Potassium Ion

Potassium Ion

SCHEMBL2955595

C[O-].[K+].[Na+].[OH-]

nearest known ligand 0.00

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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 SCHEMBL339434 0.91
Potassium Ion SCHEMBL14634347 0.91
Water SCHEMBL1014000 0.91
Potassium Ion SCHEMBL28108880 0.83
Water SCHEMBL28212090 0.83
Water SCHEMBL5129118 0.83
Potassium Ion SCHEMBL28320042 0.83
SCHEMBL2169602 0.82
Potassium Ion SCHEMBL6839 0.82
SCHEMBL81 0.82

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106916079-A A kind of synthetic method of the methacetin of the mark of carbon 13 中国农业科学院植物保护研究所 2017-07-04 CN claimed
US-20040225153-A1 Synthesis of polyphosphazenes with sulfonimide side groups THE PENN STATE RESEARCH FOUNDATION 2004-11-11 US claimed
WO-2004072141-A2 SYNTHESIS OF POLYPHOSPHAZENES WITH SULFONIMIDE SIDE GROUPS THE PENN STATE RESEARCH FOUNDATION (US) 2004-08-26 WO claimed
US-4372971-A Heterocyclic prostaglandin type compounds, medicaments containing them and processes for the preparation and use of these heterocyclic compounds and medicaments GRUENENTHAL GMBH (DE) 1983-02-08 US claimed
CN-118620007-A Chiral tetradentate phosphine ligand compound, and preparation method and application thereof 凯特立斯(深圳)科技有限公司 2024-09-10 CN disclosed
EP-3250546-A1 LATENT HEAT STORAGE USING RENEWABLE PHASE CHANGE MATERIALS Trent University (CA) 2017-12-06 EP disclosed
CN-107163092-A The preparation method of the diabetes inhibitor of SGLT 2 and its intermediate 杭州科巢生物科技有限公司 2017-09-15 CN disclosed
CN-106916079-A A kind of synthetic method of the methacetin of the mark of carbon 13 中国农业科学院植物保护研究所 2017-07-04 CN disclosed
US-9434674-B2 Latent heat storage using renewable phase change materials TRENT UNIVERSITY (CA) 2016-09-06 US disclosed
WO-2016120738-A1 LATENT HEAT STORAGE USING RENEWABLE PHASE CHANGE MATERIALS TRENT UNIVERSITY (CA) 2016-08-04 WO disclosed
US-20160214921-A1 LATENT HEAT STORAGE USING RENEWABLE PHASE CHANGE MATERIALS TRENT UNIVERSITY (CA) 2016-07-28 US disclosed
US-7763702-B2 Prepared by reacting a polyphosphonitrile with an amine or an alkali metal salt of an alcohol and an a perfluoroalkylsulfonylaminosulfonyl-substituted aniline or phenol salt; fuel cell membran materials THE PENN STATE RESEARCH FOUNDATION (US) 2010-07-27 US disclosed
US-20070265426-A1 Prepared by reacting a polyphosphonitrile with an amine or an alkali metal salt of an alcohol and an a perfluoroalkylsulfonylaminosulfonyl-substituted aniline or phenol salt; fuel cell membran materials THE PENN STATE RESEARCH FOUNDATION (US) 2007-11-15 US disclosed
US-20040225153-A1 Synthesis of polyphosphazenes with sulfonimide side groups THE PENN STATE RESEARCH FOUNDATION 2004-11-11 US disclosed
WO-2004072141-A2 SYNTHESIS OF POLYPHOSPHAZENES WITH SULFONIMIDE SIDE GROUPS THE PENN STATE RESEARCH FOUNDATION (US) 2004-08-26 WO disclosed