Quality Level
assay
99%
mp
>300 °C (lit.)
functional group
amine
SMILES string
Cl.C[C@H](N)C12C[C@H]3C[C@H](C[C@H](C3)C1)C2
InChI
1S/C12H21N.ClH/c1-8(13)12-5-9-2-10(6-12)4-11(3-9)7-12;/h8-11H,2-7,13H2,1H3;1H/t8?,9-,10+,11-,12-;
InChI key
OZBDFBJXRJWNAV-MZHJCFSPSA-N
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Linh Tran et al.
Molecules (Basel, Switzerland), 16(12), 10227-10255 (2011-12-14)
The M2 channel protein on the influenza A virus membrane has become the main target of the anti-flu drugs amantadine and rimantadine. The structure of the M2 channel proteins of the H3N2 (PDB code 2RLF) and 2009-H1N1 (Genbank accession number
Rafal M Pielak et al.
Structure (London, England : 1993), 19(11), 1655-1663 (2011-11-15)
The M2 channel of influenza A is a target of the adamantane family antiviral drugs. Two different drug-binding sites have been reported: one inside the pore, and the other is a lipid-facing pocket. A previous study showed that a chimera
Guang-Quan Wang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 98, 275-281 (2012-09-11)
Amantadine hydrochloride (AMA) and rimantadine hydrochloride (RIM) are non-fluorescent in aqueous solutions. This property makes their determination through direct fluorescent method difficult. The competing reactions and the supramolecular interaction mechanisms between the two drugs and coptisine (COP) as they fight
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 390593-1G | 04061831972818 |