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Merck

391662

Sigma-Aldrich

(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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About This Item

经验公式(希尔记法):
C10H19N
CAS号:
分子量:
153.26
MDL號碼:
分類程式碼代碼:
12352116
PubChem物質ID:
NACRES:
NA.22

化驗

95%

光學活性

[α]22/D +44°, neat

折射率

n20/D 1.481 (lit.)

bp

90 °C/18 mmHg (lit.)

密度

0.909 g/mL at 25 °C (lit.)

SMILES 字串

C[C@@H]1[C@@H](N)C[C@H]2C[C@@H]1C2(C)C

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

InChI 密鑰

VPTSZLVPZCTAHZ-KZVJFYERSA-N

應用

(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.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

161.6 °F - closed cup

閃點(°C)

72 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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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)
Discovery of highly potent agents against influenza A virus.
Zhao X, et al.
European Journal of Medicinal Chemistry, 46(1), 52-57 (2011)
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)

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