Cl- (BioCAD00000008643)
blood cerebrospinal fluid (csf) saliva sweat urine all tissues
Metabolite Card
Formula: Cl (34.9689)
SMILES: [Cl-]
Synonyms [en]
chloride ion; Chloride; Chlorine anion; CL(-); Cl-; Chloride(1-)
Last reviewed on 2024-06-28.
Cite this Page
Cl-. 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: BioCAD00000008643). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
Under standard conditions, chlorine exists as a diatomic molecule. Chlorine is a highly toxic, pale yellow-green gas that has a specific strong smell. In nature, chlorine is most abundant as a chloride ion. Physiologically, it exists as an ion in the body. The chloride ion is an essential anion that the body needs for many critical functions. It also helps keep the body's acid-base balance. The amount of chloride in the blood is carefully controlled by the kidneys. Chloride ions have important physiological roles. For instance, in the central nervous system, the inhibitory action of glycine and some of the action of GABA relies on the entry of Cl- into specific neurons. Also, the chloride-bicarbonate exchanger biological transport protein relies on the chloride ion to increase the blood's capacity of carbon dioxide, in the form of the bicarbonate ion. Chloride-transporting proteins (CLC) play fundamental roles in many tissues in the plasma membrane as well as in intracellular membranes. CLC proteins form a gene family that comprises nine members in mammals, at least four of which are involved in human genetic diseases. GABA(A) receptors are pentameric complexes that function as ligand-gated chloride ion channels. WNK kinases are a family of serine-threonine kinases that have been shown to play an essential role in the regulation of electrolyte homeostasis, and they are found in diverse epithelia throughout the body that are involved in chloride ion flux. Cystic fibrosis (CF) is caused by alterations in the CF transmembrane conductance regulator (CFTCR) gene that result in deranged sodium and chloride ion transport channels. (PMID: 17539703, 17729441, 17562499, 15300163) (For a complete review see Evans, Richard B. Chlorine: state of the art. Lung (2005), 183(3), 151-167. PMID: 16078037).
DBLinks
- CAS Registry Number: 16887-00-6
- PubChem CID: 312
- ChEBI: 17996
- HMDB: HMDB0000492
- LipidMaps:
- KEGG: C00698
- BioCyc: CL-
- NCBI MeSH: Chlorides
- Wikipedia: Chloride
Other DBLinks
- CAS Registry Number: 131500-00-0
- CAS Registry Number: 139512-37-1
- CAS Registry Number: 155522-09-1
- CAS Registry Number: 16887-00-6
- PubChem: 312
- ChEBI: ChEBI:17996
- HMDB: HMDB0000492
- KEGG: C00698
- BioCyc: CL-
- NCBI MeSH: Chlorides
- Wikipedia: Chloride
- DrugBank: DB14547
Class / Ontology
- WishartLab ClassyFire: [Homogeneous halogens] Homogeneous halogens
- ChEBI: [CHEBI:17996] chloride
| ID | EC Number | Name |
|---|---|---|
| KEGG:R01032 | 3-chloro-L-alanine chloride-lyase (deaminating; pyruvate-forming) | |
| KEGG:R01033 | 1.14.12.13 | 2-chlorobenzoate,NADH:oxygen oxidoreductase (1,2-hydroxylating, dechlorinating, decarboxylating) |
| KEGG:R01307 | 3.8.1.6 | 4-chlorobenzoate chlorohydrolase |
| KEGG:R02605 | 4.5.1.4 | L-2-amino-4-chloropent-4-enoate chloride-lyase (deaminating) |
| KEGG:R03523 | 3.8.1.5 | bromochloromethane halidohydrolase |
| KEGG:R03982 | 1.14.13.50 | pentachlorophenol,NADPH:oxygen oxidoreductase (hydroxylating, dechloronating) |
| KEGG:R04003 | 4.5.1.5 | 3-chloro-L-alanine chloride-lyase (adding thioglycolate) |
| KEGG:R04101 | 3.8.1.7 | 4-chlorobenzoyl CoA chlorohydrolase |
| KEGG:R05268 | C04596 + C00080<=>C06637 + C00698 | |
| KEGG:R05355 | 1.3.1.32 | C06329 + C00004<=>C02222 + C00003 + C00698 |
| KEGG:R05446 | 1.14.14.- | C06600 + C01352 + C00007<=>C21105 + C00016 + C00001 + C00698 |
| KEGG:R05447 | 1.14.14.- | C07101 + C01352 + C00007<=>C21104 + C00016 + C00001 + C00698 |
| KEGG:R05449 | 1.14.14.173 | 2,4,6-trichlorophenol,FADH2:oxygen oxidoreductase (dechlorinating) |
| KEGG:R05476 | C04623<=>C06636 + C00698 | |
| KEGG:R05497 | 1.97.1.- | C04596<=>C06637 + C00698 |
| KEGG:R05504 | 1.97.1.- | C07089 + C00080<=>C00682 + C00698 |
| KEGG:R05505 | 1.97.1.- | C03664 + C00080 + 2 C05359<=>C07088 + C00698 |
| KEGG:R05533 | C06988<=>C06989 + 2 C00698 | |
| KEGG:R05534 | C06989<=>C11352 + 2 C00698 | |
| KEGG:R05535 | C11352<=>C06990 + C00698 + C00080 |
Taxonomy Source
Pathway Synthetic
| pathway id | name |
|---|---|
| BioCyc:HUMAN_TRYPTOPHAN-DEGRADATION-1 | tryptophan degradation |
| BioCyc:HUMAN_PWY66-401 | superpathway of tryptophan utilization |
| BioCyc:META_PWY-7428 | 2-chloroacrylate degradation II |
| BioCyc:META_14DICHLORBENZDEG-PWY | 1,4-dichlorobenzene degradation |
| BioCyc:META_PWY-6628 | superpathway of L-phenylalanine biosynthesis |
| BioCyc:META_CYANCAT-PWY | cyanate degradation |
| BioCyc:META_PWY-7229 | superpathway of adenosine nucleotides de novo biosynthesis I |
| BioCyc:META_GLUCARDEG-PWY | D-glucarate degradation I |
| BioCyc:META_PWY-6954 | superpathway of aromatic compound degradation via 2-hydroxypentadienoate |
| BioCyc:META_PWY-7008 | 2-hydroxybiphenyl degradation |
| BioCyc:META_1CMET2-PWY | N10-formyl-tetrahydrofolate biosynthesis |
| BioCyc:META_PWY-2201 | folate transformations I |
| BioCyc:META_PWY-7930 | pyoluteorin biosynthesis |
| BioCyc:META_SER-GLYSYN-PWY | superpathway of L-serine and glycine biosynthesis I |
| BioCyc:META_ALL-CHORISMATE-PWY | superpathway of chorismate metabolism |
| BioCyc:META_PWY-6192 | 3,4-dichlorotoluene degradation |
| BioCyc:META_PWY-6190 | 2,4-dichlorotoluene degradation |
| BioCyc:META_PWY-5724 | superpathway of atrazine degradation |
| BioCyc:META_PWY-6193 | 3-chlorocatechol degradation II (ortho) |
| BioCyc:META_PWY-6214 | 3-chlorocatechol degradation III (meta pathway) |