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Empirische Formel (Hill-System):
C18H22N6O4
CAS-Nummer:
Molekulargewicht:
386.41
UNSPSC Code:
12352202
PubChem Substance ID:
MDL number:
Assay:
>95%
Form:
solid
assay
>95%
form
solid
solubility
methanol: slightly soluble 0.2 mg/mL, 0.1 M HCl: 14 mg/mL, DMSO: soluble, H2O: insoluble
storage temp.
2-8°C
SMILES string
Nc1ccc(CCNc2ncnc3n(cnc23)[C@@H]4O[C@H](CO)[C@@H](O)[C@H]4O)cc1
InChI
1S/C18H22N6O4/c19-11-3-1-10(2-4-11)5-6-20-16-13-17(22-8-21-16)24(9-23-13)18-15(27)14(26)12(7-25)28-18/h1-4,8-9,12,14-15,18,25-27H,5-7,19H2,(H,20,21,22)/t12-,14-,15-,18-/m1/s1
InChI key
XTPOZVLRZZIEBW-SCFUHWHPSA-N
Gene Information
human ... ADORA3(140)
rat ... Adora1(29290), Adora2a(25369), Adora3(25370)
Biochem/physiol Actions
Wirksamer, nichtselektiver A3-Adenosinrezeptor-Agonist.
Features and Benefits
Diese Verbindung ist auf der Seite Adenosine Receptors im „Handbook of Receptor Classification and Signal Transduction“ aufgeführt. Um andere Seiten dieses Handbuchs anzuzeigen, klicken Sie bitte hier.
Lagerklasse
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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M G Collis et al.
Trends in pharmacological sciences, 14(10), 360-366 (1993-10-01)
The numerous and widespread effects of adenosine provide both an opportunity for the development of novel therapeutic agents acting via adenosine receptors and the challenge of achieving selectivity of action. The feasibility of achieving selectivity is enhanced if receptor subtypes
Adenosine A3 receptors: two into one won't go.
A M Carruthers et al.
Trends in pharmacological sciences, 14(8), 290-291 (1993-08-01)
J R Fozard et al.
British journal of pharmacology, 109(1), 3-5 (1993-05-01)
The cardiovascular effects of N6-2-(4-aminophenyl)ethyladenosine (APNEA), which when radiolabelled with 125I shows high affinity for the newly described adenosine A3 receptor, have been investigated in the angiotensin II-supported circulation of the pithed rat. APNEA induces hypotensive responses which are unaffected