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 SCHEMBL10565259 | 0.97 | — | — | |
| SCHEMBL2201542 | 0.96 | — | — | |
| SCHEMBL58 | 0.96 | — | — | |
| SCHEMBL10376304 | 0.96 | — | — | |
| SCHEMBL4011609 | 0.96 | BRD4 (0.30) | — | |
| SCHEMBL30280996 | 0.93 | — | — | |
| SCHEMBL4511932 | 0.93 | — | — | |
| SCHEMBL28948472 | 0.93 | — | — | |
| Ammonia Solution, Strong SCHEMBL28443159 | 0.93 | — | — | |
| Fluoride SCHEMBL7176780 | 0.93 | — | — |
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 13 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113923988-B | Substituted arylmethyl ureas and heteroarylmethyl ureas, analogs thereof, and methods of using the same | 爱彼特生物制药公司 | 2024-12-13 | — | — | CN | disclosed |
| CN-119059889-A | Haloalkylalkoxymethyl ether compound, process for producing 4,6,8,10,16-pentamethylbehene therefrom, and process for producing synthetic intermediate thereof | 信越化学工业株式会社 | 2024-12-03 | — | — | CN | disclosed |
| CN-119059888-A | Haloalkyl oxymethyl ether compounds, process for preparing 13, 15-dimethylheptadecane therefrom and process for preparing synthetic intermediates thereof | 信越化学工业株式会社 | 2024-12-03 | — | — | CN | disclosed |
| CN-110540761-A | Carbazole-phenothiazine organic dye and application thereof in dye-sensitized solar cell | UNIV NANJING POSTS & TELECOMMUNICATIONS | 2019-12-06 | — | — | CN | disclosed |
| US-20180371144-A1 | LOW TEMPERATURE RADICAL INITIATOR SYSTEM AND PROCESSES MAKING USE THEREOF | STUDIENGESELLSCHAFT KOHLE MBH (DE) | 2018-12-27 | — | — | US | disclosed |
| EP-3394029-A1 | LOW TEMPERATURE RADICAL INITIATOR SYSTEM AND PROCESSES MAKING USE THEREOF | Studiengesellschaft Kohle mbH (DE) | 2018-10-31 | — | — | EP | disclosed |
| WO-2017108761-A1 | LOW TEMPERATURE RADICAL INITIATOR SYSTEM AND PROCESSES MAKING USE THEREOF | STUDIENGESELLSCHAFT KOHLE MBH (DE) | 2017-06-29 | — | — | WO | disclosed |
| EP-3184508-A1 | LOW TEMPERATURE RADICAL INITIATOR SYSTEM AND PROCESSES MAKING USE THEREOF | Studiengesellschaft Kohle MbH (DE) | 2017-06-28 | — | — | EP | disclosed |
| CN-106008488-A | Cyan indoles derivative and preparation method and use thereof | 广东东阳光药业有限公司 | 2016-10-12 | — | — | CN | disclosed |
| CN-101384346-B | Catalytic process for the phosphonylation of high temperature polymers | BASF SE | 2012-05-30 | — | — | CN | disclosed |
| EP-1719773-B1 | FUSED HETEROTETRACYCLIC COMPOUNDS AND USE TEHREOF AS HCV POLYMERASE INHIBITOR | JAPAN TOBACCO INC (JP) | 2009-04-15 | — | — | EP | disclosed |
| CN-101384346-A | Catalytic process for the phosphonylation of high temperature polymers | BASF SE (DE) | 2009-03-11 | — | — | CN | disclosed |
| US-4036631-A | Pyrazolone derivatives and their use as herbicides | SANKYO COMPANY LIMITED (JA) | 1977-07-19 | — | — | US | disclosed |