1; SMN2ADORA3
SCHEMBL839855 0.76 GFER (0.42) DPP4DPP8SDHBMAPTDHODH
Potassium SCHEMBL830614 0.76 GFER (0.41) DPP4DPP8SDHBMAPTDHODH

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-8143411-B2 Substituted 6-phenylnicotinic acids and their use BAYER ANIMAL HEALTH GMBH (DE) 2012-03-27 US disclosed
US-20100234432-A1 Substituted 6-phenylnicotinic acids and their use BAYER ANIMAL HEALTH GMBH (DE) 2010-09-16 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-20100234432-A1 Substituted 6-phenylnicotinic acids and their use SLC5A6, FABP3, NAPRT PTGS2 2616/4885PTGS1 2015/4885DPP4 466/4885

“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.