CHEBI:17300 - tetrachloroethene

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ChEBI Name tetrachloroethene
ChEBI ID CHEBI:17300
Definition A chlorocarbon that is tetrachloro substituted ethene.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:15216, CHEBI:9471, CHEBI:26890
Supplier Information ZINC000008214733
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Adenosine triphosphate (ATP) is a nucleoside triphosphate that provides energy to drive and support many processes in living cells, such as muscle contraction, nerve impulse propagation, and chemical synthesis. Found in all known forms of life, it is often referred to as the "molecular unit of currency" for intracellular energy transfer. When consumed in a metabolic process, ATP converts either to adenosine diphosphate (ADP) or to adenosine monophosphate (AMP). Other processes regenerate ATP. It is also a precursor to DNA and RNA, and is used as a coenzyme. An average adult human processes around 50 kilograms (about 100 moles) daily. From the perspective of biochemistry, ATP is classified as a nucleoside triphosphate, which indicates that it consists of three components: a nitrogenous base (adenine), the sugar ribose, and the triphosphate.
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Formula C2Cl4
Net Charge 0
Average Mass 165.83220
Monoisotopic Mass 163.87541
InChI InChI=1S/C2Cl4/c3-1(4)2(5)6
InChIKey CYTYCFOTNPOANT-UHFFFAOYSA-N
SMILES ClC(Cl)=C(Cl)Cl
Roles Classification
Biological Role(s): nephrotoxic agent
A role played by any chemical compound (natural or synthetic) exhibiting itself through the ability to induce damage to the kidneys.
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ChEBI Ontology
Outgoing tetrachloroethene (CHEBI:17300) has role nephrotoxic agent (CHEBI:50909)
tetrachloroethene (CHEBI:17300) is a chlorocarbon (CHEBI:39226)
tetrachloroethene (CHEBI:17300) is a chloroethenes (CHEBI:23142)
IUPAC Name
tetrachloroethene
Synonyms Sources
1,1,2,2-tetrachloroethylene UM-BBD
ethylene tetrachloride ChemIDplus
PCE KEGG COMPOUND
PERC NIST Chemistry WebBook
Perchloroethylene KEGG COMPOUND
perchloroéthylène ChEBI
PERK ChemIDplus
Tetrachloräthen ChEBI
tetrachlorethylene ChemIDplus
Tetrachloroethene KEGG COMPOUND
tetrachloroethene UniProt
tétrachloroéthylène ChEBI
tetrachloroethylene ChemIDplus
Manual Xrefs Databases
3587 DrugCentral
c0004 UM-BBD
C06789 KEGG COMPOUND
HMDB0041980 HMDB
LSM-37168 LINCS
Tetrachloroethene Wikipedia
TETRACHLOROETHENE MetaCyc
View more database links
Registry Numbers Types Sources
101142 Gmelin Registry Number Gmelin
127-18-4 CAS Registry Number ChemIDplus
127-18-4 CAS Registry Number NIST Chemistry WebBook
1304635 Reaxys Registry Number Reaxys
Citations
Last Modified
13 November 2017