HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
Huagongshe Open Program:[email protected]AI access: llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.7.8
  1. Home
  2. /Compound

4-Amino-5-(methylsulfanyl)cyclopentane-1,2,3-triol

HCID 124189
NotesReactions

Completing data — refresh the page later to see the latest

Basic informationNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
102822-56-0
Standard SMILES
CS[C@@H]1[C@@H](N)[C@@H](O)[C@@H](O)[C@H]1O
InChIKey
BLOFGONIVNXZME-YDMGZANHSA-N
Molecular formula
C6H13NO3S
Average molar mass
179.241 g/mol
Monoisotopic mass
179.06161428

Names & identifiers

Preferred name
4-Amino-5-(methylsulfanyl)cyclopentane-1,2,3-triol
IUPAC
(1R,2R,3R,4S,5R)-4-Amino-5-(methylsulfanyl)cyclopentane-1,2,3-triol
English name
Mannostatin a, hydrochloride
Molecular formula
C6H13NO3S
Molecular weight
179.24

Names & synonyms

mannostatinmannostatina5-beta))-4-alphMANNOSTATIN A HCLMannostatin a, hydrochloride(1R)-5β-Methylthio-4α-aminocyclopentane-1α,2α,3α-triol(1R)-4α-Methylthio-5β-aminocyclopentane-1β,2β,3β-triol(1R)-4α-Amino-5β-(methylthio)-1α,2α,3α-cyclopentanetriol1,2,3-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,

Database identifiers

CAS
102822-56-0
PubChem CID
124189
DTXSID
DTXSID20908059
ChEMBL
CHEMBL9623
ChEBI
CHEBI:191195
Nikkaji
J404.621H

Properties

Physicochemical properties

Boiling point
329.4 · 329.4±42.0 °C(Predicted)
Density
1.45 · 1.45±0.1 g/cm3(Predicted)
pka
13.51 · 13.51±0.70(Predicted)

Chemistry & industry

Suppliers2 total

武汉易泰科技有限公司上海分公司18930552037 · [email protected]
BOC Sciences+1-631-485-4226 · [email protected]
Additional notes · 1 item

DefinitionChEBI: 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.

Related reactions

0 records
New reaction record

No reaction records under the current filter.

Compound notes

Loading…

On this pageBasic informationNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes