CHEBI:46905 - (R)-pantothenic acid

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ChEBI Name (R)-pantothenic acid
ChEBI ASCII Name (R)-pantothenic acid
Definition A pantothenic acid having R-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:44679, CHEBI:18701
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Formula C9H17NO5
Net Charge 0
Average Mass 219.23502
Monoisotopic Mass 219.11067
InChI InChI=1S/C9H17NO5/c1-9(2,5-11)7(14)8(15)10-4-3-6(12)13/h7,11,14H,3-5H2,1-2H3,(H,10,15)(H,12,13)/t7-/m0/s1
Metabolite of Species Details
Chlamydomonas reinhardtii (NCBI:txid3055) From MetaboLights See: MetaboLights Study
Chlamydomonas reinhardtii (NCBI:txid3055) From MetaboLights See: MetaboLights Study
Glycine max (NCBI:txid3847) From MetaboLights See: MetaboLights Study
Homo sapiens (NCBI:txid9606) Found in blood serum (BTO:0000133). See: MetaboLights Study
Homo sapiens (NCBI:txid9606) Found in blood serum (BTO:0000133). From MetaboLights See: MetaboLights Study
Homo sapiens (NCBI:txid9606) Found in blood serum (BTO:0000133). From MetaboLights See: MetaboLights Study
Roles Classification
Biological Role(s): human blood serum metabolite
Any metabolite (endogenous or exogenous) found in human blood serum samples.
water-soluble vitamin (role)
Any vitamin that dissolves in water and readily absorbed into tissues for immediate use. Unlike the fat-soluble vitamins, they are not stored in the body and need to be replenished regularly in the diet and will rarely accumulate to toxic levels since they are quickly excreted from the body via urine.
(via B vitamin )
(via pantothenic acids )
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via pantothenic acid )
An organic molecule or ion (usually a metal ion) that is required by an enzyme for its activity. It may be attached either loosely (coenzyme) or tightly (prosthetic group).
(via pantothenic acids )
Application(s): antidote to curare poisoning
A role borne by a molecule that acts to counteract or neutralize the deleterious effects of curare.
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
A product in capsule, tablet or liquid form that provide essential nutrients, such as a vitamin, an essential mineral, a protein, an herb, or similar nutritional substance.
(via B vitamin )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (R)-pantothenic acid (CHEBI:46905) has role antidote to curare poisoning (CHEBI:74530)
(R)-pantothenic acid (CHEBI:46905) has role geroprotector (CHEBI:176497)
(R)-pantothenic acid (CHEBI:46905) has role human blood serum metabolite (CHEBI:85234)
(R)-pantothenic acid (CHEBI:46905) is a pantothenic acid (CHEBI:7916)
(R)-pantothenic acid (CHEBI:46905) is a vitamin B5 (CHEBI:176840)
(R)-pantothenic acid (CHEBI:46905) is conjugate acid of (R)-pantothenate (CHEBI:29032)
Incoming (R)-4'-phosphonatopantothenate(3−) (CHEBI:10986) has functional parent (R)-pantothenic acid (CHEBI:46905)
(R)-4'-phosphopantothenate(1−) (CHEBI:12886) has functional parent (R)-pantothenic acid (CHEBI:46905)
(R)-4'-phosphopantothenate(2−) (CHEBI:20891) has functional parent (R)-pantothenic acid (CHEBI:46905)
(R)-4'-phosphopantothenic acid (CHEBI:15905) has functional parent (R)-pantothenic acid (CHEBI:46905)
vitamin B complex (CHEBI:75782) has part (R)-pantothenic acid (CHEBI:46905)
(R)-pantothenate (CHEBI:29032) is conjugate base of (R)-pantothenic acid (CHEBI:46905)
3-[(2R)-2,4-dihydroxy-3,3-dimethylbutanamido]propanoic acid
Synonyms Sources
(+)-Pantothenic acid HMDB
(R)-N-(2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)-β-alanine ChemIDplus
chick antidermatitis factor ChemIDplus
D(+)-N-(2,4-dihydroxy-3,3-dimethylbutyryl)-β-alanine ChemIDplus
D-(+)-pantothenic acid ChEBI
D-pantothenic acid ChemIDplus
N-[(2R)-2,4-dihydroxy-3,3-dimethylbutanoyl]-beta-alanine PDBeChem
Pantothenic acid KEGG COMPOUND
vitamin B5 ChemIDplus
Manual Xrefs Databases
2055 DrugCentral
C00001550 KNApSAcK
DB01783 DrugBank
FDB008322 FooDB
HMDB0000210 HMDB
Pantothenic_Acid Wikipedia
View more database links
Registry Numbers Types Sources
1727064 Beilstein Registry Number ChemIDplus
1727064 Reaxys Registry Number Reaxys
79-83-4 CAS Registry Number NIST Chemistry WebBook
79-83-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
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Last Modified
28 October 2021