Potassium Ion

Potassium Ion

SCHEMBL561597

O=C([O-])CCON(Cc1ccccc1)Cc1ccccc1.[K+]

nearest known ligand 0.46

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
HDAC3 O15379 1/20 0.46
HDAC4 P56524 1/20 0.46
HDAC1 Q13547 1/20 0.46
HDAC7 Q8WUI4 1/20 0.46
HDAC2 Q92769 1/20 0.46
HDAC10 Q969S8 1/20 0.46
HDAC11 Q96DB2 1/20 0.46
HDAC8 Q9BY41 1/20 0.46
HDAC6 Q9UBN7 1/20 0.46
HDAC9 Q9UKV0 1/20 0.46
HDAC5 Q9UQL6 1/20 0.46
NPC1 O15118 3/20 0.42
RAB9A P51151 2/20 0.42
TDP1 Q9NUW8 1/20 0.40
KMT2A Q03164 3/20 0.39
CA12 O43570 1/20 0.39
CA9 Q16790 1/20 0.39
LMNA P02545 2/20 0.38
ALOX15 P16050 1/20 0.38
TSHR P16473 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
SCHEMBL7920783 0.84 KEAP1 (0.48) HDAC3HDAC4HDAC1HDAC7HDAC2
SCHEMBL561596 0.83 KEAP1 (0.47) HDAC3HDAC4HDAC1HDAC7HDAC2
SCHEMBL562070 0.79 KDM4E (0.49) NPC1RAB9ATDP1KMT2ACA12
SCHEMBL2238587 0.76 ALOX5 (0.49) NPC1RAB9ATDP1KMT2ALMNA
SCHEMBL2241139 0.76 TDP1 (0.51) NPC1RAB9ATDP1LMNAALOX15
SCHEMBL10352510 0.75 TDP1 (0.46) NPC1RAB9ATDP1KMT2ACA12
SCHEMBL9856644 0.74 NPC1 (0.43) HDAC3HDAC1HDAC2HDAC6NPC1
SCHEMBL9856413 0.73 BCHE (0.60) NPC1RAB9AKMT2ASMN1; SMN2
SCHEMBL10777388 0.72 ALDH1A1 (0.43) HDAC3HDAC4HDAC1HDAC7HDAC2
SCHEMBL10495848 0.71 ALDH1A1 (0.46) KMT2ATSHRMEN1SMN1; SMN2ALDH1A1

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 133 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2880092-B1 PHOSPHITE COMPOSITIONS SI GROUP SWITZERLAND CHAA GMBH (CH) 2020-09-30 EP disclosed
EP-2459576-B1 LIQUID ALKYLATED TRISARYL PHOSPHITE COMPOSITIONS HAVING TWO ALKYL GROUPS WITH DIFFERENT CARBON NUMBER ADDIVANT SWITZERLAND GMBH (CH) 2018-11-21 EP disclosed
EP-2459575-B2 HYDROLYTICALLY STABLE PHOSPHITE COMPOSITIONS ADDIVANT SWITZERLAND GMBH (CH) 2018-07-25 EP disclosed
EP-2917276-B1 STABILIZED HIGH-DENSITY POLYETHYLENE COMPOSITION WITH IMPROVED RESISTANCE TO DETERIORATION AND STABILZER SYSTEM EQUISTAR CHEM LP (US) 2018-07-18 EP disclosed
EP-2459574-B1 SOLID ALKYLARYL PHOSPHITE COMPOSITIONS AND METHODS FOR MANUFACTURING SAME ADDIVANT SWITZERLAND GMBH (CH) 2018-06-20 EP disclosed
EP-2491078-B1 POLYMERS WITH LOW GEL CONTENT AND ENHANCED GAS-FADING ADDIVANT SWITZERLAND GMBH (CH) 2016-09-28 EP disclosed
EP-2917276-A1 STABILIZED HIGH-DENSITY POLYETHYLENE COMPOSITION WITH IMPROVED RESISTANCE TO DETERIORATION AND STABILZER SYSTEM Equistar Chemicals LP (US) 2015-09-16 EP disclosed
EP-2459578-B1 SOLID ALKYLARYL PHOSPHITE COMPOSITIONS AND METHODS FOR MANUFACTURING SAME ADDIVANT SWITZERLAND GMBH (CH) 2015-08-19 EP disclosed
EP-2880092-A1 PHOSPHITE COMPOSITIONS Addivant Switzerland GmbH (CH) 2015-06-10 EP disclosed
US-20150073073-A1 PHOSPHITE COMPOSITIONS ADDIVANT USA, LLC 2015-03-12 US disclosed
US-5141975-A Melt processability, discoloration inhibition GENERAL ELECTRIC COMPANY (US) 1992-08-25 US disclosed
US-5142083-A Melt flow and color stabilization of thermoplastics GENERAL ELECTRIC COMPANY (US) 1992-08-25 US disclosed
US-5137950-A Reacting phosphorous trichloride with alcohol; polymer stabilizer BORG-WARNER SPECIALTY CHEMICALS, INC. (US) 1992-08-11 US disclosed
US-5124472-A From tetrahydroabiethyl alcohol GENERAL ELECTRIC COMPANY (US) 1992-06-23 US disclosed
EP-0460461-A1 Hydrolytically stable phosphites GENERAL ELECTRIC COMPANY (US) 1991-12-11 EP disclosed
US-5023285-A Melt flow and color stabilizers for polymers G E SPECIALTY CHEMICALS (US) 1991-06-11 US disclosed
EP-0240462-B1 SUBSTITUTED AMINOOXYPROPANOATE CIBA-GEIGY AG (CH) 1990-08-01 EP disclosed
EP-0356687-A1 Bis (tri-tertiary-alkylphenoxy) diphosphaspiroundecanes GE SPECIALTY CHEMICALS, INC. (US) 1990-03-07 EP disclosed
EP-0356688-A2 3, 9-diphosphaspiroundecanes and process for making 3, 9-diphosphaspiroundecanes GE SPECIALTY CHEMICALS, INC. (US) 1990-03-07 EP disclosed
EP-0240462-A2 Substituted aminooxypropanoate CIBA-GEIGY AG (CH) 1987-10-07 EP disclosed