CHEBI:27907 - α-L-rhamnopyranose

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name α-L-rhamnopyranose
ChEBI ID CHEBI:27907
ChEBI ASCII Name alpha-L-rhamnopyranose
Definition An L-rhamnopyranose having α-configuration at the anomeric centre.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:45460, CHEBI:45196, CHEBI:10293, CHEBI:22425
Supplier Information
Download Molfile XML SDF
Formula C6H12O5
Net Charge 0
Average Mass 164.15648
Monoisotopic Mass 164.068
InChI InChI=1S/C6H12O5/c1-2-3(7)4(8)5(9)6(10)11-2/h2-10H,1H3/t2-,3-,4+,5+,6+/m0/s1
InChIKey SHZGCJCMOBCMKK-HGVZOGFYSA-N
SMILES C[C@@H]1O[C@@H](O)[C@H](O)[C@H](O)[C@H]1O
Roles Classification
Biological Role(s): epitope
The biological role played by a material entity when bound by a receptor of the adaptive immune system. Specific site on an antigen to which an antibody binds.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
(via rhamnose )
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
(via rhamnose )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing α-L-rhamnopyranose (CHEBI:27907) has role epitope (CHEBI:53000)
α-L-rhamnopyranose (CHEBI:27907) is a L-rhamnopyranose (CHEBI:62346)
Incoming 2ʼʼ-acetylpetiolaroside (CHEBI:67932) has functional parent α-L-rhamnopyranose (CHEBI:27907)
2-O-acetyl-α-L-rhamnose (CHEBI:59422) has functional parent α-L-rhamnopyranose (CHEBI:27907)
2-O-methyl-α-L-rhamnose (CHEBI:139586) has functional parent α-L-rhamnopyranose (CHEBI:27907)
2-O-sulfo-3,4-di-O-methyl-α-L-rhamnose (CHEBI:60399) has functional parent α-L-rhamnopyranose (CHEBI:27907)
3'-O-methyltricetin 3-O-α-L-rhamnopyranoside (CHEBI:75762) has functional parent α-L-rhamnopyranose (CHEBI:27907)
3,4-di-O-methyl-α-L-rhamnose (CHEBI:60398) has functional parent α-L-rhamnopyranose (CHEBI:27907)
3-O-methyl-α-L-rhamnose (CHEBI:44042) has functional parent α-L-rhamnopyranose (CHEBI:27907)
4-O-methyl-α-L-rhamnopyranose (CHEBI:59368) has functional parent α-L-rhamnopyranose (CHEBI:27907)
8-hydrazinocarbonyloctyl 2-O-methyl-α-L-rhamnoside (CHEBI:139594) has functional parent α-L-rhamnopyranose (CHEBI:27907)
fruticoside E (CHEBI:67588) has functional parent α-L-rhamnopyranose (CHEBI:27907)
icariside II (CHEBI:82619) has functional parent α-L-rhamnopyranose (CHEBI:27907)
petiolaroside (CHEBI:67931) has functional parent α-L-rhamnopyranose (CHEBI:27907)
petiolaroside decaacetate (CHEBI:67933) has functional parent α-L-rhamnopyranose (CHEBI:27907)
quercetin 7-O-α-L-rhamnopyranoside (CHEBI:76057) has functional parent α-L-rhamnopyranose (CHEBI:27907)
α-L-rhamnosyl group (CHEBI:73211) is substituent group from α-L-rhamnopyranose (CHEBI:27907)
IUPAC Names
6-deoxy-α-L-mannopyranose
α-L-rhamnopyranose
Synonyms Sources
alpha-6-Deoxy-L-mannose KEGG COMPOUND
alpha-L-Mannomethylose KEGG COMPOUND
α-L-Rha JCBN
alpha-L-Rhamnose KEGG COMPOUND
α-L-rhamnose UniProt
α-L-rhamnose ChEBI
α-L-Rhap ChEBI
Manual Xrefs Databases
C00001129 KNApSAcK
C02476 KEGG COMPOUND
RAM PDBeChem
View more database links
Registry Number Type Source
1680354 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
19443021 PubMed citation Europe PMC
23795894 PubMed citation Europe PMC
23836132 PubMed citation Europe PMC
25568069 PubMed citation Europe PMC
27091615 PubMed citation Europe PMC
7521740 PubMed citation Europe PMC
Last Modified
06 February 2018