6-O-Methyl Guanosine

6-O-Methyl Guanosine Structure
CAS No.
7803-88-5
Chemical Name:
6-O-Methyl Guanosine
Synonyms
6-OMe-Gr;NSC 66381;Brn 0703603;O-Methylguanosine;o-methyl-guanosin;O6-METHYLGUANOSINE;6-O-METHYLGUANOSINE;6-Methoxy-guanosine;Guanosine, o-methyl-;Guanosine, 6-O-methyl-
CBNumber:
CB8290854
Molecular Formula:
C11H15N5O5
Molecular Weight:
297.27
MOL File:
7803-88-5.mol
MSDS File:
SDS
Modify Date:
2023/5/18 11:31:18

6-O-Methyl Guanosine Properties

Melting point 120 °C(Solv: ethyl ether (60-29-7); methanol (67-56-1))
Boiling point 721.0±70.0 °C(Predicted)
Density 1.98±0.1 g/cm3(Predicted)
storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility DMSO (Slightly), Methanol (Very Slightly), Water (Slightly)
form Solid
pka 13.07±0.70(Predicted)
color White to Pale Yellow
Water Solubility Water : 2 mg/mL (6.73 mM; Need ultrasonic and warming)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

6-O-Methyl Guanosine Chemical Properties,Uses,Production

Chemical Properties

White Solid

Uses

6-O-Methyl Guanosine is a guanine derivative that acts as modulators of GTPases and modulator-resistant enzymes; used in drug design and target validation

6-O-Methyl Guanosine Preparation Products And Raw materials

Raw materials

Preparation Products

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O6-METHYLGUANOSINE o-methoxydeoxyguanosine o-methyl-guanosin 6-O-METHYLGUANOSINE 2-Amino-6-methoxy-9-b-D-ribofuranosyl-9H-purine 2-Amino-6-methoxypurine Ribonucleoside 6-Methoxy-9-b-D-ribofuranosyl-9H-purin-2-amine NSC 66381 2-Amino-6-methoxy-9--D-ribofuranosyl-9H-purine 6-Methoxy-9--D-ribofuranosyl-9H-purin-2-amine O-Methylguanosine 6-Methoxy-6-deoxoguanosine 9-β-D-Ribofuranosyl-1,6-dihydro-6-methoxy-9H-purin-2-amine Brn 0703603 Guanosine, o-methyl- 6-Methoxy-guanosine Guanosine, 6-O-methyl- 6-OMe-Gr inhibit,6 O Methyl Guanosine,Nucleoside Antimetabolite/Analog,6OMethyl Guanosine,Inhibitor 7803-88-5 Bases & Related Reagents Carbohydrates & Derivatives Heterocycles Nucleotides