4-Aminophenyl α-D-mannopyranoside

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Names

[ CAS No. ]:
34213-86-0

[ Name ]:
4-Aminophenyl α-D-mannopyranoside

[Synonym ]:
(2R,3S,4S,5S,6R)-2-(4-aminophenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
4-aminophenyl |A-d-mannopyranoside
p-AmPh mannose
4-Aminophenylmannoside
p-aminophenyl alpha-D-mannoside

Chemical & Physical Properties

[ Density]:
1.517g/cm3

[ Boiling Point ]:
555.9ºC at 760mmHg

[ Melting Point ]:
165-166ºC

[ Molecular Formula ]:
C12H17NO6

[ Molecular Weight ]:
271.26600

[ Flash Point ]:
290ºC

[ Exact Mass ]:
271.10600

[ PSA ]:
125.40000

[ Index of Refraction ]:
1.662

[ Storage condition ]:
2-8°C

[ Water Solubility ]:
H2O: soluble

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 4-Nitrophenyl α-D-mannopyranoside
  • 4-Nitrophenyl 2,3,4,6-Tri-O-acetyl-α-D-mannopyranoside
  • 4-Nitrophenol
  • beta-d-glucose pentaacetate
  • 2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOSE

DownStream

Articles

Bovine serum albumin with glycated carboxyl groups shows membrane-perturbing activities.

Arch. Biochem. Biophys. 564 , 43-51, (2014)

The aim of the present study aimed to investigate whether glycated bovine serum albumin (BSA) showed novel activities on the lipid-water interface. Mannosylated BSA (Man-BSA) was prepared by modificat...

Liposomes modified with p-aminophenyl-α-D-mannopyranoside: a promising delivery system in targeting the brain.

Ther. Deliv. 4(12) , 1475-7, (2013)

Dual-targeting daunorubicin liposomes improve the therapeutic efficacy of brain glioma in animals.

J. Control. Release 141(2) , 183-92, (2010)

Chemotherapy for brain glioma has been of limited value due to the inability of transport of drug across the blood-brain barrier (BBB) and poor penetration of drug into the tumor. For overcoming these...


More Articles

Related Compounds

  • 6-(Tert-butylamino)pyridine-2-carboxamidine
  • (4-((tert-Butylthio)methyl)phenyl)boronic acid
  • 2-(2-Ethoxyethoxy)-4-methyl-3-pyridinamine
  • tert-butyl N-[1-(2H-1,2,3,4-tetrazol-5-yl)ethyl]carbamate
  • 3-(4-(Trifluoromethyl)piperidin-1-yl)propan-1-ol
  • CID 62223491
  • 1-Tert-butyl-1,3-dihydro-2lambda6,1,3-benzothiadiazole-2,2-dione
  • 4-(2-Hydroxypropyl)-2,6-dimethylphenol
  • 2,2-Dimethyl-3-(3-nitrophenyl)propanoic acid
  • Ethyl 1-(fluoromethyl)cyclohexane-1-carboxylate
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