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 | |
|---|---|---|---|---|
| SCHEMBL385016 | 0.94 | — | — | |
| Water SCHEMBL8463487 | 0.89 | — | — | |
| Bromide SCHEMBL11071949 | 0.89 | — | — | |
| SCHEMBL6889669 | 0.77 | — | — | |
| Iodide SCHEMBL1059358 | 0.74 | — | — | |
| SCHEMBL372326 | 0.67 | — | — | |
| Iodide SCHEMBL394054 | 0.67 | — | — | |
| SCHEMBL2214957 | 0.63 | — | — | |
| SCHEMBL78022 | 0.63 | — | — | |
| Bromide SCHEMBL11615889 | 0.63 | — | — |
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 11 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-6319649-B1 | CAN FORM PATTERN WITH HIGH SENSITIVITY, RESOLUTION ABILITY AND STABILITY, ACCURACY | HITACHI, LTD. (JP) | 2001-11-20 | — | — | US | claimed |
| US-4312818-A | CATALYZED REACTION OF A PHENOL WITH A PHOSPHORUS HALIDE | CIBA-GEIGY CORPORATION (US) | 1982-01-26 | — | — | US | claimed |
| US-20040222401-A1 | Electrochemically stable onium salts and electrolytes containing such for electrochemical capacitors | XU KANG (US) | 2004-11-11 | — | — | US | disclosed |
| US-6743947-B1 | HAVING ASYMMETRIC SUBSTITUTION ON CATION; ALTERING MELTING POINT AND SOLUBILITY | THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE ARMY | 2004-06-01 | — | — | US | disclosed |
| US-6319649-B1 | CAN FORM PATTERN WITH HIGH SENSITIVITY, RESOLUTION ABILITY AND STABILITY, ACCURACY | HITACHI, LTD. (JP) | 2001-11-20 | — | — | US | disclosed |
| EP-0073379-B1 | COMPLEX SALTS WITH INCREASED ELECTRICAL CONDUCTIVITY | BAYER AG (DE) | 1986-08-13 | — | — | EP | disclosed |
| US-4492661-A | Process for producing triarylphosphites | CIBA-GEIGY CORPORATION (US) | 1985-01-08 | — | — | US | disclosed |
| US-4478751-A | Complex salts having high electric conductivity | BAYER AKTIENGESELLSCHAFT (DE) | 1984-10-23 | — | — | US | disclosed |
| US-4440696-A | FROM A PHENOL AND PHOSPHORUS TRIHALIDE, AMINE OR AMIDE CATALYST | CIBA-GEIGY CORPORATION (US) | 1984-04-03 | — | — | US | disclosed |
| EP-0073379-A1 | Complex salts with increased electrical conductivity | BAYER AG (DE) | 1983-03-09 | — | — | EP | disclosed |
| US-4312818-A | CATALYZED REACTION OF A PHENOL WITH A PHOSPHORUS HALIDE | CIBA-GEIGY CORPORATION (US) | 1982-01-26 | — | — | US | disclosed |