Potassium Ion

Potassium Ion

SCHEMBL796078

O=C([O-])c1ccc(OC(F)(F)F)cn1.[K+]

nearest known ligand 0.45

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 17)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 2/20 0.45
MEN1 O00255 1/20 0.45
NPC1 O15118 3/20 0.43
RAB9A P51151 3/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
EPHX2 P34913 1/20 0.41
MAPK7 Q13164 1/20 0.40
TLR7 Q9NYK1 1/20 0.40
P4HTM Q9NXG6 2/20 0.39
SCN9A Q15858 2/20 0.38
SCN10A Q9Y5Y9 2/20 0.38
SCN7A Q01118 1/20 0.38
KCNH2 Q12809 1/20 0.38
HTT P42858 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
ABL1 P00519 4/20 0.38
CYP1A2 P05177 1/20 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
SCHEMBL29488317 0.83 P4HTM (0.53) KMT2AMEN1NPC1RAB9AL3MBTL1
SCHEMBL2300999 0.83 P4HTM (0.53) KMT2AMEN1NPC1RAB9AL3MBTL1
SCHEMBL30489408 0.81 KMT2A (0.57) KMT2AMEN1NPC1RAB9AL3MBTL1
SCHEMBL795658 0.81 MEN1 (0.49) KMT2AMEN1NPC1RAB9AL3MBTL1
SCHEMBL796465 0.80 MAPK1 (0.57) KMT2AMEN1NPC1RAB9AL3MBTL1
SCHEMBL18113755 0.78 MEN1 (0.46) KMT2AMEN1NPC1RAB9AL3MBTL1
SCHEMBL20271034 0.75 KMT2A (0.41) KMT2AMEN1NPC1RAB9AL3MBTL1
SCHEMBL18442520 0.75 KMT2A (0.41) KMT2AMEN1NPC1RAB9AL3MBTL1
SCHEMBL30342167 0.74 MEN1 (0.46) KMT2AMEN1NPC1RAB9AL3MBTL1
SCHEMBL16011698 0.74 P4HTM (0.58) L3MBTL1P4HTMCYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2616465-B1 TRIAZINE-OXADIAZOLES NOVARTIS AG (CH) 2015-11-04 EP disclosed
US-20150025057-A1 Triazine-oxadiazoles NOVARTIS AG (CH) 2015-01-22 US disclosed
US-8895733-B2 Triazine-oxadiazoles NOVARTIS AG (CH) 2014-11-25 US disclosed
US-20140051676-A1 Triazine-oxadiazoles NOVARTIS AG (CH) 2014-02-20 US disclosed
EP-2616465-A1 TRIAZINE-OXADIAZOLES Novartis AG (CH) 2013-07-24 EP disclosed
WO-2012035023-A1 TRIAZINE-OXADIAZOLES NOVARTIS AG (CH) 2012-03-22 WO 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 (2 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-20150025057-A1 Triazine-oxadiazoles OPRK1, OPRD1, OPRL1 KMT2A 3938/4885MEN1 4842/4885NPC1 3204/4885
US-20140051676-A1 Triazine-oxadiazoles OPRK1, OPRD1, OPRL1 KMT2A 3938/4885MEN1 4842/4885NPC1 3204/4885

“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.