推薦產品
化驗
≥98.0% (HPLC)
形狀
lumps
官能基
chloro
nitro
SMILES 字串
[O-][N+](=O)c1cc(c(Cl)c(c1)[N+]([O-])=O)[N+]([O-])=O
InChI
1S/C6H2ClN3O6/c7-6-4(9(13)14)1-3(8(11)12)2-5(6)10(15)16/h1-2H
InChI 密鑰
HJRJRUMKQCMYDL-UHFFFAOYSA-N
其他說明
用 ~15% 的水润湿
訊號詞
Danger
危險分類
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Sol. 1
安全危害
儲存類別代碼
4.1B - Flammable solid hazardous materials
水污染物質分類（WGK）
WGK 2
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
M Hagiyama et al.
The British journal of dermatology, 168(4), 771-778 (2012-10-31)
Neuroimmunological disorders are involved in the pathogenesis of atopic dermatitis (AD), partly through enhanced sensory nerve-skin mast cell interaction. Cell adhesion molecule 1 (CADM1) is a mast-cell adhesion molecule that mediates the adhesion to, and communication with, sympathetic nerves. To
Eujin Cho et al.
Journal of ethnopharmacology, 145(1), 294-302 (2012-11-15)
Korean red ginseng (KRG) has been shown to possess various biological activities including anti-inflammatory properties. We aimed to investigate the effects and mechanism of KRG on the prevention of atopic dermatitis (AD) using a mouse model. The effect of KRG
Atsuto Ogata et al.
International immunopharmacology, 11(10), 1628-1632 (2011-06-07)
A chymase inhibitor SUN13834 has been shown to improve skin condition in animal models for atopic dermatitis. In the present study, effective dosages of SUN13834 for atopic dermatitis patients were predicted by pharmacokinetic/pharmacodynamic (PK/PD) analyses of SUN13834 in NC/Nga mice
Andreas Natsch et al.
Chemical research in toxicology, 24(11), 2018-2027 (2011-10-26)
The skin sensitization potency of chemicals is partly related to their reactivity to proteins. This can be quantified as the rate constant of the reaction with a model peptide, and a kinetic profiling approach to determine rate constants was previously
L A Smyth et al.
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 17(1), 60-68 (2016-08-09)
Understanding the evolution of the direct and indirect pathways of allorecognition following tissue transplantation is essential in the design of tolerance-promoting protocols. On the basis that donor bone marrow-derived antigen-presenting cells are eliminated within days of transplantation, it has been
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