Known targets — ChEMBL curated mechanism
ACHECHRM1CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNG
The experimentally established mechanism targets of Iodide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| Bromide SCHEMBL10424808 | 0.94 | — | — | |
| SCHEMBL6355112 | 0.67 | — | — | |
| SCHEMBL9935822 | 0.65 | — | — | |
| SCHEMBL9934781 | 0.65 | — | — | |
| SCHEMBL9936381 | 0.61 | — | — | |
| Iodide SCHEMBL6847392 | 0.60 | — | — | |
| SCHEMBL666807 | 0.47 | — | — | |
| Iodide SCHEMBL698825 | 0.35 | — | — | |
| Iodide SCHEMBL431450 | 0.35 | — | — | |
| Iodide SCHEMBL489610 | 0.35 | — | — |
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 168 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20180340001-A1 | Probes for 18F Positron Emission Tomography Imaging | NIH-DEITR | 2018-11-29 | — | — | US | claimed |
| US-20110056563-A1 | ELECTROLYTE COMPOSITION | SOLARPRINT LIMITED (IE) | 2011-03-10 | — | — | US | claimed |
| EP-2250657-A1 | ELECTROLYTE COMPOSITION | Solarprint Limited (IE) | 2010-11-17 | — | — | EP | claimed |
| WO-2009103970-A1 | ELECTROLYTE COMPOSITION | SOLARPRINT LIMITED (IE) | 2009-08-27 | — | — | WO | claimed |
| EP-0476333-B1 | Process for simultaneous production of acetic acid and acetanhydride | HOECHST AG (DE) | 1994-11-30 | — | — | EP | claimed |
| US-4853482-A | ISOMERIZATION OF ESTER USING CARBON MOOXIDE AND GROUP 8 METAL AND GROUP 5 METAL QUATERNARY CATALYST | BP CHEMICALS LIMITED (GB) | 1989-08-01 | — | — | US | claimed |
| US-4333884-A | Production of acetic anhydride | HOECHST AKTIENGESELLSCHAFT (DE) | 1982-06-08 | — | — | US | claimed |
| US-4319038-A | BY REACTING METHYL ACETATE OR DIMETHYL ETHER WITH CARBON MONOXIDE AND HYDROGEN IN THE PRESENCE OF A CATALYST SYSTEM WHICH INCLUDES AN ALIPHATIC CARBOXYLIC ACID, A MANGANESE OR RHEMIUM COMPOUND, AND A HETEROCYCLIC NITROGEN-CONTAINING SALT | HOECHST AKTIENGESELLSCHAFT (DE) | 1982-03-09 | — | — | US | claimed |
| JP-5331095-A | — | — | None | — | — | JP | disclosed |
| EP-2892106-B1 | DYE-SENSITIZED SOLAR CELL ELEMENT FOR LOW LUMINANCE | FUJIKURA LTD (JP) | 2022-05-04 | — | — | EP | disclosed |
| EP-2645459-B1 | Substrate and secondary battery | TOSHIBA KK (JP) | 2022-02-09 | — | — | EP | disclosed |
| US-11028097-B2 | Thienopyrimidine compounds | VERNALIS (R&D) LIMITED (GB) | 2021-06-08 | — | — | US | disclosed |
| US-10692658-B2 | Photoelectric conversion element | FUJIKURA LTD. (JP) | 2020-06-23 | — | — | US | disclosed |
| CN-108231422-B | Photoelectric conversion element and electronic component having the same | 太阳诱电株式会社 | 2020-06-23 | — | — | CN | disclosed |
| US-4440570-A | Process for purifying and recovering contaminated catalyst solution obtained in the carbonylation of methyl acetate and/or dimethylether | HOECHST AKTIENGESELLSCHAFT (DE) | 1984-04-03 | — | — | US | disclosed |
| US-4430273-A | Production of acetic anhydride | HOECHST AKTIENGESELLSCHAFT (DE) | 1984-02-07 | — | — | US | disclosed |
| EP-0098689-A1 | Process for the production of monocarboxylic acid anhydrides | BP Chemicals Limited (GB) | 1984-01-18 | — | — | EP | disclosed |
| US-4351972-A | Process for making anhydrous alkyl iodides | HOECHST AKTIENGESELLSCHAFT (DE) | 1982-09-28 | — | — | US | disclosed |
| US-4333884-A | Production of acetic anhydride | HOECHST AKTIENGESELLSCHAFT (DE) | 1982-06-08 | — | — | US | disclosed |
| US-4319038-A | BY REACTING METHYL ACETATE OR DIMETHYL ETHER WITH CARBON MONOXIDE AND HYDROGEN IN THE PRESENCE OF A CATALYST SYSTEM WHICH INCLUDES AN ALIPHATIC CARBOXYLIC ACID, A MANGANESE OR RHEMIUM COMPOUND, AND A HETEROCYCLIC NITROGEN-CONTAINING SALT | HOECHST AKTIENGESELLSCHAFT (DE) | 1982-03-09 | — | — | US | disclosed |