CAS 120225-75-4
:1-(6-Amino-2-cloro-9H-purina-9-il)-1-desoxi-N-etil-2,3-O-(1-metiletilideno)-β-D-ribofuranuronamida
Fórmula:C15H19ClN6O4
InChI:InChI=1S/C15H19ClN6O4/c1-4-18-12(23)8-7-9(26-15(2,3)25-7)13(24-8)22-5-19-6-10(17)20-14(16)21-11(6)22/h5,7-9,13H,4H2,1-3H3,(H,18,23)(H2,17,20,21)/t7-,8+,9-,13-/m1/s1
Clave InChI:InChIKey=CHPHKXXDQSHQKC-LOKDSWTASA-N
SMILES:C(NCC)(=O)[C@H]1O[C@H]([C@]2([C@@]1(OC(C)(C)O2)[H])[H])N3C=4C(N=C3)=C(N)N=C(Cl)N4
Sinónimos:- 1-(6-Amino-2-chloro-9H-purin-9-yl)-1-deoxy-N-ethyl-2,3-O-(1-methylethylidene)-β-<span class="text-smallcaps">D</span>-ribofuranuronamide
- 2-Chloro-23O-isopropylideneadenosine-5N-ethylcaboxamide
- Furo[3,4-d]-1,3-dioxole, β-<span class="text-smallcaps">D</span>-ribofuranuronamide deriv.
- β-<span class="text-smallcaps">D</span>-Ribofuranuronamide, 1-(6-amino-2-chloro-9H-purin-9-yl)-1-deoxy-N-ethyl-2,3-O-(1-methylethylidene)-
- Furo[3,4-d]-1,3-dioxole, β-D-ribofuranuronamide deriv.
- 1-(6-Amino-2-chloro-9H-purin-9-yl)-1-deoxy-N-ethyl-2,3-O-(1-methylethylidene)-β-D-ribofuranuronamide
- β-D-Ribofuranuronamide, 1-(6-amino-2-chloro-9H-purin-9-yl)-1-deoxy-N-ethyl-2,3-O-(1-methylethylidene)-
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2-Chloro-2’,3’-O-isopropylideneadenosine-5’-N-ethylcarboxamide
CAS:Producto controladoApplications 2-Chloro-2’,3’-O-isopropylideneadenosine-5’-N-ethylcarboxamide is a potent and selective adenosine receptor agonist (1). It is also used to prepare photoreactive 2-phenethylamine derivatives (2).
References (1) Hutchison, A.J., et al.: J. Med. Chem., 33, 1919 (1990)(2) Murai, Y., et al.: Eur. J. Org. Chem 2013, 2428 (2013)Fórmula:C15H19ClN6O4Forma y color:NeatPeso molecular:382.82-Chloro-5'-N-ethylcarboxamide-2',3'-O-isopropylidene adenosine
CAS:2-Chloro-5'-N-ethylcarboxamide-2',3'-O-isopropylidene adenosine is an antiviral agent that inhibits the synthesis of deoxyribonucleic acid (DNA) and ribonucleic acid (RNA). It is a synthetic, modified nucleoside. 2-Chloro-5'-N-ethylcarboxamide-2',3'-O-isopropylidene adenosine has been shown to be active against human tumor cell lines in vitro and in vivo. The compound inhibits the activity of DNA polymerase and RNA polymerase by competitive inhibition of the enzyme phosphoramidite. 2CECA has also been shown to have anticancer properties as it induces apoptosis in cancer cells.Fórmula:C15H19ClN6O4Pureza:Min. 95%Peso molecular:382.8 g/molRef: 3D-NC16518
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