Bromide (BioCAD00000007617)
Metabolite Card
Formula: Br (78.9183)
SMILES: [Br-]
Synonyms [en]
Bromide; BROMIDE ion; Bromides; Br(-); bromine anion; Br-
Last reviewed on 2024-06-28.
Cite this Page
Bromide. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000007617). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
Bromine is a brown or red liquid with a characteristic odor. Bromine is mainly used in the manufacture of dyes, inks, flame retardants, pharmaceuticals and chemical warfare agents. Occupational exposure to bromine may occur during the production and the application of bromine compounds and during other industrial activities. This compound is adsorbed into the human body through the respiratory tract, skin (occupational exposure) and alimentary tract (general population). Physiologically, bromine exists as an ion in the body. Slight eye irritation occurs as a consequence of chronic exposure to bromine vapors at concentration of 1 mg/m3. Higher concentrations increase this effect and cause nasal and skin irritation. Many years' observations have shown that during occupational exposure to bromine vapors at concentrations of up to 0.7 mg/m3 (0.1 ppm), there are no observed adverse effects. From cytotoxicity and mutagenicity assays, it is known that brominated organic compounds are more toxic than chlorinated organic compounds. However, only a limited number of brominated organic compounds have been regulated. (PMID: 17316744).
DBLinks
- CAS Registry Number: 24959-67-9
- PubChem CID: 259
- ChEBI: 15858
- HMDB: HMDB0002500
- LipidMaps:
- KEGG: C01324
- BioCyc: BR-
- NCBI MeSH: Bromides
- Wikipedia: Bromide
Other DBLinks
- CAS Registry Number: 24959-67-9
- CAS Registry Number: 7726-95-6
- PubChem: 259
- ChEBI: ChEBI:15858
- HMDB: HMDB0002500
- KEGG: C01324
- BioCyc: BR-
- NCBI MeSH: Bromides
- Wikipedia: Bromide
- Wikipedia: Tetrabenazine
Class / Ontology
- WishartLab ClassyFire: [Homogeneous halogens] Homogeneous halogens
| ID | EC Number | Name |
|---|---|---|
| KEGG:R03523 | 3.8.1.5 | bromochloromethane halidohydrolase |
| KEGG:R07781 | 1.3.1.32 | 2-maleylacetate:NAD+ oxidoreductase |
| KEGG:R12013 | 1.14.19.55 | 4-hydroxybenzoate:NADPH oxidoreductase (brominating, decarboxylating) |
| KEGG:R12015 | 1.14.19.55 | C00156 + C00005 + C01324 + C00007 + 2 C00080<=>C21850 + C00006 + 2 C00001 |
| KEGG:R12016 | 1.14.19.55 | C21850 + C00005 + C01324 + C00007 + 2 C00080<=>C14521 + C00006 + C00011 + 2 C00001 |
| KEGG:R12018 | 1.14.19.55 | 3,4-dihydroxybenzoate:NADPH oxidoreductase (brominating, decarboxylating) |
| KEGG:R12019 | 1.14.19.55 | C00230 + C00005 + C01324 + C00007 + 2 C00080<=>C21853 + C00006 + 2 C00001 |
| KEGG:R12020 | 1.14.19.55 | C21853 + C00005 + C01324 + C00007 + 2 C00080<=>C21852 + C00006 + C00011 + 2 C00001 |
| KEGG:R12027 | 1.14.19.57 | C12483 + C01352 + C01324 + C00007<=>C21862 + C00016 + 2 C00001 |
| KEGG:R12028 | 1.14.19.57 | C21862 + C01352 + C01324 + C00007<=>C21863 + C00016 + 2 C00001 |
| KEGG:R12029 | 1.14.19.57 | C21863 + C01352 + C01324 + C00007<=>C21864 + C00016 + 2 C00001 |
| KEGG:R12030 | 1.14.19.57 | 1H-pyrrole-2-carbonyl-[peptidyl-carrier protein]:FADH2 oxidoreductase (brominating) |
| KEGG:R13631 | 1.14.19.82 | L-tryptophan:NADPH oxidoreductase (5-brominating) |
| BioCyc:RXN0-6549 | BROMOACETATE + GLUTATHIONE --> PROTON + CPD0-2370 + BR- | |
| Rhea:RHEA:13766 | bromochloromethane + H2O => bromide + formaldehyde + chloride + 2 H+ | |
| Rhea:RHEA:13767 | bromide + formaldehyde + chloride + 2 H+ => bromochloromethane + H2O | |
| Rhea:RHEA:13768 | bromochloromethane + H2O <=> bromide + formaldehyde + chloride + 2 H+ | |
| Rhea:RHEA:27366 | 2.1.1.165 | bromide + S-adenosyl-L-methionine => bromomethane + S-adenosyl-L-homocysteine |
| Rhea:RHEA:27367 | 2.1.1.165 | bromomethane + S-adenosyl-L-homocysteine => bromide + S-adenosyl-L-methionine |
| Rhea:RHEA:27368 | 2.1.1.165 | bromide + S-adenosyl-L-methionine <=> bromomethane + S-adenosyl-L-homocysteine |
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| BioCyc:META_CYANCAT-PWY | cyanate degradation |
| BioCyc:META_GLUCARDEG-PWY | D-glucarate degradation I |
| BioCyc:META_PWY-7933 | superpathway of polybrominated aromatic compound biosynthesis |
| BioCyc:ECO_GALACTARDEG-PWY | D-galactarate degradation I |
| BioCyc:ECO_CYANCAT-PWY | cyanate degradation |
| BioCyc:ARA_PWY-6730 | methylhalides biosynthesis (plants) |
| BioCyc:META_ASPARAGINE-DEG1-PWY | L-asparagine degradation I |
| BioCyc:META_PWY1G-1 | mycothiol-mediated detoxification |
| BioCyc:META_PWY-6730 | methylhalides biosynthesis (plants) |
| BioCyc:META_PWY-7931 | brominated pyrroles biosynthesis |
| BioCyc:META_PWY-7935 | spongiadioxin C biosynthesis |
| BioCyc:ECO_GLUCARDEG-PWY | D-glucarate degradation I |
| BioCyc:ECO_GLUCARGALACTSUPER-PWY | superpathway of D-glucarate and D-galactarate degradation |
| BioCyc:META_PWY-6516 | superpathway of microbial D-galacturonate and D-glucuronate degradation |
| BioCyc:META_PWY-7932 | polybrominated biphenyls and diphenyl ethers biosynthesis |
| BioCyc:META_PWY-7929 | polybrominated phenols biosynthesis |
| BioCyc:META_PWY-7934 | polybrominated dihydroxylated diphenyl ethers biosynthesis |
| BioCyc:META_PWY-5634 | superpathway of penicillin, cephalosporin and cephamycin biosynthesis |
| BioCyc:META_PWY-5631 | deacetylcephalosporin C biosynthesis |
| BioCyc:META_PWY-723 | alkylnitronates degradation |