Cart
sales@molnova.com
2-Aminopurine-9-beta-D-(2’-deoxy)riboside
CAS No. 3616-24-8
2-Aminopurine-9-beta-D-(2’-deoxy)riboside( —— )
Catalog No. M37900 CAS No. 3616-24-8
2-Aminopurine-9-beta-D-(2’-deoxy)riboside, a derivative of 2-Aminopurine, is a modified nucleoside composed of a purine base linked to a (2’-deoxy)ribose sugar moiety.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 10MG | 29 | In Stock |
|
| 25MG | 51 | In Stock |
|
| 50MG | 75 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Name2-Aminopurine-9-beta-D-(2’-deoxy)riboside
-
NoteResearch use only, not for human use.
-
Brief Description2-Aminopurine-9-beta-D-(2’-deoxy)riboside, a derivative of 2-Aminopurine, is a modified nucleoside composed of a purine base linked to a (2’-deoxy)ribose sugar moiety.
-
Description2-Aminopurine-9-beta-D-(2’-deoxy)riboside, a derivative of 2-Aminopurine, is a modified nucleoside composed of a purine base linked to a (2’-deoxy)ribose sugar moiety.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number3616-24-8
-
Formula Weight251.24
-
Molecular FormulaC10H13N5O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESNC=1N=C2N(C=NC2=CN1)[C@@H]3O[C@H](CO)[C@@H](O)C3
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
Cimiracemoside D
Cimiracemoside D is a natural product from Cimicifuga foetida L.
-
6,7-Dimethoxy-2-[2-(...
NF-κB-IN-13 (compound 12) can significantly inhibit LPS-induced NF-κB activation and NO production in RAW264.7 macrophages. NF-κB-IN-13 has anti-inflammatory effects.
-
FA-alkyne
FA-alkyne (FA alkyne) is a fluorescein that is a competitive probe for natural S-succinylation in FH-/- and FH+/+ cells and can be used to synthesize nanophotosensors.
