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 | |
|---|---|---|---|---|
| Iodide SCHEMBL176899 | 1.00 | — | — | |
| Iodide SCHEMBL3382952 | 1.00 | — | — | |
| Iodide SCHEMBL28299602 | 1.00 | — | — | |
| Iodide SCHEMBL3374494 | 1.00 | CA4 (0.50) | — | |
| Iodide SCHEMBL31472568 | 1.00 | — | — | |
| Iodide SCHEMBL27902781 | 1.00 | — | — | |
| Iodide SCHEMBL28105529 | 1.00 | — | — | |
| Iodide SCHEMBL27569 | 1.00 | — | — | |
| Iodide SCHEMBL69895 | 1.00 | — | — | |
| Iodide SCHEMBL9278729 | 0.82 | — | — |
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 9 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113166594-A | Latent reactive adhesive film | 德莎欧洲股份公司 | 2021-07-23 | — | — | CN | disclosed |
| US-6232312-B1 | ADMINISTERING A COMBINATION OF INDENE AND PYRIMIDO(5,4-D)PYRIMIDINE DERIVATIVES TO TREAT PREPANCREATIC CANCER | CELL PATHWAYS, INC. | 2001-05-15 | — | — | US | disclosed |
| US-4556744-A | Process for the production of ethanol and/or acetaldehyde by the metal catalysed liquid phase reaction of methanol, carbon monoxide and hydrogen in the presence of a solvent | THE BRITISH PETROLEUM COMPANY P.L.C. (GB) | 1985-12-03 | — | — | US | disclosed |
| EP-0141535-A2 | Process for the production of ethanol and/or acetaldehyde by the metal catalysed liquid phase reaction of methanol, carbon monoxide and hydrogen in the presence of a solvent | The British Petroleum Company p.l.c. (GB) | 1985-05-15 | — | — | EP | disclosed |
| US-RE30430-E | Catalyst treatment | DENKA CHEMICAL CORPORATION (US) | 1980-11-04 | — | — | US | disclosed |
| US-RE30279-E | FROM ALKYL OR ARYL HALIDE WITH HALO-SUBSTITUTED TRIVALENT PHOSPHORUS COMPOUNDS AND PHOSPHORUS PENTASULFIDE OR -OXIDE | STAUFFER CHEMICAL COMPANY (US) | 1980-05-20 | — | — | US | disclosed |
| US-4081460-A | IN SITU REGENERATION AND STABILIZATION OF CATALYST WITH A PHOSPHORUS COMPOUND | DENKA CHEMICAL CORPORATION (US) | 1978-03-28 | — | — | US | disclosed |
| US-4073809-A | Method for producing trialkylphosphine oxides | KANDUL JURY VASILIEVICH | 1978-02-14 | — | — | US | disclosed |
| US-4006168-A | Catalyst treatment | PETRO-TEX CHEMICAL CORPORATION (US) | 1977-02-01 | — | — | US | disclosed |