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质量水平
检测方案
99%
mp
>300 °C (lit.)
SMILES字符串
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
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Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
G G U Rohde
Der Internist, 52(9), 1047-1052 (2011-08-03)
Influenza infections have important socio-economic consequences. Risk groups identified so far include small children and elderly adults with comorbidities. In recent years in addition to seasonal influenza an outbreak of avian influenza occurred in 2005 and the new H1N1 pandemic
I T Fediakina et al.
Antibiotiki i khimioterapiia = Antibiotics and chemoterapy [sic], 56(3-4), 3-9 (2011-09-15)
The data on cytotoxicity and antiviral activity of commercial antivirals, such as Remantadine, Oseltamivir, Arbidol and Ribavirin in the MDCK cell culture infected with highly pathogenic (H5N1) and pandemic 2009 (H1N1) influenza A viruses are presented. The study of the
Tijana Ivanovic et al.
PloS one, 7(3), e31566-e31566 (2012-03-14)
M2 protein of influenza A viruses is a tetrameric transmembrane proton channel, which has essential functions both early and late in the virus infectious cycle. Previous studies of proton transport by M2 have been limited to measurements outside the context
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
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
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