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Chitoheptaose

Chitoheptaose structure

Chitoheptaose 

structure
  • CAS No:

    68232-35-9

  • Formula:

    C42H79N7O29

  • Chemical Name:

    Chitoheptaose

  • Synonyms:

    CHITOHEPTAOSE HEPTAHYDROCHLORIDE;Chitoheptaose 7HCl;Chitoheptaose Hydrochloride (or Chitoheptaose 7HCl);Chitoheptaose Hydrochloride;Chitoheptaose;O-2-Amino-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-2-amino-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-2-amino-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-2-amino-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-2-amino-2-deoxy-beta-D-glucopyranosyl-(1-4)-O-2-amino-2-deoxy-beta-D-glucopyranosyl-(1-4)-2-amino-2-deoxy-D-glucose;Chitotetraose 7HCl;D-Glucose, O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-O-2-amino-2-deoxy-β-D-glucopyranosyl-(1→4)-2-amino-2-deoxy-

  • Categories:

    Chemical Reagents  >  Organic Reagents

Chitoheptaose Basic Attributes

1146.11

1397.33000

White to off-white

29329990

Characteristics

625.81000

1.72±0.1 g/cm3(Predicted)

1408.9±65.0 °C(Predicted)

11.01±0.45(Predicted)

-20°C, stored under nitrogen

Chitoheptaose Use and Manufacturing

Used for the development of new products of oligosaccharides in the fields of medicine, food, aquaculture, modern agriculture, daily chemical and biochemical reagents; oligosaccharide inspection and analysis and quality control reference products; oligosaccharide chip preparation research; oligosaccharide and Research on protein interactions; research on structure-activity relationship and mechanism of action of oligosaccharide drugs and other fields of sugar chemistry and sugar biology.


Chitoheptaose is a chitosan oligosaccharide. Chitoheptaose is capable of extracting exoskeletons from crustaceans, such as the shells of crabs, shrimp and lobsters. Chitoheptaose has antioxidant, anti-inflammatory and anti-apoptotic activities and can be used in the study of myocarditis. Chitoheptaose has cardioprotective effects and improves cardiac parameters (left ventricular internal size, end-systolic and end-diastolic, ejection fraction and shortening fraction), inflammatory cytokines (IL-1β) in vanishing models[1].

Computed Properties

Molecular Weight:1401.3
Hydrogen Bond Donor Count:30
Hydrogen Bond Acceptor Count:36
Rotatable Bond Count:19
Exact Mass:1399.326013
Monoisotopic Mass:1397.328964
Topological Polar Surface Area:626
Heavy Atom Count:85
Complexity:1840
Defined Atom Stereocenter Count:34
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:8
Compound Is Canonicalized:Yes

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