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关于此项目
经验公式(希尔记法):
C17H20N4O5S
化学文摘社编号:
分子量:
392.43
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352202
MDL number:
InChI
1S/C17H20N4O5S/c1-3-9-20-15-13(16(22)21(10-4-2)17(20)23)18-14(19-15)11-5-7-12(8-6-11)27(24,25)26/h5-8H,3-4,9-10H2,1-2H3,(H,18,19)(H,24,25,26)
SMILES string
CCCN1C(=O)N(CCC)c2nc([nH]c2C1=O)-c3ccc(cc3)S(O)(=O)=O
InChI key
IWALGNIFYOBRKC-UHFFFAOYSA-N
form
powder
color
white
solubility
DMSO: 5 mg/mL, clear
Quality Level
Gene Information
human ... ADORA1(134), ADORA2B(136), ADORA3(140)
rat ... Adora1(29290), Adora2a(25369), Adora3(25370)
Biochem/physiol Actions
Water soluble adenosine receptor antagonist with slight selectivity for A1 receptors.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Edwin K Jackson et al.
American journal of physiology. Renal physiology, 303(7), F1000-F1005 (2012-08-10)
A(1) receptors may participate in renal sympathetic neurotransmission by enhancing the postjunctional effects of norepinephrine. The purpose of this study was to test this concept using A(1) receptor knockout (A(1)AR-/-) mice. In isolated kidneys from nontransgenic mice perfused with Tyrode's
Edwin K Jackson et al.
The Journal of pharmacology and experimental therapeutics, 307(3), 888-896 (2003-10-16)
Adenosine regulates tubular transport in collecting ducts (CDs); however, the sources of adenosine that modulate ion transport in CDs are unknown. The extracellular cAMP-adenosine pathway refers to the conversion of cAMP to AMP by ectophosphodiesterase, followed by metabolism of AMP
Edwin K Jackson et al.
The Journal of pharmacology and experimental therapeutics, 320(1), 117-123 (2006-10-10)
The extracellular cAMP-adenosine pathway is the cellular egress of cAMP followed by extracellular conversion of cAMP to adenosine by the sequential actions of ecto-phosphodiesterase and ecto-5'-nucleotidase. Although detailed studies in isolated organs, tissues, and cells provide evidence for an extracellular
Manuela Morato et al.
European journal of pharmacology, 455(2-3), 135-141 (2002-11-26)
The renin-angiotensin system may be involved in hypertension induced by adenosine receptors blockade with 1,3-dipropyl-8-sulfophenylxanthine (DPSPX). Contractions of the mesenteric vasculature to angiotensin II, noradrenaline and potassium chloride were studied in DPSPX-induced hypertension. Male Wistar rats received infusions of saline
Adenosine-dopamine interactions and ventilation mediated through carotid body chemoreceptors.
E C Monteiro et al.
Advances in experimental medicine and biology, 475, 671-684 (2000-06-13)
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