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390607

Sigma-Aldrich

1-Adamantanecarboxamide

97%

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About This Item

Empirical Formula (Hill Notation):
C11H17NO
CAS Number:
5511-18-2
Molecular Weight:
179.26
MDL number:
MFCD00077200
UNSPSC Code:
12352100
PubChem Substance ID:
24864332
NACRES:
NA.22

assay

97%

form

powder

mp

188-190 °C (lit.)

functional group

amide

SMILES string

NC(=O)C12C[C@H]3C[C@H](C[C@H](C3)C1)C2

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-

InChI key

CKBZJTAMRPPVSR-KJZNFTALSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
STBD2908V
STBD2571V
STBD1164V
5260831
07828JZ

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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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