CHEBI:18276 - dihydrogen

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name dihydrogen
ChEBI ID CHEBI:18276
Definition An elemental molecule consisting of two hydrogens joined by a single bond.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:5785, CHEBI:13350, CHEBI:25363
Supplier Information ZINC000002522619
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Deoxyuridine (dU) is a compound and a nucleoside. It belongs to a class of compounds known as Pyrimidine 2'-deoxyribonucleosides and closely resembles the chemical composition of uridine but without the presence of the 2' hydroxyl group. Idoxuridine and Trifluridine are variants of deoxyuridine used as antiviral drugs. They are similar enough to be incorporated as part of DNA replication, but they possess side groups on the uracil component (an iodine and a CF3 group, respectively), that prevent base pairing. A known use of dU is as a precursor in the synthesis of Edoxudine. This compound exists in all living organisms and can become part of DNA in both prokaryotic and eukaryotic cells through two mechanisms. The first is the removal of an amino group from cytosine to result in uracil and the second is the non-intentional incorporation of pyrimidine where thymine belongs in the DNA, resulting in dUMP. UMP synthase deficiency is a metabolic disorder in humans that involves deoxyuridine. Deoxyuridine can be toxic. It has also been found in several foods, which makes it a useful indicator for diseases through consumption of those foods.
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Formula H2
Net Charge 0
Average Mass 2.01588
Monoisotopic Mass 2.01565
InChI InChI=1S/H2/h1H
InChIKey UFHFLCQGNIYNRP-UHFFFAOYSA-N
SMILES [H][H]
Metabolite of Species Details
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
electron donor
A molecular entity that can transfer an electron to another molecular entity.
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
food packaging gas
A food additive that is a (generally inert) gas which is used to envelop foodstuffs during packing and so protect them from unwanted chemical reactions such as food spoilage or oxidation during subsequent transport and storage. The term includes propellant gases, used to expel foods from a container.
Application(s): fuel
An energy-rich substance that can be transformed with release of usable energy.
food packaging gas
A food additive that is a (generally inert) gas which is used to envelop foodstuffs during packing and so protect them from unwanted chemical reactions such as food spoilage or oxidation during subsequent transport and storage. The term includes propellant gases, used to expel foods from a container.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing dihydrogen (CHEBI:18276) has role antioxidant (CHEBI:22586)
dihydrogen (CHEBI:18276) has role electron donor (CHEBI:15022)
dihydrogen (CHEBI:18276) has role food packaging gas (CHEBI:77974)
dihydrogen (CHEBI:18276) has role fuel (CHEBI:33292)
dihydrogen (CHEBI:18276) has role human metabolite (CHEBI:77746)
dihydrogen (CHEBI:18276) is a elemental hydrogen (CHEBI:33260)
dihydrogen (CHEBI:18276) is a elemental molecule (CHEBI:25362)
dihydrogen (CHEBI:18276) is a gas molecular entity (CHEBI:138675)
Incoming dideuterium (CHEBI:29294) is a dihydrogen (CHEBI:18276)
diprotium (CHEBI:29299) is a dihydrogen (CHEBI:18276)
ditritium (CHEBI:29298) is a dihydrogen (CHEBI:18276)
H group (CHEBI:64428) is substituent group from dihydrogen (CHEBI:18276)
IUPAC Name
dihydrogen
Synonyms Sources
dihydrogen ChEBI
E 949 ChEBI
E-949 ChEBI
E949 ChEBI
H2 KEGG COMPOUND
H2 IUPAC
H2 UniProt
Hydrogen KEGG COMPOUND
molecular hydrogen ChEBI
Manual Xrefs Databases
748 MolBase
C00282 KEGG COMPOUND
HMDB0001362 HMDB
Hydrogen Wikipedia
HYDROGEN-MOLECULE MetaCyc
View more database links
Registry Numbers Types Sources
1333-74-0 CAS Registry Number KEGG COMPOUND
1333-74-0 CAS Registry Number ChemIDplus
1333-74-0 CAS Registry Number NIST Chemistry WebBook
3 Gmelin Registry Number Gmelin
3587189 Reaxys Registry Number Reaxys
Citations Types Sources
15303745 PubMed citation Europe PMC
16517646 PubMed citation Europe PMC
18706888 PubMed citation Europe PMC
19905000 PubMed citation Europe PMC
19908827 PubMed citation Europe PMC
20568549 PubMed citation Europe PMC
24171421 PubMed citation Europe PMC
Last Modified
13 October 2017