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102822-56-0

102822-56-0 Structure

102822-56-0 Structure
IdentificationBack Directory
[Name]

MANNOSTATIN A, HYDROCHLORIDE
[CAS]

102822-56-0
[Synonyms]

mannostatin
mannostatina
5-beta))-4-alph
MANNOSTATIN A HCL
MANNOSTATIN A, HYDROCHLORIDE
(1R)-4α-Methylthio-5β-aminocyclopentane-1β,2β,3β-triol
(1R)-5β-Methylthio-4α-aminocyclopentane-1α,2α,3α-triol
(1R)-4α-Amino-5β-(methylthio)-1α,2α,3α-cyclopentanetriol
1,2,3-Cyclopentanetriol, 4-amino-5-(methylthio)-, (1R,2R,3R,4S,5R)-
1,2,3-cyclopentanetriol,4-amino-5-(methylthio)-,(1r-(1-alpha,2-alpha,3-alpha,
[Molecular Formula]

C6H13NO3S
[MDL Number]

MFCD00270023
[MOL File]

102822-56-0.mol
[Molecular Weight]

179.24
Chemical PropertiesBack Directory
[Boiling point ]

329.4±42.0 °C(Predicted)
[density ]

1.45±0.1 g/cm3(Predicted)
[pka]

13.51±0.70(Predicted)
Hazard InformationBack Directory
[Definition]

ChEBI: Mannostatin A is an amino cyclitol that is cyclopentane substituted by hydroxy groups at positions 1, 2 and 3, by an amino group at positon 4, and by a methylsulfanediyl group at position 5 (the 1R,2R,3R,4S,5R-stereoisomer). It is isolated from the soil bacterium Streptoverticillium verticillium. It has a role as an EC 3.2.1.24 (alpha-mannosidase) inhibitor, a bacterial metabolite and an EC 3.2.1.114 (mannosyl-oligosaccharide 1,3-1,6-alpha-mannosidase) inhibitor. It is a methyl sulfide, a triol and an amino cyclitol.
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