2'-Deoxyadenosine


CAS No. : 958-09-8

958-09-8
Price and Availability of CAS No. : 958-09-8
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Cat. No. : HY-W040329
M.Wt: 251.25
Formula: C10H13N5O3
Purity: >98 %
Solubility: DMSO : 100 mg/mL (ultrasonic);H2O : 16.67 mg/mL (ultrasonic)
Introduction of 958-09-8 :

2′-Deoxyadenosine is an adenine nucleoside that inhibits glucose-stimulated insulin release. 2′-Deoxyadenosine inhibits glucose-stimulated increases seen in islet cyclic AMP (cAMP) accumulation. 2'-Deoxyadenosine activates caspase-3 and promotes apoptosis. 2'-Deoxyadenosine inhibits the activity of S-adenosyl-L-homocysteine hydrolase (SAHH). 2'-Deoxyadenosine inhibits the growth of various cells. 2'-Deoxyadenosine has an anticancer effect on colon cancer[1][2][3]. In Vitro:2'-Deoxyadenosine (10 mM) does not inhibit insulin biosynthesis or [U-14C]glucose oxidation at concentrations of the nucleosides that gave maximal inhibition of insulin release. 2'-Deoxyadenosine monohydrate produces marked inhibition of the glucose-stimulated increases seen in islet cyclic AMP accumulation[1].
2'-Deoxyadenosine (0.01-0.5 mM; 24-72 h) inhibits the growth of LoVo human colon carcinoma cells in a concentration- and time-dependent manner and promotes apoptosis, as indicated by characteristic apoptotic morphology[2].
2'-Deoxyadenosine inhibits S-adenosyl-L-homocysteine hydrolase activity in crude extracts of L1210 leukemia cells in a time-dependent manner when assays are conducted in the presence of Deoxycoformycin (HY-A0006)[3].
2'-Deoxyadenosine (0.1-2 mM; up to 3 h) inhibits pig keratinocyte outgrowth, [3H] thymidine uptake, and mitosis[4].
2'-Deoxyadenosine (0.1 mM; 4 days) in combination with 1 μM dCF inhibits the growth of LoVo cells in a cell-density-dependent manner[5].
2'-Deoxyadenosine (100 μM; 3 days) in the presence of 3 μM Deoxycoformycin (HY-A0006) is toxic to rat chromaffin cells, causing apoptosis-like cell death, as shown by morphological changes, DNA fragmentation, and increased dATP levels[6].
2'-Deoxyadenosine (0.1 mM) in the presence of 0.01 mM dCF in vitro leads to a significant increase in dATP levels in mouse embryos[7].

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