Potassium Ion

Potassium Ion

SCHEMBL17201768

O=C([O-])c1cccnc1-c1cccc(-c2ccc(Cl)cc2)n1.[K+]

nearest known ligand 0.43

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
KMO O15229 1/20 0.43
PARP1 P09874 1/20 0.41
MAP4K4 O95819 1/20 0.40
RORB Q92753 1/20 0.40
SMO Q99835 1/20 0.40
CTRC Q99895 1/20 0.39
CSNK2A2 P19784 1/20 0.39
CSNK2B P67870 1/20 0.39
PPARG P37231 1/20 0.39
TDP1 Q9NUW8 2/20 0.38
RAB9A P51151 2/20 0.38
KDM4E B2RXH2 2/20 0.38
ALDH1A1 P00352 1/20 0.38
GLA P06280 1/20 0.38
GAA P10253 1/20 0.38
HPGD P15428 1/20 0.38
EGFR P00533 1/20 0.38
MEN1 O00255 2/20 0.38
KMT2A Q03164 2/20 0.38
CNR2 P34972 1/20 0.38

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
SCHEMBL15567980 0.86 KDM4E (0.54) KMOPARP1MAP4K4RORBSMO
SCHEMBL17201767 0.85 KDM4E (0.53) KMOPARP1MAP4K4RORBSMO
Potassium SCHEMBL17201770 0.85 KDM4E (0.53) KMOPARP1MAP4K4RORBSMO
SCHEMBL15569111 0.82 NPC1 (0.55) KMOPARP1SMOTDP1RAB9A
SCHEMBL15567982 0.75 KMO (0.45) KMOMAP4K4SMOCTRCRAB9A
SCHEMBL15467862 0.75 KDM4E (0.61) PARP1SMOTDP1RAB9AKDM4E
Potassium Ion SCHEMBL29077360 0.74 P4HTM (0.51) TDP1RAB9AKDM4EALDH1A1HPGD
SCHEMBL17201766 0.73 KDM4E (0.58) KMOMAP4K4CTRCCSNK2A2CSNK2B
SCHEMBL7040626 0.72 P4HTM (0.49) TDP1RAB9AKDM4EALDH1A1HPGD
SCHEMBL31558943 0.72 P4HTM (0.49) TDP1RAB9AKDM4EALDH1A1HPGD

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-9409881-B2 Herbicidally active 6′-phenyl-2,2′-bipyridine-3-carboxylic acid derivatives BAYER CROPSCIENCE AG (AG) 2016-08-09 US disclosed
US-20150307470-A1 HERBICIDALLY ACTIVE 6'-PHENYL-2,2'-BIPYRIDINE-3-CARBOXYLIC ACID DERIVATIVES BAYER CROPSCIENCE AG (DE) 2015-10-29 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-20150307470-A1 HERBICIDALLY ACTIVE 6'-PHENYL-2,2'-BIPYRIDINE-3-CARBOXYLIC ACID DERIVATIVES CBR3, DDT, CBR1 KMO 574/4885PARP1 1868/4885MAP4K4 2905/4885

“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.