Potassium Ion

Potassium Ion

SCHEMBL1890648

O=C([O-])CCCOc1ccc(Cl)cc1Cl.[K+]

nearest known ligand 0.67

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
MAPT P10636 2/20 0.67
HPGD P15428 8/20 0.62
RAB9A P51151 4/20 0.62
NPC1 O15118 3/20 0.62
TSHR P16473 2/20 0.62
SMN1; SMN2 Q16637 2/20 0.62
NLRP1 Q9C000 1/20 0.60
MAPK1 P28482 2/20 0.59
TP53 P04637 1/20 0.59
L3MBTL1 Q9Y468 1/20 0.59
CYP1A2 P05177 2/20 0.58
CYP2C19 P33261 2/20 0.58
CYP3A4 P08684 1/20 0.58
GAA P10253 1/20 0.58
ALDH1A1 P00352 3/20 0.56
LMNA P02545 1/20 0.56
MEN1 O00255 1/20 0.56
KMT2A Q03164 1/20 0.56
TDP1 Q9NUW8 1/20 0.55
HTT P42858 1/20 0.52

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
SCHEMBL5311708 0.97 MAPT (0.67) MAPTHPGDRAB9ANPC1TSHR
Potassium Ion SCHEMBL8438890 0.92 MAPT (0.60) MAPTHPGDRAB9ANPC1TSHR
SCHEMBL8441616 0.89 MAPT (0.60) MAPTHPGDRAB9ANPC1TSHR
SCHEMBL29364868 0.85 RAB9A (0.78) MAPTHPGDRAB9ANPC1TSHR
SCHEMBL116448 0.85 RAB9A (0.78) MAPTHPGDRAB9ANPC1TSHR
Mcpb SCHEMBL1896022 0.85 KDM4E (0.68) MAPTHPGDRAB9ANPC1SMN1; SMN2
SCHEMBL12522764 0.84 MAPT (0.70) MAPTHPGDRAB9ANPC1TSHR
Hydrochloric Acid SCHEMBL11002766 0.84 RAB9A (0.76) MAPTHPGDRAB9ANPC1TSHR
SCHEMBL11002763 0.84 MAPT (0.70) MAPTHPGDRAB9ANPC1TSHR
SCHEMBL8389330 0.83 MAPT (0.73) MAPTHPGDRAB9ANPC1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4337017-A1 HERBICIDE/SAFENER COMBINATION BASED ON SAFENERS FROM THE CLASS OF SUBSTITUTED [(1,5-DIPHENYL-1H-1,2,4-TRIAZOL-3-YL)OXY]ACETIC ACIDS AND THEIR SALTS Bayer Aktiengesellschaft (DE) 2024-03-20 EP claimed
WO-2022152728-A1 HERBICIDAL COMPOSITIONS BAYER AKTIENGESELLSCHAFT (DE) 2022-07-21 WO claimed
EP-4601471-A1 SUBSTITUTED 5-MEMBERED RINGS AND THEIR USE AS PESTICIDES Corteva Agriscience LLC (US) 2025-08-20 EP disclosed
WO-2025128414-A1 TRANSGENIC SOYBEAN EVENT GM_CSM63717 AND COMPOSITIONS AND METHODS FOR DETECTION AND USES THEREOF MONSANTO TECHNOLOGY LLC (US) 2025-06-19 WO disclosed
WO-2025103939-A1 SULFONIMIDOYL BENZAMIDES WITH HERBICIDAL ACTION BAYER AKTIENGESELLSCHAFT (DE) 2025-05-22 WO disclosed
CN-115024314-B Agricultural chemical composition 巴特尔英国有限公司 2025-05-09 CN disclosed
CN-119546187-A Method for controlling undesired plants and promoting growth of useful plants 石原产业株式会社 2025-02-28 CN disclosed
WO-2024209996-A1 METHOD FOR CONTROLLING HERBICIDE-RESISTANT WEEDS 住友化学株式会社 2024-10-10 WO disclosed
CN-118632626-A (1, 4, 5-Trisubstituted-1H-pyrazol-3-yl) oxy-2-alkoxythioalkyl acids and derivatives thereof, salts thereof and use thereof as herbicidal agents 拜耳公司 2024-09-10 CN disclosed
EP-4378314-A2 HERBICIDAL COMPOSITIONS Bayer AG (DE) 2024-06-05 EP disclosed
CN-107846894-B Herbicidal composition comprising clomazone and a specific photosystem II inhibitor 巴斯夫农业公司 2024-05-28 CN disclosed
US-20040069033-A1 Controlled release products and processes for the preparation thereof OMS INVESTMENTS, INC. 2004-04-15 US disclosed
EP-1370135-A1 CONTROLLED RELEASE PRODUCTS AND PROCESSES FOR THE PREPARATION THEREOF OMS Investments, Inc. (US) 2003-12-17 EP disclosed
US-6656882-B2 Coated products in particulate form which are structured to provide release profiles wherein initial release of active ingredients such as fertilizer nutrients is suppressed or for predetermined period and longevity for release within 60 days OMS INVESTMENTS, INC. 2003-12-02 US disclosed
US-20020168318-A1 Controlled release products and processes for the preparation thereof OMS INVESTMENTS, INC. 2002-11-14 US disclosed
WO-2002068363-A2 CONTROLLED RELEASE PRODUCTS AND PROCESSES FOR THE PREPARATION THEREOF OMS INVESTMENTS, INC. (US) 2002-09-06 WO disclosed
EP-0628527-B1 Timed release of water-soluble plant nutrients OMS INVESTMENTS INC (US) 2001-04-11 EP disclosed
US-5652196-A Timed release of water-soluble plant nutrients OMS INVESTMENTS, INC. (US) 1997-07-29 US disclosed
EP-0628527-A1 Timed release of water-soluble plant nutrients W.R. Grace & Co.-Conn. (US) 1994-12-14 EP disclosed
US-4015970-A FERTILIZER WITH POLYMERIC COATING AIRWICK INDUSTRIES, INC. (US) 1977-04-05 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-20040069033-A1 Controlled release products and processes for the preparation thereof GHITM, LBR, VMA21 MAPT 246/4885HPGD 679/4885RAB9A 2158/4885

“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.