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 18)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA12 | O43570 | 3/20 | 0.37 |
| ▸ | CA1 | P00915 | 3/20 | 0.37 |
| ▸ | CA9 | Q16790 | 3/20 | 0.37 |
| ▸ | CA2 | P00918 | 1/20 | 0.37 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.34 |
| ▸ | ALDH2 | P05091 | 1/20 | 0.34 |
| ▸ | MMP1 | P03956 | 1/20 | 0.32 |
| ▸ | MMP2 | P08253 | 1/20 | 0.32 |
| ▸ | MMP3 | P08254 | 1/20 | 0.32 |
| ▸ | MMP8 | P22894 | 1/20 | 0.32 |
| ▸ | PLA2G1B | P04054 | 1/20 | 0.31 |
| ▸ | PLA2G2A | P14555 | 1/20 | 0.31 |
| ▸ | GAA | P10253 | 1/20 | 0.31 |
| ▸ | HPGD | P15428 | 1/20 | 0.31 |
| ▸ | DNM1 | Q05193 | 1/20 | 0.31 |
| ▸ | MGLL | Q99685 | 1/20 | 0.30 |
| ▸ | LMNA | P02545 | 1/20 | 0.30 |
| ▸ | TSHR | P16473 | 1/20 | 0.30 |
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 | |
|---|---|---|---|---|
| Iodide SCHEMBL4346703 | 1.00 | CA12 (0.37) | CA12CA1CA9CA2ALDH1A1 | |
| Bromide SCHEMBL6731553 | 0.95 | CA12 (0.37) | CA12CA1CA9CA2ALDH1A1 | |
| Iodide SCHEMBL6151762 | 0.92 | CA12 (0.39) | CA12CA1CA9CA2ALDH1A1 | |
| Iodide SCHEMBL6151440 | 0.90 | DNM1 (0.44) | CA12CA1CA9CA2PLA2G1B | |
| Bromide SCHEMBL7929786 | 0.90 | CA12 (0.32) | CA12CA1CA9CA2ALDH1A1 | |
| Bromide SCHEMBL7929788 | 0.87 | DNM1 (0.33) | CA12CA1CA9CA2PLA2G1B | |
| SCHEMBL4336559 | 0.86 | ALDH1A1 (0.39) | CA12CA1CA9CA2ALDH1A1 | |
| Hydrochloric Acid SCHEMBL3592047 | 0.86 | CA12 (0.39) | CA12CA1CA9CA2ALDH1A1 | |
| Bromide SCHEMBL6151479 | 0.86 | CA12 (0.39) | CA12CA1CA9CA2ALDH1A1 | |
| Hydrochloric Acid SCHEMBL3587494 | 0.85 | DNM1 (0.44) | CA12CA1CA9CA2PLA2G1B |
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 7 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0944564-B9 | HALOGEN EXCHANGE REACTIONS AND USES THEREOF | ALBEMARLE CORP (US) | 2005-01-19 | — | — | EP | disclosed |
| US-6455718-B1 | FOR CONTINUOUSLY RECOVERING CHLOROPENTAFLUOROBENZENE OR BROMOPENTAFLUOROBENZENE FROM VAPOR PHASE | ALBEMARLE CORPORATION | 2002-09-24 | — | — | US | disclosed |
| EP-0944564-B1 | HALOGEN EXCHANGE REACTIONS AND USES THEREOF | ALBEMARLE CORP (US) | 2002-03-20 | — | — | EP | disclosed |
| US-6241917-B1 | Halogen exchange reactions in preparing catalysts and their precursors | ALBEMARLE CORPORATION | 2001-06-05 | — | — | US | disclosed |
| US-5965781-A | PURIFYING THE CATALYST FOR IMPROVED PERFORMANCE BY DISSOLVING THE PHOSPHONIUM HALIDE IN A LIQUID CYCLIC ETHER, REMOVING THE SOLID IMPURITIES, ADDING A NONSOLVENT TO PRECIPITATE; REACTING AN ALKALI FLUORIDE AND HALO(S)BENZENE | ALBEMARLE CORPORATION (US) | 1999-10-12 | — | — | US | disclosed |
| US-5824827-A | Halogen exchange reactions | ALBEMARLE CORPORATION (US) | 1998-10-20 | — | — | US | disclosed |
| US-5789631-A | Production of perhalobenzenes | ALBEMARLE CORPORATION (US) | 1998-08-04 | — | — | US | disclosed |