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 | |
|---|---|---|---|---|
| Iodide SCHEMBL11870879 | 1.00 | SLC22A2 (0.45) | — | |
| Iodide SCHEMBL28719356 | 1.00 | SLC22A2 (0.45) | — | |
| Phosphine SCHEMBL28180262 | 1.00 | — | — | |
| Iodide SCHEMBL28797980 | 1.00 | SLC22A2 (0.45) | — | |
| Ammonia Solution, Strong SCHEMBL27995565 | 0.96 | — | — | |
| Iodide SCHEMBL28191685 | 0.96 | — | — | |
| Iodide SCHEMBL27999159 | 0.96 | — | — | |
| Iodide SCHEMBL11870886 | 0.96 | SLC22A2 (0.43) | — | |
| Iodide SCHEMBL17431666 | 0.96 | SLC22A2 (0.43) | — | |
| Iodide SCHEMBL27844053 | 0.96 | — | — |
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 694 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2025034753-A1 | CATALYTIC CARBONYLATION OF ESTERS | THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) | 2025-02-13 | — | — | WO | claimed |
| US-12163961-B2 | BTEX metabolites derivatization kit and composition | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 2024-12-10 | — | — | US | claimed |
| EP-4408821-A1 | CATALYTIC METHODS FOR CARBONYLATION OF ESTERS | The University of North Carolina at Chapel Hill (US) | 2024-08-07 | — | — | EP | claimed |
| CN-118284590-A | Catalytic process for carbonylation of esters | 北卡罗来纳大学教堂山分校 | 2024-07-02 | — | — | CN | claimed |
| CN-116925046-A | Pyridine cation mitochondrial fluorescent probe and preparation and application thereof | 山东大学深圳研究院 | 2023-10-24 | — | — | CN | claimed |
| WO-2023049476-A1 | CATALYTIC METHODS FOR CARBONYLATION OF ESTERS | THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) | 2023-03-30 | — | — | WO | claimed |
| US-20230069226-A1 | BTEX METABOLITES DERIVATIZATION KIT AND COMPOSITION | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM | 2023-03-02 | — | — | US | claimed |
| US-11506669-B2 | BTEX metabolites derivatization kit and composition | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 2022-11-22 | — | — | US | claimed |
| US-11248260-B2 | Quantitative amplification normalization with quenchers | BIO-RAD LABORATORIES, INC. (US) | 2022-02-15 | — | — | US | claimed |
| CN-110452199-A | A kind of preparation method of Fei Luokao former times | SHANDONG LUKANG SHELILE PHARMACEUTICAL CO LTD | 2019-11-15 | — | — | CN | claimed |
| US-20040176327-A1 | Use of bisphosphonic acids for treating angiogenesis | NOVARTIS AG (CH) | 2004-09-09 | — | — | US | claimed |
| EP-0458502-B1 | Latent catalysts, cure-inhibited epoxy resin compositions and laminates prepared therefrom | DOW GLOBAL TECHNOLOGIES INC (US) | 2003-06-18 | — | — | EP | claimed |
| EP-0476333-B1 | Process for simultaneous production of acetic acid and acetanhydride | HOECHST AG (DE) | 1994-11-30 | — | — | EP | claimed |
| US-5169473-A | Complex of an onium, arsenic or amine compound and boric acid; advanced polyepoxides; storage stability | THE DOW CHEMICAL COMPANY (US) | 1992-12-08 | — | — | US | claimed |
| EP-0458502-A2 | Latent catalysts, cure-inhibited epoxy resin compositions and laminates prepared therefrom | THE DOW CHEMICAL COMPANY (US) | 1991-11-27 | — | — | EP | 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 |
| US-4174396-A | REACTING 3-THIENYLMAGNESIUM BROMIDE AND N-METHYLPYRIDINIUM IODIDE, ACIDIFICATION, ANALGESICS | LABORATORIES MADE, S.A. (ES) | 1979-11-13 | — | — | US | claimed |
| US-4067882-A | REACTING DIALKOXY-PHOSPHINYL-DITHIOCARBAMATE WITH METHYLENE HALIDE | AMERICAN CYANAMID COMPANY (US) | 1978-01-10 | — | — | US | claimed |
| US-3957517-A | Dry stabilization of a silver halide photographic material | FUJI PHOTO FILM CO., LTD. (JA) | 1976-05-18 | — | — | US | claimed |