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 | |
|---|---|---|---|---|
| ▸ | ACHE known ✓ | P22303 | 6/20 | 0.53 |
| ▸ | ALDH1A1 | P00352 | 6/20 | 0.58 |
| ▸ | TSHR | P16473 | 4/20 | 0.58 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.53 |
| ▸ | CA2 | P00918 | 2/20 | 0.41 |
| ▸ | LPL | P06858 | 1/20 | 0.41 |
| ▸ | LIPG | Q9Y5X9 | 1/20 | 0.41 |
| ▸ | MAPT | P10636 | 2/20 | 0.41 |
| ▸ | CYP2C19 | P33261 | 2/20 | 0.41 |
| ▸ | MCOLN3 | Q8TDD5 | 1/20 | 0.41 |
| ▸ | CA1 | P00915 | 1/20 | 0.40 |
| ▸ | CA7 | P43166 | 1/20 | 0.40 |
| ▸ | CA9 | Q16790 | 1/20 | 0.40 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.38 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.38 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.38 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.38 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.38 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.38 |
| ▸ | CHRNA7 | P36544 | 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 | |
|---|---|---|---|---|
| SCHEMBL16982395 | 0.97 | ALDH1A1 (0.61) | ALDH1A1TSHRACHETDP1CA2 | |
| SCHEMBL6123161 | 0.97 | ALDH1A1 (0.61) | ALDH1A1TSHRACHETDP1CA2 | |
| SCHEMBL4893877 | 0.97 | ALDH1A1 (0.61) | ALDH1A1TSHRACHETDP1CA2 | |
| SCHEMBL7486403 | 0.97 | ALDH1A1 (0.61) | ALDH1A1TSHRACHETDP1CA2 | |
| SCHEMBL76680 | 0.97 | ALDH1A1 (0.61) | ALDH1A1TSHRACHETDP1CA2 | |
| SCHEMBL12240222 | 0.97 | ALDH1A1 (0.61) | ALDH1A1TSHRACHETDP1CA2 | |
| SCHEMBL615437 | 0.97 | ALDH1A1 (0.61) | ALDH1A1TSHRACHETDP1CA2 | |
| Hydrochloric Acid SCHEMBL25295730 | 0.93 | ALDH1A1 (0.58) | ALDH1A1TSHRACHETDP1CA2 | |
| Ammonia Solution, Strong SCHEMBL8759606 | 0.93 | ALDH1A1 (0.58) | ALDH1A1TSHRACHETDP1CA2 | |
| Hydrochloric Acid SCHEMBL8469549 | 0.90 | ALDH1A1 (0.55) | ALDH1A1TSHRACHETDP1CA2 |
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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119505867-A | Gold nanocluster and application thereof in organophosphorus pesticide residue detection | 河南省农业科学院农产品质量安全研究所 | 2025-02-25 | — | — | CN | disclosed |
| EP-0283586-B1 | HOMOLOGATION PROCESS | UNION CARBIDE CORPORATION (US) | 1993-03-17 | — | — | EP | disclosed |
| US-5026907-A | High efficiency, selectivity with lithium, sodium or potassium iodide combined with phophorous ligand of complex; reacting alcohol, ester and carbon monoxide | UNION CARBIDE CHEMICALS AND PLASTICS TECHNOLOGY CORPORATION (US) | 1991-06-25 | — | — | US | disclosed |
| US-4990654-A | Reacting mixture of methanol and ethanol with carbon monoxide using halogen-promoted phosphorus-containing catalyst system | UNION CARBIDE CHEMICALS AND PLASTICS COMPANY INC. (US) | 1991-02-05 | — | — | US | disclosed |
| US-4927967-A | Production of carboxylic acids from organic formate esters using rhodium complex catalysts | UNION CARBIDE CHEMICALS AND PLASTICS COMPANY INC. (US) | 1990-05-22 | — | — | US | disclosed |
| EP-0173170-B1 | PROCESS FOR THE PREPARATION OF ANHYDROUS CARBOXYLIC ACIDS FROM ALCOHOLS | UNION CARBIDE CORPORATION (US) | 1989-09-20 | — | — | EP | disclosed |
| EP-0283586-A2 | Homologation process | UNION CARBIDE CORPORATION (US) | 1988-09-28 | — | — | EP | disclosed |
| EP-0171802-B1 | PRODUCTION OF CARBOXYLIC ANHYDRIDES FROM METHYL CARBOXYLATES USING RHODIUM COMPLEX CATALYSTS | UNION CARBIDE CORPORATION (US) | 1988-04-06 | — | — | EP | disclosed |
| US-4727200-A | RHODIUM-BASED CATALYST; MILD CONDITIONS | UNION CARBIDE CORPORATION (US) | 1988-02-23 | — | — | US | disclosed |
| EP-0171652-B1 | PRODUCTION OF CARBOXYLIC ACIDS FROM ALCOHOLS USING RHODIUM COMPLEX CATALYSTS | UNION CARBIDE CORPORATION (US) | 1988-01-27 | — | — | EP | disclosed |
| EP-0171652-A1 | Production of carboxylic acids from alcohols using rhodium complex catalysts | UNION CARBIDE CORPORATION (US) | 1986-02-19 | — | — | EP | disclosed |
| EP-0171804-A2 | Production of acetate esters from alcohols using rhodium complex catalysts | UNION CARBIDE CORPORATION (US) | 1986-02-19 | — | — | EP | disclosed |
| EP-0171651-A1 | Production of carboxylic acids from organic formates using rhodium complex catalysts | UNION CARBIDE CORPORATION (US) | 1986-02-19 | — | — | EP | disclosed |
| EP-0171802-A1 | Production of carboxylic anhydrides from methyl carboxylates using rhodium complex catalysts | UNION CARBIDE CORPORATION (US) | 1986-02-19 | — | — | EP | disclosed |
| WO-1986000889-A1 | PRODUCTION OF CARBOXYLIC ACIDS FROM ORGANIC FORMATE ESTERS USING RHODIUM COMPLEX CATALYSTS | UNION CARBIDE CORPORATION (US) | 1986-02-13 | — | — | WO | disclosed |
| WO-1986000888-A1 | PRODUCTION OF CARBOXYLIC ACIDS FROM ALCOHOLS USING RHODIUM COMPLEX CATALYSTS | UNION CARBIDE CORPORATION (US) | 1986-02-13 | — | — | WO | disclosed |
| US-4563309-A | CARBONYLATION | UNION CARBIDE CORPORATION (US) | 1986-01-07 | — | — | US | disclosed |
| US-4490559-A | SYNTHESIS GAS AND A GROUP VII COMPOUND CATALYST | SHELL OIL COMPANY (US) | 1984-12-25 | — | — | US | disclosed |
| US-4447648-A | USING SYNTHESIS GAS AND A GROUP VIII COMPOUND | UNION CARBIDE CORPORATION (US) | 1984-05-08 | — | — | US | disclosed |
| US-4429165-A | TRIVALENT ORGANOPHOSPHORUS AND ORGANONITROGEN COMPOUNDS AS PROMOTERS | UNION CARBIDE CORPORATION (US) | 1984-01-31 | — | — | US | disclosed |