InChI
1S/C10H6N4O2/c15-9-7-8(13-10(16)14-9)12-6-4-2-1-3-5(6)11-7/h1-4H,(H2,12,13,14,15,16)
SMILES string
O=C1NC(=O)c2nc3ccccc3nc2N1
InChI key
HAUGRYOERYOXHX-UHFFFAOYSA-N
form
solid
color
yellow
solubility
DMSO: 11 mg/mL, dilute aqueous base: 4 mg/mL, H2O: insoluble, dilute aqueous acid: insoluble, ethanol: insoluble
Gene Information
human ... ADORA1(134), ADORA2A(135), ADORA2B(136)
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Biochem/physiol Actions
选择性 A2B 腺苷受体拮抗剂。
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
188.6 °F - Solvent
flash_point_c
87 °C - Solvent
法规信息
新产品
此项目有
B T Liang et al.
Circulation research, 76(2), 242-251 (1995-02-01)
Adenosine exerts pronounced biological effects in the heart cell. The role of multiple adenosine receptor subtypes in regulating the heart cell function is not known. Ventricular cells cultured from chick embryos 14 days in ovo were used to study a
L E Brackett et al.
Biochemical pharmacology, 47(5), 801-814 (1994-03-02)
The adenosine (ADO) receptor in NIH 3T3 fibroblasts was characterized using a series of adenosine agonists and selected xanthine and non-xanthine antagonists. The ADO receptor elicited accumulations of cyclic AMP in intact NIH 3T3 fibroblasts and caused activation of adenylate
Patrizia Minetti et al.
Journal of medicinal chemistry, 48(22), 6887-6896 (2005-10-28)
Two types of adenosine receptor ligands were designed, i.e., 9H-purine and 1H-imidazo[4,5-c]pyridines, to obtain selective A(2A) antagonists, and we report here their synthesis and binding affinities for the four adenosine receptor subtypes A(1), A(2A), A(2B) and A(3). The design was
Phedias Diamandis et al.
Nature chemical biology, 3(5), 268-273 (2007-04-10)
The identification of self-renewing and multipotent neural stem cells (NSCs) in the mammalian brain holds promise for the treatment of neurological diseases and has yielded new insight into brain cancer. However, the complete repertoire of signaling pathways that governs the
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