Known targets — ChEMBL curated mechanism
ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4
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.
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 | |
|---|---|---|---|---|
| Bromide SCHEMBL1856 | 1.00 | — | — | |
| Bromide SCHEMBL11224381 | 1.00 | — | — | |
| Bromide SCHEMBL82194 | 1.00 | — | — | |
| Bromide SCHEMBL312889 | 1.00 | — | — | |
| Bromide SCHEMBL6294269 | 1.00 | — | — | |
| Bromide SCHEMBL10784827 | 0.82 | — | — | |
| Bromide SCHEMBL3326847 | 0.82 | — | — | |
| Bromide SCHEMBL11116971 | 0.82 | — | — | |
| Bromide SCHEMBL11404944 | 0.82 | — | — | |
| Bromide SCHEMBL11418208 | 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 11 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| JP-6080647-A | — | — | None | — | — | JP | disclosed |
| WO-2020235968-A1 | ELECTROLYTE ADDITIVE FOR SECONDARY BATTERY, PREPARATION METHOD THEREFOR, AND ELECTROLYTE COMPOSITION AND SECONDARY BATTERY, WHICH COMPRISE ADDITIVE | (주)후성 (KR) | 2020-11-26 | — | — | WO | disclosed |
| US-7189873-B2 | Propargylether derivatives, a process for their preparation and their use for controlling phytopathogenic microorganisms | SYNGENTA CORP PROTECTION, INC. (US) | 2007-03-13 | — | — | US | disclosed |
| EP-1549609-B1 | PROPARGYLETHER DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND THEIR USE FOR CONTROLLING PHYTOPATHOGENIC MICROORGANISMS | SYNGENTA PARTICIPATIONS AG (CH) | 2007-01-24 | — | — | EP | disclosed |
| US-20060167316-A1 | Propargylether derivatives, a process for their preparation and their use for controlling phytopathogenic microorganisms | SYNGENTA CROP PROTECTION, INC. | 2006-07-27 | — | — | US | disclosed |
| EP-1549609-A2 | PROPARGYLETHER DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND THEIR USE FOR CONTROLLING PHYTOPATHOGENIC MICROORGANISMS | Syngenta Participations AG (CH) | 2005-07-06 | — | — | EP | disclosed |
| WO-2004033413-A2 | PROPARGYLETHER DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND THEIR USE FOR CONTROLLING PHYTOPATHOGENIC MICROORGANISMS | SYNGENTA PARTICIPATIONS AG (CH) | 2004-04-22 | — | — | WO | disclosed |
| EP-0724586-B1 | PROCESS FOR PREPARING N-(2,6-DICHLORO-3-METHYLPHENYL)-5-7-DIHALO[1,2,4]TRIAZOLO[1,5A]PYRIMIDINE-2-SULFONAMIDE BY CYCLIZATION AND HALO-DEHYDROXYLATION | DOW AGROSCIENCES LLC (US) | 2002-01-23 | — | — | EP | disclosed |
| US-6248919-B1 | E.G., (2S)-2-(((5-((BUTYL(2-CYCLOHEXYLETHYL)AMINO)METHYL) -2'-METHYL(1,1'-BIPHENYL)-2-YL)CARBONYL)AMINO)-4-(METHYLSULFAN YL)BUTANOIC ACID, OR A PHARMACEUTICALLY ACCEPTABLE SALT OR PRODRUG THEREOF. | ABBOTT LABORATORIES | 2001-06-19 | — | — | US | disclosed |
| US-5703258-A | FLAME RETARDERS | BLOUNT DAVID H (US) | 1997-12-30 | — | — | US | disclosed |
| JP-H0680647-A | NEW QUINAZOLINE DERIVATIVE | HISAMITSU PHARMACEUT CO INC | 1994-03-22 | — | — | JP | disclosed |