391662
(1S,2S,3S,5R)-(+)-异松莰烯胺
95%
别名:
(+)-异松莰烯胺, (1S,2S,3S,5R)-3-蒎烷胺
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关于此项目
经验公式（希尔记法）:
C10H19N
化学文摘社编号:
分子量:
153.26
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
MDL number:
Assay:
95%
InChI
1S/C10H19N/c1-6-8-4-7(5-9(6)11)10(8,2)3/h6-9H,4-5,11H2,1-3H3/t6-,7+,8-,9-/m0/s1
SMILES string
C[C@@H]1[C@@H](N)C[C@H]2C[C@@H]1C2(C)C
InChI key
VPTSZLVPZCTAHZ-KZVJFYERSA-N
assay
95%
optical activity
[α]22/D +44°, neat
refractive index
n20/D 1.481 (lit.)
bp
90 °C/18 mmHg (lit.)
density
0.909 g/mL at 25 °C (lit.)
Quality Level
Application
(1S,2S,3S,5R)-(+)-isopinocampheylamine is a primary bicyclic amine with potent M2 ion channel inhibitor ability similar to that of amantadine, making it a promising candidate for developing anti-influenza agents.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
161.6 °F - closed cup
flash_point_c
72 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
New strategy for high throughput screening of anti-influenza virus M2 ion channel inhibitors.
Li C, et al.
Current Pharmaceutical Design, 19(28), 5146-5155 (2013)
Discovery of highly potent agents against influenza A virus.
Zhao X, et al.
European Journal of Medicinal Chemistry, 46(1), 52-57 (2011)
Identification of hits as matrix-2 protein inhibitors through the focused screening of a small primary amine library.
Hu W, et al.
Journal of Medicinal Chemistry, 53(9), 3831-3834 (2010)
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