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HCID 102213Erstellt: 3. November 2026

2'-O-Methyladenosine

AMI · (2R,3R,4R,5R)-5-(6-AMino-9H-purin-9-yl)-2-(hydroxyMethyl)-4-Methoxytetrahydrofuran-3-ol · 2'-OMe-A · OMe-rA · cordysinin B · 2’-0MeA · 2'-OMe A · 2'-OMe-rA

https://huagongshe.com/de/chemical/102213

Molekülstruktur von 2'-O-Methyladenosine

Identifikatoren & physikalische Daten

CAS No.2140-79-6
SummenformelC11H15N5O4
Durchschnittliche Molmasse281,272 g/mol
Monoisotopische Masse281,11240396 g/mol
SMILESCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(N)ncnc21
InChIKeyFPUGCISOLXNPPC-IOSLPCCCSA-N
PubChem CID102213
ChEMBLCHEMBL73237
ChEBICHEBI:69426
DTXSIDDTXSID50175671

Chemische & physikalische Eigenschaften

Schmelzpunkt200-202 C
Siedepunkt623.8±65.0 °C(Predicted)
Dichte1.84±0.1 g/cm3(Predicted)
LagerbedingungenKeep in dark place,Inert atmosphere,Store in freezer, under -20°C
LöslichkeitDMSO (Slightly), Methanol (Slightly, Heated, Sonicated), Water (Slightly)Soluble in water.
AggregatzustandPowder
pKa (Säurekonstante)13.13±0.70(Predicted)
FarbeWhite to Off-white
InChIInChI=1S/C11H15N5O4/c1-19-8-7(18)5(2-17)20-11(8)16-4-15-6-9(12)13-3-14-10(6)16/h3-5,7-8,11,17-18H,2H2,1H3,(H2,12,13,14)/t5-,7-,8-,11-/m1/s1
InChIKeyFPUGCISOLXNPPC-YGHVBYMHSA-N
SMILESOC[C@H]1O[C@@H](N2C3C(=C(N=CN=3)N)N=C2)[C@H](OC)[C@@H]1O
CAS Datenbank2140-79-6(CAS DataBase Reference)

Sicherheit & Vorschriften

Wassergefährdungsklasse (WGK)3
Zollcode29349990
R-Sätze (R)36/37/38
GefahrensymboleXi
Sicherheitshinweise (S)26-36-24/25

Anwendungen & Verwendung

Beschreibung

2'-O-Methyladenosine (Cordysinin B) is a member of the class of adenosines that is adenosine in which the hydroxy group at position 2' is replaced by a methoxy group. It has been isolated from the mycelia of Cordyceps sinensis. It has a role as a fungal metabolite. It is a member of adenosines and an ether. It derives from an adenosine. analogue with antiviral properties, starting material for 2'-O'-methyl nucleotides. Potential metabolite of 2'-O-Me-cAMP.

Verwenden

2'-O-Methyladenosine is an analog of adenosine used to prepare nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase.