390607
1-Adamantanecarboxamide
97%
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About This Item
Empirical Formula (Hill Notation):
C11H17NO
CAS Number:
Molecular Weight:
179.26
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
powder
InChI
1S/C11H17NO/c12-10(13)11-4-7-1-8(5-11)3-9(2-7)6-11/h7-9H,1-6H2,(H2,12,13)/t7-,8+,9-,11-
SMILES string
NC(=O)C12C[C@H]3C[C@H](C[C@H](C3)C1)C2
InChI key
CKBZJTAMRPPVSR-KJZNFTALSA-N
assay
97%
form
powder
mp
188-190 °C (lit.)
functional group
amide
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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V L Andronova
Antibiotiki i khimioterapiia = Antibiotics and chemoterapy [sic], 41(7-8), 26-30 (1996-01-01)
Amide of 1-adamantane carboxylic acid (AACA), the same as remantadine, was shown to have no antiviral action and any influence on the efficiency of the Sindbis virus adsorption. However, it significantly inhibited the virus specific synthesis of RNA and protein.
L Q Gu et al.
Science (New York, N.Y.), 291(5504), 636-640 (2001-02-07)
We describe a heptameric protein pore that has been engineered to accommodate two different cyclodextrin adapters simultaneously within the lumen of a transmembrane beta barrel. The volume between the adapters is a cavity of approximately 4400 cubic angstroms. Analysis of
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