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.
Predicted protein targets (top 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SMN1; SMN2 | Q16637 | 3/20 | 0.41 |
| ▸ | MEN1 | O00255 | 2/20 | 0.41 |
| ▸ | HSP90AA1 | P07900 | 2/20 | 0.41 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.41 |
| ▸ | FDPS | P14324 | 2/20 | 0.41 |
| ▸ | NPC1 | O15118 | 2/20 | 0.38 |
| ▸ | HTT | P42858 | 2/20 | 0.38 |
| ▸ | RAB9A | P51151 | 2/20 | 0.38 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.38 |
| ▸ | LMNA | P02545 | 1/20 | 0.38 |
| ▸ | APAF1 | O14727 | 1/20 | 0.38 |
| ▸ | PLA2G1B | P04054 | 1/20 | 0.38 |
| ▸ | MAPT | P10636 | 1/20 | 0.38 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.38 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.38 |
| ▸ | ATG4B | Q9Y4P1 | 1/20 | 0.38 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL372519 | 0.98 | MEN1 (0.42) | SMN1; SMN2MEN1HSP90AA1KMT2AFDPS | |
| Bromide SCHEMBL5168946 | 0.96 | MEN1 (0.45) | SMN1; SMN2MEN1HSP90AA1KMT2AFDPS | |
| Hydrochloric Acid SCHEMBL961160 | 0.96 | MEN1 (0.41) | SMN1; SMN2MEN1HSP90AA1KMT2AFDPS | |
| Fluoride Ion SCHEMBL5172541 | 0.96 | MEN1 (0.41) | SMN1; SMN2MEN1HSP90AA1KMT2AFDPS | |
| Iodide SCHEMBL28929886 | 0.92 | SMN1; SMN2 (0.48) | SMN1; SMN2MEN1HSP90AA1KMT2ANPC1 | |
| Iodide SCHEMBL11535780 | 0.92 | SMN1; SMN2 (0.48) | SMN1; SMN2MEN1HSP90AA1KMT2ANPC1 | |
| SCHEMBL899200 | 0.92 | ABCB11 (0.45) | SMN1; SMN2MEN1HSP90AA1KMT2A | |
| SCHEMBL17699216 | 0.91 | MEN1 (0.39) | SMN1; SMN2MEN1HSP90AA1KMT2AFDPS | |
| SCHEMBL7516471 | 0.91 | MEN1 (0.39) | SMN1; SMN2MEN1HSP90AA1KMT2AFDPS | |
| SCHEMBL28333445 | 0.91 | MEN1 (0.39) | SMN1; SMN2MEN1HSP90AA1KMT2AFDPS |
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 33 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2790197-A2 | Electrolyte for dye sensitized solar cell and dye sensitized solar cell using the same | Samsung SDI Co., Ltd. (KR) | 2014-10-15 | — | — | EP | claimed |
| US-20140299190-A1 | ELECTROLYTE FOR DYE SENSITIZED SOLAR CELL AND DYE SENSITIZED SOLAR CELL USING THE SAME | SAMSUNG SDI CO., LTD. (KR) | 2014-10-09 | — | — | US | claimed |
| US-20110100461-A1 | ELECTROLYTE COMPOSITION AND DYE-SENSITIZED SOLAR CELL HAVING THE SAME | EVERLIGHT USA, INC. (US) | 2011-05-05 | — | — | US | claimed |
| US-20110100464-A1 | Electrolyte composition and dye-sensitized solar cell using the same | EVERLIGHT USA, INC. (US) | 2011-05-05 | — | — | US | claimed |
| EP-1663921-B1 | METHOD FOR PRODUCING HALOALKANES FROM ALCOHOLS | BASF AG (DE) | 2007-05-02 | — | — | EP | claimed |
| US-20070055084-A1 | Method for producing haloalkanes from alcohols | BASF AKTIENGESELLSCHAFT (DE) | 2007-03-08 | — | — | US | claimed |
| US-12540715-B2 | Lighting diffuser plate for collecting and recycling light energy, and lighting apparatus system comprising same | DONGGUK UNIVERSITY INDUSTRY-ACADEMIC COOPERATION FOUNDATION (KR) | 2026-02-03 | — | — | US | disclosed |
| US-20250216053-A1 | LIGHTING DIFFUSER PLATE FOR COLLECTING AND RECYCLING LIGHT ENERGY, AND LIGHTING APPARATUS SYSTEM COMPRISING SAME | DONGGUK UNIVERSITY INDUSTRY-ACADEMIC COOPERATION FOUNDATION (KR) | 2025-07-03 | — | — | US | disclosed |
