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DEOXYMANNOJIRIMYCIN

DEOXYMANNOJIRIMYCIN structure

DEOXYMANNOJIRIMYCIN 

structure
  • CAS No:

    84444-90-6

  • Formula:

    C6H13NO4

  • Chemical Name:

    DEOXYMANNOJIRIMYCIN

  • Synonyms:

    DEOXYMANNOJIRIMYCIN;DMJ;3,4,5-Piperidinetriol, 2-(hydroxymethyl)-, (2R,3R,4R,5R)-;1,5-Dideoxy-1,5-epimino-D-mannitol;1,5-Dideoxy-1,5-imino-D-mannitol;1-Deoxymannojirimycin;Antibiotic LU-1;LU-1

Description

selectively inhibits a-D-mannosidases 1A/B and processing of N-linked glycoproteins, competitive, active site-directed inhibitor of mammalian Golgi a-D-mannosidase I


An alpha-glucosidase inhibitor with antiviral action. Derivatives of deoxynojirimycin may have anti-HIV activity.

DEOXYMANNOJIRIMYCIN Basic Attributes

163.17

163.08400

Characteristics

92.95000

1.456g/cm3

361.1ºC at 760 mmHg

197.3ºC

1.582

2-8°C

Safety Information

3

20/21/22

36

Xn

Drug Information

Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly. (See all compounds classified as Antiviral Agents.)|Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. (See all compounds classified as Enzyme Inhibitors.)

1 Deoxymannojirimycin

DEOXYMANNOJIRIMYCIN Use and Manufacturing

competitive inhibitor of glucosidase I and II; pig kidney trehalase inhibitor

Computed Properties

Molecular Weight:163.17
XLogP3:-2.3
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:163.08445790
Monoisotopic Mass:163.08445790
Topological Polar Surface Area:93
Heavy Atom Count:11
Complexity:132
Defined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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