Services
Research
Training
Industry
About us
ChEBI
Examples:
iron*
,
InChI=1S/CH4O/c1-2/h2H,1H3
,
caffeine
Advanced
Home
Advanced Search
Browse
Documentation
Download
Tools
About ChEBI
Submit
Contact us
DiNA
Statistics
Entity of the Month
Periodic Table
Ontology
Train online
User Manual
Annotation Manual
Developer Manual
FAQ's
BiNChE
libChEBI
Web Services
ChEBI
> Main
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
Find compounds which contain this structure
Find compounds which resemble this structure
Take structure to the Advanced Search
Formula
C6H12O5
Net Charge
0
Average Mass
164.15648
Monoisotopic Mass
164.06847
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
6-deoxy-α-
L
-mannopyranose
ChEBI
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
-Rha
p
ChEBI
WURCS=2.0/1,1,0/[a2211m-1a_1-5]/1/
GlyTouCan
Manual Xrefs
Databases
C00001129
KNApSAcK
C02476
KEGG COMPOUND
G38999IM
GlyTouCan
G38999IM
GlyGen
RAM
PDBeChem
View more database links
Registry Number
Type
Source
1680354
Reaxys Registry Number
Reaxys
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
31537530
PubMed citation
Europe PMC
36988069
PubMed citation
Europe PMC
7521740
PubMed citation
Europe PMC
Last Modified
03 May 2023