CHEBI:67233 - 1-D-1,2-anhydro-myo-inositol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 1-D-1,2-anhydro-myo-inositol
ChEBI ID CHEBI:67233
ChEBI ASCII Name 1-D-1,2-anhydro-myo-inositol
Definition A conduritol epoxide resulting from the formal epoxidation of the double bond of (+)-conduritol B.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C6H10O5
Net Charge 0
Average Mass 162.14060
Monoisotopic Mass 162.05282
InChI InChI=1S/C6H10O5/c7-1-2(8)4(10)6-5(11-6)3(1)9/h1-10H/t1-,2-,3+,4+,5-,6+/m0/s1
InChIKey ZHMWOVGZCINIHW-FTYOSCRSSA-N
SMILES O[C@H]1[C@H](O)[C@@H](O)[C@H]2O[C@H]2[C@@H]1O
Roles Classification
Biological Role(s): EC 3.2.1.48 (sucrose alpha-glucosidase) inhibitor
An EC 3.2.1.* (glycosidase) inhibitor that interferes with the action of sucrose alpha-glucosidase (EC 3.2.1.48).
EC 3.2.1.10 (oligo-1,6-glucosidase) inhibitor
An EC 3.2.1.* (glycosidase) inhibitor that inhibits the action of sucrose oligo-1,6-glucosidase (EC 3.2.1.10).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1-D-1,2-anhydro-myo-inositol (CHEBI:67233) has functional parent (+)-conduritol B (CHEBI:67224)
1-D-1,2-anhydro-myo-inositol (CHEBI:67233) has role EC 3.2.1.10 (oligo-1,6-glucosidase) inhibitor (CHEBI:67232)
1-D-1,2-anhydro-myo-inositol (CHEBI:67233) has role EC 3.2.1.48 (sucrose α-glucosidase) inhibitor (CHEBI:67231)
1-D-1,2-anhydro-myo-inositol (CHEBI:67233) is a conduritol epoxide (CHEBI:67235)
1-D-1,2-anhydro-myo-inositol (CHEBI:67233) is enantiomer of 1-L-1,2-anhydro-myo-inositol (CHEBI:67234)
Incoming conduritol B epoxide (CHEBI:67229) has part 1-D-1,2-anhydro-myo-inositol (CHEBI:67233)
1-L-1,2-anhydro-myo-inositol (CHEBI:67234) is enantiomer of 1-D-1,2-anhydro-myo-inositol (CHEBI:67233)
IUPAC Name
(1R,2R,3S,4S,5R,6S)-7-oxabicyclo[4.1.0]heptane-2,3,4,5-tetrol
Synonyms Sources
(+)-(1R,2R,3S,4S,5R,6S)-2,3,4,5-tetraol-7-oxabicyclo[4.1.0]heptane ChEBI
(1R,2R,3S,4S,5R,6S)-2,3,4,5-tetraol-7-oxabicyclo[4.1.0]heptane ChEBI
1D-conduritol B epoxide ChEBI
Registry Number Type Source
1680620 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
560212 PubMed citation Europe PMC
Last Modified
30 August 2012