| WO-2023048350-A1 | LIGHTING DIFFUSER PLATE FOR COLLECTING AND RECYCLING LIGHT ENERGY, AND LIGHTING APPARATUS SYSTEM COMPRISING SAME | 동국대학교 산학협력단 | 2023-03-30 | — | — | WO | disclosed |
| WO-2022118948-A1 | METHOD FOR VISUALIZING GAPS IN SAMPLE | 国立研究開発法人海洋研究開発機構 | 2022-06-09 | — | — | WO | disclosed |
| EP-2790197-A2 | Electrolyte for dye sensitized solar cell and dye sensitized solar cell using the same | Samsung SDI Co., Ltd. (KR) | 2014-10-15 | — | — | EP | disclosed |
| US-20140299190-A1 | ELECTROLYTE FOR DYE SENSITIZED SOLAR CELL AND DYE SENSITIZED SOLAR CELL USING THE SAME | SAMSUNG SDI CO., LTD. (KR) | 2014-10-09 | — | — | US | disclosed |
| US-20140291166-A1 | METHOD AND KIT FOR ELECTROCHEMICALLY DETECTING ANALYTE | SYSMEX CORPORATION (JP) | 2014-10-02 | — | — | US | disclosed |
| US-7629491-B2 | Hydrocarboxylation process | EASTMAN CHEMICAL COMPANY (US) | 2009-12-08 | — | — | US | disclosed |
| US-20090061315-A1 | Nonaqueous electrolyte battery | KABUSHIKI KAISHA TOYOTA CHUO KENKYUSHO (JP) | 2009-03-05 | — | — | US | disclosed |
| US-20080112866-A1 | Functionalized ionic liquids, and methods of use thereof | UNIVERSITY OF SOUTH ALABAMA (US) | 2008-05-15 | — | — | US | disclosed |
| US-20070299280-A1 | forming propionic acid from ethylene, water and carbon monoxide; not using the hazardous and corrosive hydrogen halides or sulfonic acids; free of hydrogen iodide and/or ethyl iodide; no diethyl ketone by-products | EASTMAN CHEMICAL COMPANY (US) | 2007-12-27 | — | — | US | disclosed |
| US-7208605-B2 | Functionalized ionic liquids, and methods of use thereof | UNIVERSITY OF SOUTH ALABAMA (US) | 2007-04-24 | — | — | US | disclosed |
| US-20070055084-A1 | Method for producing haloalkanes from alcohols | BASF AKTIENGESELLSCHAFT (DE) | 2007-03-08 | — | — | US | disclosed |
| US-20040035293-A1 | Functionalized ionic liquids, and methods of use thereof | UNIVERSITY OF SOUTH ALABAMA | 2004-02-26 | — | — | US | 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 (5 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20070299280-A1 | forming propionic acid from ethylene, water and carbon monoxide; not using the hazardous and corrosive hydrogen halides or sulfonic acids; free of hydrogen iodide and/or ethyl iodide; no diethyl ketone by-products | ETV6, ETV1, HAO2 | SMN1; SMN2 3854/4885MEN1 2978/4885HSP90AA1 1214/4885 |
| US-20070055084-A1 | Method for producing haloalkanes from alcohols | ADH1C, HDHD5, ADH5 | SMN1; SMN2 4795/4885MEN1 4351/4885HSP90AA1 364/4885 |
| US-12540715-B2 | Lighting diffuser plate for collecting and recycling light energy, and lighting apparatus system comprising same | SOD1, SLC30A7, SLC39A7 | SMN1; SMN2 3677/4885MEN1 613/4885HSP90AA1 4260/4885 |
| US-20040035293-A1 | Functionalized ionic liquids, and methods of use thereof | TST, SCLY, MPST | SMN1; SMN2 1737/4885MEN1 2015/4885HSP90AA1 4683/4885 |
| US-20080112866-A1 | Functionalized ionic liquids, and methods of use thereof | TST, SCLY, MPST | SMN1; SMN2 1737/4885MEN1 2015/4885HSP90AA1 4683/4885 |
“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.