(R)-pantothenic acid (CHEBI:46905)

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ChEBI Name	(R)-pantothenic acid

ChEBI ID	CHEBI:46905

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

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

InChIKey

GHOKWGTUZJEAQD-ZETCQYMHSA-N

SMILES

CC(C)(CO)[C@@H](O)C(=O)NCCC(O)=O

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 ) cofactor 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. geroprotector Any compound that supports healthy aging, slows the biological aging process, or extends lifespan. nutraceutical 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 )

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)

IUPAC Name

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
PANTOTHENOIC ACID	PDBeChem
vitamin B₅	ChemIDplus

Last Modified

28 October 2021