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 | |
|---|---|---|---|---|
| Potassium Ion SCHEMBL6839 | 0.89 | — | — | |
| Potassium Ion SCHEMBL14634347 | 0.80 | — | — | |
| SCHEMBL11789752 | 0.80 | — | — | |
| SCHEMBL1190396 | 0.80 | — | — | |
| Potassium Ion SCHEMBL339434 | 0.80 | — | — | |
| Potassium Ion SCHEMBL4350561 | 0.80 | — | — | |
| SCHEMBL11791491 | 0.80 | — | — | |
| Potassium Ion SCHEMBL2955595 | 0.73 | — | — | |
| Methyl Alcohol SCHEMBL1797215 | 0.73 | — | — | |
| SCHEMBL25254193 | 0.67 | — | — |
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 35 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117510332-A | New method for synthesizing 6, 8-dichloro octanoic acid ester | 风火轮(上海)生物科技有限公司 | 2024-02-06 | — | — | CN | claimed |
| CN-117088555-A | Device and method for preprocessing reactive liquid hazardous waste by utilizing microchannel reactor | 光大绿色环保危废处置(临沭)有限公司 | 2023-11-21 | — | — | CN | claimed |
| CN-116903500-A | Method for synthesizing p-methylsulfonyl benzaldehyde | 上海颐碳化学科技有限公司 | 2023-10-20 | — | — | CN | claimed |
| CN-116396205-A | N-aryl indole derivative and preparation method and application thereof | 沈阳药科大学 | 2023-07-07 | — | — | CN | claimed |
| EP-1848720-A1 | RAPID RESOLUTION PROCESS FOR CLOPIDOGREL BASE AND A PROCESS FOR PREPARATION OF CLOPIDOGREL BISULFATE POLYMORPH - FORM I | USV LIMITED (IN) | 2007-10-31 | — | — | EP | claimed |
| WO-2006087729-A1 | RAPID RESOLUTION PROCESS FOR CLOPIDOGREL BASE AND A PROCESS FOR PREPARATION OF CLOPIDOGREL BISULFATE POLYMORPH - FORM I | USV LIMITED (IN) | 2006-08-24 | — | — | WO | claimed |
| US-20060074242-A1 | Rapid resolution process of clopidogrel base and a process for preparation of clopidogrel bisulfate polymorph-form I | USV LIMITED (IN) | 2006-04-06 | — | — | US | claimed |
| CN-117510332-A | New method for synthesizing 6, 8-dichloro octanoic acid ester | 风火轮(上海)生物科技有限公司 | 2024-02-06 | — | — | CN | disclosed |
| US-20240018491-A1 | Purified Immobilized Lipases | ENZYMOCORE LTD. (IL) | 2024-01-18 | — | — | US | disclosed |
| CN-117088555-A | Device and method for preprocessing reactive liquid hazardous waste by utilizing microchannel reactor | 光大绿色环保危废处置(临沭)有限公司 | 2023-11-21 | — | — | CN | disclosed |
| CN-116903500-A | Method for synthesizing p-methylsulfonyl benzaldehyde | 上海颐碳化学科技有限公司 | 2023-10-20 | — | — | CN | disclosed |
| EP-4256042-A1 | PURIFIED IMMOBILIZED LIPASES | Enzymocore Ltd. (IL) | 2023-10-11 | — | — | EP | disclosed |
| CN-116396205-A | N-aryl indole derivative and preparation method and application thereof | 沈阳药科大学 | 2023-07-07 | — | — | CN | disclosed |
| US-6800759-B2 | REACTING MIXTURE OF (R) AND (S) CLOPIDOGREL FREE BASE WITH LEVOROTATORY CAMPHORSULFONIC ACID IN C5 TO C12 HYDROCARBON TO PRECIPITATE (S) CLOPIDOGREL CAMPHORSULFONATE, CONVERTING TO FREE BASE, PRECIPITATING CLOPIDOGREL BISULFATE IN SOLVENT | TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) | 2004-10-05 | — | — | US | disclosed |
| US-6737411-B2 | CRYSTALLIZING AS CAMPHOR SULFONATE SALT; CONVERTING PURIFIED MATERIAL BACK TO FREE BASE FORM | TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) | 2004-05-18 | — | — | US | disclosed |
| WO-2004013147-A1 | RACEMIZATION AND ENANTIOMER SEPARATION OF CLOPIDOGREL | TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) | 2004-02-12 | — | — | WO | disclosed |
| US-20040024012-A1 | Racemization and enantiomer separation of clopidogrel | TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) | 2004-02-05 | — | — | US | disclosed |
| US-20040024011-A1 | RACEMIZATION AND ENANTIOMER SEPARATION OF CLOPIDOGREL | TEVA PHARMACEUTICALS USA, INC. | 2004-02-05 | — | — | US | disclosed |
| US-5446159-A | Process for preparing imidazopyridine derivatives | LONZA, LTD. (CH) | 1995-08-29 | — | — | US | disclosed |
| US-5446160-A | Process for preparing imidazopyridine derivatives | LONZA LTD. (CH) | 1995-08-29 | — | — | US | disclosed |