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Merck

C9694

Sigma-Aldrich

8-环戊基-1,3-二丙基黄嘌呤

别名:

1,3-二丙基-8-环戊基黄嘌呤, DPCPX, PD 116948

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About This Item

经验公式(希尔记法):
C16H24N4O2
分子量:
304.39
MDL號碼:
分類程式碼代碼:
12352200

价格与库存信息目前不能提供

儲存溫度

2-8°C

SMILES 字串

CCCN1C(=O)N(CCC)c2nc([nH]c2C1=O)C3CCCC3

InChI

1S/C16H24N4O2/c1-3-9-19-14-12(15(21)20(10-4-2)16(19)22)17-13(18-14)11-7-5-6-8-11/h11H,3-10H2,1-2H3,(H,17,18)

InChI 密鑰

FFBDFADSZUINTG-UHFFFAOYSA-N

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生化/生理作用

Selective A1 adenosine receptor antagonist

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说明
价格

象形圖

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訊號詞

Warning

危險聲明

危險分類

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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R J Knight et al.
British journal of pharmacology, 109(1), 271-277 (1993-05-01)
1. The diuretic effect of the selective A1 adenosine receptor antagonist, 8-cyclopentyl-1,3-dipropylxanthine (CPX), was investigated in anaesthetized rats. 2. CPX (0.1 mg kg-1, i.v.) produced significant increases in urine flow, and the excretion rate and fractional excretion of both sodium
Leonardo M Crema et al.
Physiology & behavior, 109, 1-7 (2012-11-20)
This study examined the effects of two chronic stress regimens upon depressive-like behavior, A(1) and A(2A) adenosine receptor binding and immunocontent. Male rats were subjected to unpredictable chronic mild stress (UCMS) or to chronic restraint stress (CRS) for 40 days.
Jean Liu et al.
European journal of pharmacology, 698(1-3), 213-219 (2012-11-13)
The present study explored a link between spinal 5-HT(7) and adenosine A(1) receptors in antinociception by systemic amitriptyline in normal and adenosine A(1) receptor knock-out mice using the 2% formalin test. In normal mice, antinociception by systemic amitriptyline 3mg/kg was
Famke Aeffner et al.
Journal of virology, 88(17), 10214-10227 (2014-06-27)
We have shown that bronchoalveolar epithelial A1-adenosine receptors (A1-AdoR) are activated in influenza A virus-infected mice. Alveolar macrophages and neutrophils also express A1-AdoRs, and we hypothesized that activation of A1-AdoRs on these cells will promote macrophage and neutrophil chemotaxis and
G Taccola et al.
Neuroscience, 222, 191-204 (2012-07-25)
It is not well-studied how the ubiquitous neuromodulator adenosine (ADO) affects mammalian locomotor network activities. We analyzed this here with focus on roles of 8-cyclopentyl-1,3-dipropylxanthine (DPCPX)-sensitive A(1)-type ADO receptors. For this, we recorded field potentials from ventral lumbar nerve roots

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