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28541-83-5,MFCD00067662
Catalog No.:AA002VLM

28541-83-5 | 4-Methylumbelliferyl-alpha-d-mannopyranoside

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25mg
95
in stock  
$93.00   $65.00
- +
100mg
95%
in stock  
$211.00   $148.00
- +
250mg
95%
in stock  
$411.00   $288.00
- +
1g
95%
in stock  
$1,009.00   $706.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA002VLM
Chemical Name:
4-Methylumbelliferyl-alpha-d-mannopyranoside
CAS Number:
28541-83-5
Molecular Formula:
C16H18O8
Molecular Weight:
338.3093
MDL Number:
MFCD00067662
SMILES:
OC[C@H]1O[C@H](Oc2ccc3c(c2)oc(=O)cc3C)[C@H]([C@H]([C@@H]1O)O)O
Properties
Properties
 
BP:
626.9°C at 760 mmHg  
Form:
Solid  
MP:
190 °C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
506  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
5  
Heavy Atom Count:
24  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
4  
Rotatable Bond Count:
3  
XLogP3:
-0.8  

Downstream Synthesis Route

[1]Locationinpatent:experimentalpartTouisni,Nadia;Maresca,Alfonso;McDonald,PaulC.;Lou,Yuanmei;Scozzafava,Andrea;Dedhar,Shoukat;Winum,Jean-Yves;Supuran,ClaudiuT.[JournalofMedicinalChemistry,2011,vol.54,#24,p.8271-8277]

[2]Wei,Xianhu;Ma,Yanxia;Wu,Qingping;Zhang,Jumei;Cai,Zhihe;Lu,Mianfei;Ferro,Vito[Molecules,2015,vol.20,#12,p.21681-21699]

[3]CurrentPatentAssignee:GUANGDONGACADEMYOFSCIENCES;GUANGDONGHUANKAIMICROBIALSCI&TECHNOLOGYCOLTD-CN104926898,2018,BLocationinpatent:Paragraph0084;0085

[4]Park,Sungjin;Shin,Injae[OrganicLetters,2007,vol.9,#4,p.619-622]

[5]CurrentPatentAssignee:UNIVERSITYOFMONTPELLIER;CENTRENATIONALDELARECHERCHESCIENTIFIQUE-WO2012/70024,2012,A1Locationinpatent:Page/Pagecolumn22-29

[1]Park,Sungjin;Shin,Injae[OrganicLetters,2007,vol.9,#4,p.619-622]

2,3,4,6-tetra-O-acetyl-α-D-mannopyranosylchloride 
  28541-83-5 

[1]Park,Sungjin;Shin,Injae[OrganicLetters,2007,vol.9,#4,p.619-622]

D-Mannosepentaacetate 
  28541-83-5 

[1]Touisni,Nadia;Maresca,Alfonso;McDonald,PaulC.;Lou,Yuanmei;Scozzafava,Andrea;Dedhar,Shoukat;Winum,Jean-Yves;Supuran,ClaudiuT.[JournalofMedicinalChemistry,2011,vol.54,#24,p.8271-8277]

[2]CurrentPatentAssignee:UNIVERSITYOFMONTPELLIER;CENTRENATIONALDELARECHERCHESCIENTIFIQUE-WO2012/70024,2012,A1

Literature

Title: Glycosyl coumarin carbonic anhydrase IX and XII inhibitors strongly attenuate the growth of primary breast tumors.

Journal: Journal of medicinal chemistry 20111222

Title: Structure-based drug design and optimization of mannoside bacterial FimH antagonists.

Journal: Journal of medicinal chemistry 20100624

Title: Class II alpha-mannosidase from Aspergillus fischeri: energetics of catalysis and inhibition.

Journal: International journal of biological macromolecules 20090101

Title: Role of concanavalin A lectin in recognition of pterygium remnant after surgical excision: preliminary results of a prospective study.

Journal: Indian journal of ophthalmology 20070101

Title: Molecular cloning and expression of an alpha-mannosidase gene in Mycobacterium tuberculosis.

Journal: Microbial pathogenesis 20010101

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SDS
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Tags:28541-83-5 Molecular Formula|28541-83-5 MDL|28541-83-5 SMILES|28541-83-5 4-Methylumbelliferyl-alpha-d-mannopyranoside