Potassium Ion

Potassium Ion

SCHEMBL5080002

CCOC(=O)C(C)C(=O)[O-].[K+]

nearest known ligand 0.42

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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
ALDH1A1 P00352 4/20 0.42
HPGD P15428 1/20 0.41
LMNA P02545 2/20 0.40
HSD17B10 Q99714 1/20 0.40
ALOX15 P16050 1/20 0.39
MGAM O43451 1/20 0.39
GAA P10253 1/20 0.39
SI P14410 1/20 0.39
MGAM2 Q2M2H8 1/20 0.39
SOAT1 P35610 1/20 0.39
CYP3A4 P08684 2/20 0.36
TSHR P16473 2/20 0.36
NFKB1 P19838 2/20 0.36
NPSR1 Q6W5P4 2/20 0.36
TRPA1 O75762 1/20 0.36
CA1 P00915 2/20 0.35
PIN1 Q13526 1/20 0.33
METAP2 P50579 1/20 0.33
METAP1 P53582 1/20 0.33

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
Potassium Ion SCHEMBL29874034 1.00 ALDH1A1 (0.42) ALDH1A1HPGDLMNAHSD17B10ALOX15
Lithium Ion SCHEMBL30033845 0.95 ALDH1A1 (0.42) ALDH1A1HPGDLMNAHSD17B10ALOX15
SCHEMBL141446 0.82 ALDH1A1 (0.53) ALDH1A1HPGDLMNAHSD17B10ALOX15
SCHEMBL8800602 0.79 ALDH1A1 (0.50) ALDH1A1HPGDLMNAHSD17B10ALOX15
Ethane SCHEMBL9181718 0.79 ALDH1A1 (0.50) ALDH1A1HPGDLMNAHSD17B10ALOX15
Ammonia Solution, Strong SCHEMBL28791130 0.79 ALDH1A1 (0.50) ALDH1A1HPGDLMNAHSD17B10ALOX15
SCHEMBL28186389 0.79 ALDH1A1 (0.50) ALDH1A1HPGDLMNAHSD17B10ALOX15
SCHEMBL5143571 0.77 ALDH1A1 (0.48) ALDH1A1HPGDLMNAHSD17B10ALOX15
SCHEMBL41804 0.75 ALDH1A1 (0.50) ALDH1A1HPGDLMNAHSD17B10ALOX15
SCHEMBL4112176 0.75 ALDH1A1 (0.46) ALDH1A1HPGDLMNAHSD17B10ALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024206939-A2 SARS-COV-2 ENTRY INHIBITORS UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) 2024-10-03 WO disclosed
EP-3884939-B1 3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF RAZE THERAPEUTICS INC (US) 2023-10-25 EP disclosed
US-20230312536-A1 3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF RAZE THERAPEUTICS, INC. 2023-10-05 US disclosed
US-11634412-B2 3-phosphoglycerate dehydrogenase inhibitors and uses thereof RAZE THERAPEUTICS, INC. (US) 2023-04-25 US disclosed
US-20230027985-A1 SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS BAYER AKTIENGESELLSCHAFT (DE) 2023-01-26 US disclosed
US-20230009122-A1 3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF RAZE THERAPEUTICS, INC. 2023-01-12 US disclosed
EP-4058446-A1 SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS Bayer Aktiengesellschaft (DE) 2022-09-21 EP disclosed
EP-3884939-A1 3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF Raze Therapeutics, Inc. (US) 2021-09-29 EP disclosed
WO-2021094434-A1 SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS BAYER AKTIENGESELLSCHAFT (DE) 2021-05-20 WO disclosed
EP-3426243-B1 3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF RAZE THERAPEUTICS INC (US) 2021-05-19 EP disclosed
EP-1334976-A1 Novel phosphine compound, transition metal complex containing said compound as ligand and asymetric synthesis catalyst containing said complex Takasago International Corporation (JP) 2003-08-13 EP disclosed
US-20030144139-A1 Novel phosphine compound, transition metal complex containing the same phosphine compound as ligand and asymmetric synthesis catalyst containing the complex TAKASAGO INTERNATIONAL CORPORATION (JP) 2003-07-31 US disclosed
US-6548695-B2 Immunoregulation MERCIAN CORPORATION (JP) 2003-04-15 US disclosed
US-20020147350-A1 Process for producing isocoumarins and intermediates for the same TSUCHIDA TOSHIO (JP) 2002-10-10 US disclosed
US-6426420-B1 REACTING A HOMOPHTHALIC ACID DERIVATIVE WITH A MALONIC ACID DERIVATINE MERCIAN CORPORATION (JP) 2002-07-30 US disclosed
EP-1200421-A1 PROCESS FOR PRODUCING ISOCOUMARINS AND INTERMEDIATES FOR THE SAME MERCIAN CORPORATION (JP) 2002-05-02 EP disclosed
EP-0749964-B1 N-Heterocyclyl biphenyl sulfonamides ASTRAZENECA AB (SE) 2001-10-04 EP disclosed
WO-2001007429-A1 PROCESS FOR PRODUCING ISOCOUMARINS AND INTERMEDIATES FOR THE SAME MERCIAN CORPORATION (JP) 2001-02-01 WO disclosed
US-5668137-A N-heterocyclic sulfonamides having endothelin receptor activity ZENECA LTD. (GB) 1997-09-16 US disclosed
EP-0749964-A1 N-Heterocyclyl biphenyl sulfonamides ZENECA LIMITED (GB) 1996-12-27 EP 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 (6 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-11634412-B2 3-phosphoglycerate dehydrogenase inhibitors and uses thereof PHGDH, G6PD, PGD ALDH1A1 222/4885HPGD 97/4885LMNA 3385/4885
US-20230027985-A1 SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS ADAMTS7, MMP7, ADAMTS1 ALDH1A1 2009/4885HPGD 599/4885LMNA 2772/4885
US-20030144139-A1 Novel phosphine compound, transition metal complex containing the same phosphine compound as ligand and asymmetric synthesis catalyst containing the complex PHOSPHO1, MEN1, PDCD1 ALDH1A1 4025/4885HPGD 3624/4885LMNA 4812/4885
US-20230009122-A1 3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF PHGDH, G6PD, PGD ALDH1A1 222/4885HPGD 97/4885LMNA 3385/4885
US-20230312536-A1 3-PHOSPHOGLYCERATE DEHYDROGENASE INHIBITORS AND USES THEREOF PHGDH, G6PD, PGD ALDH1A1 222/4885HPGD 97/4885LMNA 3385/4885
US-20020147350-A1 Process for producing isocoumarins and intermediates for the same IDH1, IDH2, ME1 ALDH1A1 241/4885HPGD 161/4885LMNA 2093/4885

“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.