Known targets — ChEMBL curated mechanism
ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1
The experimentally established mechanism targets of Bromide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SLC22A1 | O15245 | 3/20 | 0.69 |
| ▸ | DNM1 | Q05193 | 5/20 | 0.68 |
| ▸ | TSHR | P16473 | 2/20 | 0.61 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.61 |
| ▸ | TP53 | P04637 | 1/20 | 0.61 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.61 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.61 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.61 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.61 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.61 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.61 |
| ▸ | SLC22A2 | O15244 | 1/20 | 0.59 |
| ▸ | NFKB1 | P19838 | 1/20 | 0.44 |
| ▸ | KCNA1 | Q09470 | 1/20 | 0.44 |
| ▸ | HSP90AA1 | P07900 | 1/20 | 0.43 |
| ▸ | RAD52 | P43351 | 1/20 | 0.43 |
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 | |
|---|---|---|---|---|
| SCHEMBL28793843 | 0.97 | SLC22A1 (0.73) | SLC22A1DNM1TSHRALDH1A1TP53 | |
| SCHEMBL3876642 | 0.97 | SLC22A1 (0.73) | SLC22A1DNM1TSHRALDH1A1TP53 | |
| Bromide SCHEMBL622840 | 0.93 | DNM1 (0.78) | SLC22A1DNM1TSHRALDH1A1TP53 | |
| SCHEMBL7638959 | 0.93 | SLC22A1 (0.69) | SLC22A1DNM1TSHRALDH1A1TP53 | |
| Water SCHEMBL3304283 | 0.93 | SLC22A1 (0.69) | SLC22A1DNM1TSHRALDH1A1TP53 | |
| SCHEMBL7553616 | 0.93 | SLC22A1 (0.69) | SLC22A1DNM1TSHRALDH1A1TP53 | |
| Bromide SCHEMBL3680180 | 0.93 | SLC22A1 (0.69) | SLC22A1DNM1TSHRALDH1A1TP53 | |
| SCHEMBL7553619 | 0.93 | SLC22A1 (0.69) | SLC22A1DNM1TSHRALDH1A1TP53 | |
| Iodide SCHEMBL5086874 | 0.93 | SLC22A1 (0.69) | SLC22A1DNM1TSHRALDH1A1TP53 | |
| SCHEMBL27846084 | 0.93 | SLC22A1 (0.69) | SLC22A1DNM1TSHRALDH1A1TP53 |
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 15 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-101396690-B | Multilayer coating film-forming method | KANSAI PAINT CO LTD | 2013-08-21 | — | — | CN | claimed |
| US-4522729-A | CXONTACTING IMPORITIES WITH TETRAALKYLAMMONIUM SALT | PHILLIPS PETROLEUM COMPANY (US) | 1985-06-11 | — | — | US | claimed |
| WO-2024190910-A1 | ONE-COMPONENT CURABLE COATING COMPOSITION | 関西ペイント株式会社 | 2024-09-19 | — | — | WO | disclosed |
| CN-101396690-B | Multilayer coating film-forming method | KANSAI PAINT CO LTD | 2013-08-21 | — | — | CN | disclosed |
| CN-101293238-B | Multilayer coating film- forming method | KANSAI PAINT CO LTD | 2013-05-01 | — | — | CN | disclosed |
| US-8048491-B2 | 2-coat-1-bake system; an acrylic-type acid and/or acrylic-type anhydride, an epoxy-functional acrylic resin, and a glycol ether solvent; improved workability, electrostatic coatability, and gloss; clear coat paints | KANSAI PAINT CO., LTD. (JP) | 2011-11-01 | — | — | US | disclosed |
| US-20090087667-A1 | Multilayer coating film-forming method | KANSAI PAINT CO., LTD. | 2009-04-02 | — | — | US | disclosed |
| CN-101396690-A | Multilayer coating film-forming method | KANSAI PAINT CO LTD (JP) | 2009-04-01 | — | — | CN | disclosed |
| US-20080268256-A1 | Multilayer coating film- forming method | KANSAI PAINT CO., LTD. | 2008-10-30 | — | — | US | disclosed |
| CN-101293238-A | Multilayer coating film- forming method | KANSAI PAINT CO LTD (JP) | 2008-10-29 | — | — | CN | disclosed |
| 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-0161550-B1 | PROCESS FOR PRODUCING AN ALIPHATIC ISOCYANATE | Asahi Kasei Kogyo Kabushiki Kaisha (JP) | 1988-01-20 | — | — | EP | disclosed |
| US-4587056-A | CARBONYLATION, OXIDATION, CATALYST | ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) | 1986-05-06 | — | — | US | disclosed |
| EP-0161550-A1 | Process for producing an aliphatic isocyanate | Asahi Kasei Kogyo Kabushiki Kaisha (JP) | 1985-11-21 | — | — | EP | disclosed |
| US-4522729-A | CXONTACTING IMPORITIES WITH TETRAALKYLAMMONIUM SALT | PHILLIPS PETROLEUM COMPANY (US) | 1985-06-11 | — | — | US | disclosed |