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 2)
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 | |
|---|---|---|---|---|
| Water SCHEMBL1067074 | 0.91 | DNM1 (0.44) | DNM1TSHR | |
| Bromide SCHEMBL808510 | 0.91 | DNM1 (0.50) | DNM1TSHR | |
| Bromide SCHEMBL302452 | 0.91 | DNM1 (0.50) | DNM1TSHR | |
| Fluoride Ion SCHEMBL942194 | 0.91 | DNM1 (0.44) | DNM1TSHR | |
| SCHEMBL10386415 | 0.91 | DNM1 (0.44) | DNM1TSHR | |
| Hydrochloric Acid SCHEMBL933212 | 0.91 | DNM1 (0.44) | DNM1TSHR | |
| SCHEMBL2858147 | 0.87 | DNM1 (0.42) | DNM1TSHR | |
| Iodide SCHEMBL5087539 | 0.86 | DNM1 (0.67) | DNM1TSHR | |
| Iodide SCHEMBL5088401 | 0.86 | DNM1 (0.67) | DNM1TSHR | |
| Iodide SCHEMBL5087491 | 0.86 | DNM1 (0.67) | DNM1TSHR |
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 43 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0520130-B1 | Process for preparing symmetric N, N'-disubstituted aromatic urea | LUCKY LTD (KR) | 1995-04-12 | — | — | EP | claimed |
| US-5198582-A | Process for preparing symmetric N,N'-disubstituted aromatic urea | LUCKY LTD. (KR) | 1993-03-30 | — | — | US | claimed |
| US-20080214386-A1 | Stability; easily separated from solution; surface treatment of catalyst with Group seven compound; reacting epoxide with carbon dioxide | NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) | 2008-09-04 | — | — | US | disclosed |
| EP-0502707-B1 | Method for production of 3-cyano-3,5,5-trimethyl cyclohexanone | NIPPOH CHEMICALS (JP) | 1995-10-25 | — | — | EP | disclosed |
| EP-0520130-B1 | Process for preparing symmetric N, N'-disubstituted aromatic urea | LUCKY LTD (KR) | 1995-04-12 | — | — | EP | disclosed |
| US-5198582-A | Process for preparing symmetric N,N'-disubstituted aromatic urea | LUCKY LTD. (KR) | 1993-03-30 | — | — | US | disclosed |
| EP-0283586-B1 | HOMOLOGATION PROCESS | UNION CARBIDE CORPORATION (US) | 1993-03-17 | — | — | EP | disclosed |
| US-5179221-A | METHOD FOR PRODUCTION OF 3-CYANO-3,5,5-TRIMETHYL CYCLOHEXANONE | NIPPON CHEMICALS CO., LTD. (JP) | 1993-01-12 | — | — | US | disclosed |
| EP-0520130-A1 | Process for preparing symmetric N, N'-disubstituted aromatic urea | LUCKY LTD. (KR) | 1992-12-30 | — | — | EP | disclosed |
| EP-0502707-A1 | Method for production of 3-cyano-3,5,5-trimethyl cyclohexanone | NIPPOH CHEMICALS CO., LTD. (JP) | 1992-09-09 | — | — | EP | disclosed |
| EP-0340985-B1 | PROCESS FOR PREPARING TRANS-2,2-DIMETHYL-3-(2,2-DIHALOVINYL)-CYCLOPROPANE CARBOXYLIC ACID HALIDE | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1992-07-08 | — | — | EP | disclosed |
| US-4429165-A | TRIVALENT ORGANOPHOSPHORUS AND ORGANONITROGEN COMPOUNDS AS PROMOTERS | UNION CARBIDE CORPORATION (US) | 1984-01-31 | — | — | US | disclosed |
| EP-0034374-B1 | SELECTIVE HOMOLOGATION OF ACETALS OR ETHERS TO MONOHYDRIC OR POLYHYDRIC ALCOHOLS | UNION CARBIDE CORPORATION (US) | 1983-08-03 | — | — | EP | disclosed |
| US-4337365-A | COBALT AND IODIDE CATALYST, HIGH TEMPERATURE, INERT ETHER SOLVENT | UNION CARBIDE CORPORATION (US) | 1982-06-29 | — | — | US | disclosed |
| EP-0037586-A1 | Process for the selective hydroformylation of methanol to acetaldehyde | UNION CARBIDE CORPORATION (US) | 1981-10-14 | — | — | EP | disclosed |
| EP-0037580-A1 | Process for the selective homologation of methanol to ethanol | UNION CARBIDE CORPORATION (US) | 1981-10-14 | — | — | EP | disclosed |
| EP-0034374-A1 | Selective homologation of acetals or ethers to monohydric or polyhydric alcohols | UNION CARBIDE CORPORATION (US) | 1981-08-26 | — | — | EP | disclosed |
| US-4277634-A | SYNERGISTIC COMBINATION OF COBALT CATALYST, IODINE PROMOTER, AND INERT SOLVENT | UNION CARBIDE CORPORATION (US) | 1981-07-07 | — | — | US | disclosed |
| US-4124630-A | Process for the production of chloromethyl thiocyanate | OFFERMANNS HERIBERT | 1978-11-07 | — | — | US | disclosed |
| US-4052427-A | PROCESS FOR THE PREPARATION OF DIALKYLTIN DIHALIDES | WITCO CHEMICAL CORPORATION (US) | 1977-10-04 | — | — | US | disclosed |