288225
氯(三乙基膦)金(I)
97%, solid
别名:
(三乙基膦)氯化金(I)
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关于此项目
线性分子式:
(C2H5)3PAuCl
化学文摘社编号:
分子量:
350.58
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
EC Number:
239-572-3
MDL number:
产品名称
氯(三乙基膦)金(I), 97%
InChI key
SYBBXLKWGHAVHP-UHFFFAOYSA-M
InChI
1S/C6H15P.Au.ClH/c1-4-7(5-2)6-3;;/h4-6H2,1-3H3;;1H/q;+1;/p-1
SMILES string
Cl[Au].CCP(CC)CC
assay
97%
form
solid
reaction suitability
core: gold
reagent type: catalyst
bp
210 °C/0.03 mmHg (lit.)
mp
84-86 °C (lit.)
Quality Level
Application
signalword
Danger
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
P Davis et al.
Arthritis and rheumatism, 26(1), 82-86 (1983-01-01)
The effect of sodium aurothiomalate and triethylphosphine gold on the generation of superoxide radicals by chemotactic tripeptide-activated polymorphonuclear leukocytes has been investigated using a cytochrome C reduction technique. Neither gold compound inhibited the binding of the tripeptide to cells. Sodium
S K Mallya et al.
Biochemical and biophysical research communications, 144(1), 101-108 (1987-04-14)
Six gold(I) salts, some of which are used as drugs in chrysotherapy, are shown to be inhibitors of two forms of human neutrophil collagenase. The IC50 values vary over six orders of magnitude, the lowest being 3.5 nM for Myocrisin.
C J Kirkpatrick et al.
Rheumatology international, 3(2), 49-56 (1983-01-01)
Chondrocyte structure and function under the influence of two gold-containing therapeutic agents, aurothioglucose and triethylphosphine gold, were studied in a monolayer culture system for cultivating lapine articular chondrocytes. The functional parameters investigated were chondrocyte proliferation and the incorporation of 35SO4
R M Snyder et al.
Molecular pharmacology, 32(3), 437-442 (1987-09-01)
Auranofin (AF) is an orally active chrysotherapeutic agent used for the treatment of rheumatoid arthritis, a self-perpetuating inflammatory disease. Because of reports suggesting that AF and other gold complexes can, under certain circumstances, exacerbate rheumatoid inflammatory lesions in humans and
R M Snyder et al.
Biochemical pharmacology, 36(5), 647-654 (1987-03-01)
Auranofin (AF) is an orally active chrysotherapeutic agent whose precise mechanism of action with its putative target cell, the macrophage, is not known. In a previous paper, we described a sequential thiol exchange mechanism that explained auranofin's molecular mechanism of
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