Bromide (BioCAD00000007617)

blood cerebrospinal fluid (csf) urine kidney liver

Metabolite Card

Formula: Br (78.9183)
SMILES: [Br-]

Synonyms [en]

Bromide; BROMIDE ion; Bromides; Br(-); bromine anion; Br-

Reviewed

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).

Entity Information

DBLinks

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

Metabolic Network
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
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Organism Source

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
View All Pathways