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.
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL9309197 | 0.93 | CA4 (0.35) | — | |
| SCHEMBL2802372 | 0.93 | — | — | |
| Zinc Ion SCHEMBL8845852 | 0.93 | — | — | |
| SCHEMBL2805395 | 0.93 | — | — | |
| Lithium Ion SCHEMBL9861755 | 0.93 | — | — | |
| SCHEMBL10388323 | 0.93 | — | — | |
| SCHEMBL675851 | 0.93 | — | — | |
| SCHEMBL10389158 | 0.93 | — | — | |
| SCHEMBL549045 | 0.93 | — | — | |
| SCHEMBL6757052 | 0.93 | — | — |
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 14 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-6198007-B1 | REACTING 1-HALOGENO-2,4-DINITROBENZENES WITH MONO-ALKALI METAL SALTS OF SPECIFIC DIOLS | BAYER AKTIENGESELLSCHAFT (DE) | 2001-03-06 | — | — | US | claimed |
| US-4192820-A | Preparation of 3-methyl-2-buten-1-al | BASF AKTIENGESELLSCHAFT (DE) | 1980-03-11 | — | — | US | claimed |
| EP-4655342-A1 | PROCESS FOR DEPOLYMERIZATION OF POLYALKYLENE TEREPHTHALATES IN AN EXTRUDER | Evonik Operations GmbH (DE) | 2025-12-03 | — | — | EP | disclosed |
| EP-4504401-A1 | IMPROVED METHOD FOR THE DEPOLYMERIZATION OF POLYETHYLENE TEREPHTHALATE | Evonik Operations GmbH (DE) | 2025-02-12 | — | — | EP | disclosed |
| WO-2024156568-A1 | PROCESS FOR DEPOLYMERIZATION OF POLYALKYLENE TEREPHTHALATES IN AN EXTRUDER | EVONIK OPERATIONS GMBH (DE) | 2024-08-02 | — | — | WO | disclosed |
| WO-2023193941-A1 | IMPROVED METHOD FOR THE DEPOLYMERIZATION OF POLYETHYLENE TEREPHTHALATE | EVONIK OPERATIONS GMBH (DE) | 2023-10-12 | — | — | WO | disclosed |
| US-6198007-B1 | REACTING 1-HALOGENO-2,4-DINITROBENZENES WITH MONO-ALKALI METAL SALTS OF SPECIFIC DIOLS | BAYER AKTIENGESELLSCHAFT (DE) | 2001-03-06 | — | — | US | disclosed |
| EP-0087712-B1 | METHOD FOR THE PREPARATION OF 3-CYANO-2-ALKYL ALKANALS AND USE OF 3-CYANO-2-ETHYL HEXANAL IN THE PREPARATION OF 2-PROPYLPENTANOIC ACID | BASF Aktiengesellschaft (DE) | 1986-05-07 | — | — | EP | disclosed |
| US-4410465-A | Preparation of butadiene dinitriles | BASF AKTIENGESELLSCHAFT (DE) | 1983-10-18 | — | — | US | disclosed |
| EP-0087712-A1 | Method for the preparation of 3-cyano-2-alkyl alkanals and use of 3-cyano-2-ethyl hexanal in the preparation of 2-propylpentanoic acid | BASF Aktiengesellschaft (DE) | 1983-09-07 | — | — | EP | disclosed |
| US-4219499-A | INTERMEDIATES FOR HERBICIDES, DYES AND ANTICARCINOGENS | BASF AKTIENGESELLSCHAFT (DE) | 1980-08-26 | — | — | US | disclosed |
| US-4195167-A | CONTROLLING RATIO OF PRIMARY TO SECONDARY HYDROXYL TERMINAL GROUPS IN POLYETHER | UNION CARBIDE CORPORATION (US) | 1980-03-25 | — | — | US | disclosed |
| US-4165342-A | BY OXIDATIVE DEHYDROGENATION OF THE ALCOHOL, LAYERS OF SILVER AND COPPER CATALYST CRYSTALS | BASF AKTIENGESELLSCHAFT (DE) | 1979-08-21 | — | — | US | disclosed |
| US-4131620-A | ETHERIFICATION OF N-(2-HALOALKYL)-SULFAMIC ACID HALIDES | BASF AKTIENGESELLSCHAFT (DE) | 1978-12-26 | — | — | US | disclosed |