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 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA2 | P00918 | 2/20 | 0.45 |
| ▸ | CA4 | P22748 | 2/20 | 0.45 |
| ▸ | CA5A | P35218 | 1/20 | 0.45 |
| ▸ | ESR1 | P03372 | 3/20 | 0.39 |
| ▸ | ESR2 | Q92731 | 2/20 | 0.39 |
| ▸ | CFTR | P13569 | 1/20 | 0.39 |
| ▸ | ALDH1A1 | P00352 | 6/20 | 0.38 |
| ▸ | L3MBTL1 | Q9Y468 | 3/20 | 0.38 |
| ▸ | TDP1 | Q9NUW8 | 3/20 | 0.38 |
| ▸ | ALOX12 | P18054 | 2/20 | 0.38 |
| ▸ | GAA | P10253 | 2/20 | 0.38 |
| ▸ | HTT | P42858 | 2/20 | 0.38 |
| ▸ | MAPT | P10636 | 1/20 | 0.38 |
| ▸ | ALPG | P10696 | 1/20 | 0.38 |
| ▸ | NPY1R | P25929 | 1/20 | 0.38 |
| ▸ | NPY2R | P49146 | 1/20 | 0.38 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.38 |
| ▸ | ALOX15 | P16050 | 2/20 | 0.37 |
| ▸ | TSHR | P16473 | 2/20 | 0.37 |
| ▸ | PTGS1 | P23219 | 1/20 | 0.37 |
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 | |
|---|---|---|---|---|
| SCHEMBL2932036 | 0.96 | CA2 (0.47) | CA2CA4CA5AESR1ESR2 | |
| SCHEMBL29183480 | 0.92 | CA2 (0.45) | CA2CA4CA5AESR1ESR2 | |
| SCHEMBL22470753 | 0.92 | CA2 (0.45) | CA2CA4CA5AESR1ESR2 | |
| Hydrochloric Acid SCHEMBL28961494 | 0.92 | CA2 (0.45) | CA2CA4CA5AESR1ESR2 | |
| SCHEMBL29008512 | 0.83 | CA2 (0.39) | CA2CA4CA5AESR1ESR2 | |
| Iodide SCHEMBL27336456 | 0.79 | CA2 (0.41) | CA2CA4CA5AESR1ESR2 | |
| Iodide SCHEMBL3694471 | 0.79 | CA2 (0.41) | CA2CA4CA5AESR1ESR2 | |
| Fluorobenzene SCHEMBL27277602 | 0.78 | NFE2L2 (0.39) | CA2CA4CA5AESR1ESR2 | |
| Bromide SCHEMBL27278868 | 0.76 | NFE2L2 (0.42) | CA2CA4CA5AESR1ESR2 | |
| SCHEMBL361668 | 0.74 | CA2 (0.43) | CA2CA4CA5AESR1ESR2 |
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 16 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118813253-A | Preparation method of tin-based perovskite | 南京工业大学 | 2024-10-22 | — | — | CN | claimed |
| CN-117758369-A | Zero-dimensional silver-based organic-inorganic hybrid metal halide single crystal material, and preparation method and application thereof | 重庆邮电大学 | 2024-03-26 | — | — | CN | claimed |
| CN-113735901-A | Preparation method of tetraphenyl phosphorus iodide | 西安思科赛实业有限公司 | 2021-12-03 | — | — | CN | claimed |
| EP-0827496-A1 | CATALIC ENANTIOSELECTIVE SYNTHESIS OF A SPIRO-FUSED AZETIDINONE | SCHERING CORPORATION (US) | 1998-03-11 | — | — | EP | claimed |
| WO-1996027587-A1 | CATALIC ENANTIOSELECTIVE SYNTHESIS OF A SPIRO-FUSED AZETIDINONE | SCHERING CORPORATION (US) | 1996-09-12 | — | — | WO | claimed |
| CN-120624013-A | Preparation method and application of carbon point X-ray scintillator | 郑州大学 | 2025-09-12 | — | — | CN | disclosed |
| CN-114752372-B | Variable-excitation leadless bimetallic halide monocrystal luminescent material and preparation method and application thereof | 青岛科技大学 | 2025-03-04 | — | — | CN | disclosed |
| CN-119504851-A | Method for preparing phosphine-based compound by catalyzing organic iodine compound | 浙江扬帆新材料股份有限公司 | 2025-02-25 | — | — | CN | disclosed |
| CN-117758369-A | Zero-dimensional silver-based organic-inorganic hybrid metal halide single crystal material, and preparation method and application thereof | 重庆邮电大学 | 2024-03-26 | — | — | CN | disclosed |
| CN-117758369-A | Zero-dimensional silver-based organic-inorganic hybrid metal halide single crystal material, and preparation method and application thereof | 重庆邮电大学 | 2024-03-26 | — | — | CN | disclosed |
| CN-113735901-A | Preparation method of tetraphenyl phosphorus iodide | 西安思科赛实业有限公司 | 2021-12-03 | — | — | CN | disclosed |
| CN-113735901-A | Preparation method of tetraphenyl phosphorus iodide | 西安思科赛实业有限公司 | 2021-12-03 | — | — | CN | disclosed |
| CN-113735901-A | Preparation method of tetraphenyl phosphorus iodide | 西安思科赛实业有限公司 | 2021-12-03 | — | — | CN | disclosed |
| CN-113307827-A | Aqueous phase synthesis method of tetraphenylphosphine phenolate | 山东师范大学实验厂 | 2021-08-27 | — | — | CN | disclosed |
| EP-0827496-A1 | CATALIC ENANTIOSELECTIVE SYNTHESIS OF A SPIRO-FUSED AZETIDINONE | SCHERING CORPORATION (US) | 1998-03-11 | — | — | EP | disclosed |
| WO-1996027587-A1 | CATALIC ENANTIOSELECTIVE SYNTHESIS OF A SPIRO-FUSED AZETIDINONE | SCHERING CORPORATION (US) | 1996-09-12 | — | — | WO | disclosed |