Potassium Ion

Potassium Ion

SCHEMBL967647

CCCCCS(=O)(=O)[N-]C(=O)/C=C/c1c(C)nn(C)c1-c1cccc2ccccc12.[K+]

nearest known ligand 0.35

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
CNR2 P34972 11/20 0.35
NPC1 O15118 1/20 0.34
ALDH1A1 P00352 1/20 0.34
RAB9A P51151 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
TLR8 Q9NR97 1/20 0.34
CNR1 P21554 6/20 0.33
SLC6A3 Q01959 1/20 0.33
HTR2C P28335 1/20 0.32
EEF2K O00418 1/20 0.31
MARK3 P27448 1/20 0.31
AXL P30530 1/20 0.31
BCL6 P41182 1/20 0.31
NEK4 P51957 1/20 0.31
PRKCD Q05655 1/20 0.31
MCL1 Q07820 1/20 0.31
PRKAA1 Q13131 1/20 0.31
CAMK2B Q13554 1/20 0.31
CAMK2G Q13555 1/20 0.31
CAMK2D Q13557 1/20 0.31

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
SCHEMBL964737 0.83 PPARG (0.40) CNR2NPC1ALDH1A1RAB9ASMN1; SMN2
SCHEMBL964739 0.83 PPARG (0.40) CNR2NPC1ALDH1A1RAB9ASMN1; SMN2
Potassium Ion SCHEMBL962884 0.79 ALDH1A1 (0.34) CNR2NPC1ALDH1A1RAB9ASMN1; SMN2
SCHEMBL963941 0.77 ALDH1A1 (0.51) NPC1ALDH1A1RAB9ASMN1; SMN2HTR2C
SCHEMBL963943 0.77 ALDH1A1 (0.51) NPC1ALDH1A1RAB9ASMN1; SMN2HTR2C
Potassium Ion SCHEMBL962180 0.77 ASAH1 (0.35) NPC1ALDH1A1RAB9ASMN1; SMN2
Potassium Ion SCHEMBL963263 0.75 NPC1 (0.31) NPC1ALDH1A1RAB9ASMN1; SMN2
Potassium Ion SCHEMBL966881 0.74 HDAC3 (0.32) CNR2NPC1ALDH1A1RAB9ASMN1; SMN2
Potassium Ion SCHEMBL963147 0.74 NOTUM (0.33) CNR2NPC1ALDH1A1RAB9ASMN1; SMN2
Potassium Ion SCHEMBL962489 0.71

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110009384-A1 FUSED RING COMPOUNDS AS PARTIAL AGONISTS OF PPAR-GAMMA TAKEDA PHARMACEUTICAL COMPANY LIMITED 2011-01-13 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-20110009384-A1 FUSED RING COMPOUNDS AS PARTIAL AGONISTS OF PPAR-GAMMA PPARA, PPARD, PPARG CNR2 290/4885NPC1 1538/4885ALDH1A1 821/4885

“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.