Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Biochemical Engineering >  Plant extracts >  2-HYDROXYADENOSINE

2-HYDROXYADENOSINE

Basic information Safety Supplier Related

2-HYDROXYADENOSINE Basic information

Product Name:
2-HYDROXYADENOSINE
Synonyms:
  • Adenosine, 2,3-dihydro-2-oxo-
  • Regadenoson Impurity 17
  • 6-amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3,9-dihydro-2H-purin-2-one
  • Crotonoside, 98%, from Croton tiglium L.
  • Adenosine Impurity 6
  • 1,2-dihydro-2-oxo-adenosin
  • 1,2-dihydro-2-oxoadenosine
  • 6-amino-9-beta-d-ribofuranosyl-9h-purin-2-o
CAS:
1818-71-9
MF:
C10H13N5O5
MW:
283.24
Product Categories:
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
Mol File:
1818-71-9.mol
More
Less

2-HYDROXYADENOSINE Chemical Properties

storage temp. 
-20°C
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
powder
Density 
2.25±0.1 g/cm3(Predicted)
Melting point:
237-241 °C(Solv: water (7732-18-5))
pka
8.25±0.40(Predicted)
color 
White to off-white
More
Less

Safety Information

Safety Statements 
24/25
WGK Germany 
3
HS Code 
29349990
More
Less

2-HYDROXYADENOSINE Usage And Synthesis

Description

Crotonoside is a purine analogue that is structurally similar to pyrazole, which also inhibits the polymerase chain reaction in vitro. Crotonoside has been shown to be an inhibitor of the polymerase chain reaction in vitro, but it is unclear if this activity will translate to in vivo models.

Chemical Properties

White crystals, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from the fruit of Croton tiglium L.

Uses

2-?Hydroxyadenosine is an isoquinoline alkaloid displaying anticancer activity.

Definition

ChEBI: Crotonoside is a purine nucleoside.

in vivo

Crotonoside(intraperitoneal and intravenous injection; 70 mg/kg, 35 mg/kg; once daily) induces a significant antitumor activity and inhibited xenograft tumor progress as compared to treatment with vehicle[1].

Animal Model: NOD-SCID mice with MV4-11 cells[1]
Dosage:70 mg/kg, 35 mg/kg
Administration:Intraperitoneal and intravenous injection; 70 mg/kg, 35 mg/kg; once daily
Result:Produced significant AML tumor inhibition rates of 93.5% at 70 mg/kg.

target

Adenosine Receptor

IC 50

FLT3; HDAC3; HDAC6

2-HYDROXYADENOSINESupplier

Hongene Biotech Corporation
Tel
021-64757213
Email
info@hongene.com
Chembest Research Laboratories Limited
Tel
+86-21-20908456
Email
sales@BioChemBest.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Email
cdhxsj@163.com
Shenzhen Sungening Bio-Tech Co., Ltd
Tel
+86-0755-89668383
Email
sales@sungening.com