Potassium Ion

Potassium Ion

SCHEMBL2320181

CC(C)(C)OC(=O)CC(=O)[O-].[K+]

nearest known ligand 0.41

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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 19)

geneUniProtsupporting neighboursconfidence
CA4 P22748 2/20 0.41
DGAT1 O75907 1/20 0.38
CYP2D6 P10635 1/20 0.37
CA2 P00918 3/20 0.35
CA12 O43570 3/20 0.35
CA14 Q9ULX7 2/20 0.35
TDP1 Q9NUW8 1/20 0.34
CA1 P00915 3/20 0.33
CA7 P43166 2/20 0.33
HDAC3 O15379 1/20 0.33
HDAC1 Q13547 1/20 0.33
HDAC2 Q92769 1/20 0.33
HDAC8 Q9BY41 1/20 0.33
HDAC6 Q9UBN7 1/20 0.33
MEN1 O00255 1/20 0.32
GAA P10253 1/20 0.32
KMT2A Q03164 1/20 0.32
CA9 Q16790 1/20 0.32
APLNR P35414 1/20 0.32

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
SCHEMBL9005309 0.95 CA4 (0.41) CA4DGAT1CYP2D6CA2CA12
Lithium Ion SCHEMBL223524 0.95 CA4 (0.41) CA4DGAT1CYP2D6CA2CA12
SCHEMBL241533 0.82 DGAT1 (0.46) DGAT1CYP2D6CA2CA12CA14
Potassium Ion SCHEMBL28727566 0.80 CA4 (0.36) CA4
Methyl Alcohol SCHEMBL27995686 0.79 DGAT1 (0.44) DGAT1CYP2D6CA2CA12CA14
SCHEMBL28315778 0.77 CA4 (0.42) CA4CA2HDAC3HDAC1HDAC2
SCHEMBL28727603 0.77 CA4 (0.38) CA4
SCHEMBL2648388 0.77 DGAT1 (0.42) DGAT1CYP2D6CA2CA12CA14
SCHEMBL28316203 0.77 DGAT1 (0.42) DGAT1CYP2D6CA2CA12CA14
SCHEMBL19459343 0.76 DGAT1 (0.38) DGAT1CYP2D6CA2CA12CA14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114773335-A Preparation method of 6-halo-4-hydroxy-1, 5-naphthyridine-3-formic acid and ester thereof 内蒙古京东药业有限公司 2022-07-22 CN claimed
CN-114315746-A 3, 6-bis (dinitromethyl) -1,2,4, 5-tetrazine and synthetic method thereof 南京理工大学 2022-04-12 CN claimed
CN-109867679-B Preparation method of piricaconide hydrochloride intermediate 杭州瀚康生物医药科技有限公司 2021-11-30 CN claimed
EP-4724441-A1 ISOINDOLINONE AND DIHYDROPYRROLOPRIDINONE COMPOUNDS AND USES THEREOF Revir Therapeutics, Inc. (US) 2026-04-15 EP disclosed
EP-4695242-A1 NOVEL SUBSTITUTED PYRROLE COMPOUNDS, COMPOSITIONS COMPRISING THE SUBSTITUTED PYRROLE COMPOUND, AND METHODS OF USE THEREOF Meta Pharmaceuticals (HK) Limited (HK) 2026-02-18 EP disclosed
WO-2024251212-A1 ISOINDOLINONE AND DIHYDROPYRROLOPRIDINONE COMPOUNDS AND USES THEREOF REVIR THERAPEUTICS, INC. (US) 2024-12-12 WO disclosed
WO-2024251211-A1 COMPOSITIONS, METHODS, AND SYSTEMS FOR MODULATING SPLICING OF MSH3 REVIR THERAPEUTICS, INC. (US) 2024-12-12 WO disclosed
WO-2024212907-A1 NOVEL SUBSTITUTED PYRROLE COMPOUNDS, COMPOSITIONS COMPRISING THE SUBSTITUTED PYRROLE COMPOUND, AND METHODS OF USE THEREOF META PHARMACEUTICALS (HK) LIMITED (CN) 2024-10-17 WO disclosed
CN-111032034-B Spiro compounds and methods of making and using the same H.隆德贝克有限公司 2023-05-02 CN disclosed
CN-114315746-A 3, 6-bis (dinitromethyl) -1,2,4, 5-tetrazine and synthetic method thereof 南京理工大学 2022-04-12 CN disclosed
EP-3675848-B1 SPIROCYCLE COMPOUNDS AND METHODS OF MAKING AND USING SAME H LUNDBECK AS (DK) 2022-03-23 EP disclosed
US-5216174-A Process for trans-6-[12-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis WARNER-LAMBERT CO. (US) 1993-06-01 US disclosed
US-5149837-A Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis WARNER-LAMBERT COMPANY (US) 1992-09-22 US disclosed
US-5124482-A Process for trans-6-(2-substituted-pyrrol-1-yl)alkyl)pyran-2-one inhibitors of cholesterol synthesis WARNER-LAMBERT COMPANY (US) 1992-06-23 US disclosed
US-5097045-A Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis WARNER-LAMBERT COMPANY (US) 1992-03-17 US disclosed
US-5003080-A Process for trans-6-(2-(substituted-pyrrol-1-yl)alkyl)pryan-2-one inhibitors of cholesterol synthesis WARNER-LAMBERT COMPANY (US) 1991-03-26 US disclosed
EP-0330172-A2 Improved process for trans-6-[2-(substituted-pyrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis WARNER-LAMBERT COMPANY (US) 1989-08-30 EP disclosed
US-4375433-A ANTIBIOTICS MERCK & CO., INC. (US) 1983-03-01 US disclosed
US-4252722-A CHEMICAL INTERMEDIATE MERCK & CO., INC. (US) 1981-02-24 US disclosed
EP-0010312-A2 Process for the preparation of 6-hydroxymethyl-2-(beta-aminoethylthio)-1-carbadethiapen-2-em-3-carboxylic acid and intermediates useful in this process MERCK & CO. INC. (US) 1980-04-30 EP disclosed