D1285
2′,3′-脱氧腺苷
≥97% (HPLC)
别名:
Dideoxyadenosine, ddA
并加购，请在购物车里查看协议价、货期和发货地。
选择规格
变更视图
关于此项目
经验公式（希尔记法）:
C10H13N5O2
化学文摘社编号:
分子量:
235.24
UNSPSC Code:
41106305
NACRES:
NA.51
PubChem Substance ID:
EC Number:
223-853-2
Beilstein/REAXYS Number:
619924
MDL number:
Assay:
≥97% (HPLC)
Form:
powder
Solubility:
water: 100 mg/mL, clear, colorless
Storage temp.:
2-8°C
Quality Segment
assay
≥97% (HPLC)
form
powder
optical activity
[α]/D -28.0±1.0
mp
181-184 °C (lit.)
solubility
water: 100 mg/mL, clear, colorless
storage temp.
2-8°C
SMILES string
Nc1ncnc2n(cnc12)[C@H]3CC[C@@H](CO)O3
InChI
1S/C10H13N5O2/c11-9-8-10(13-4-12-9)15(5-14-8)7-2-1-6(3-16)17-7/h4-7,16H,1-3H2,(H2,11,12,13)/t6-,7+/m0/s1
InChI key
WVXRAFOPTSTNLL-NKWVEPMBSA-N
Gene Information
human ... DCK(1633)
General description
2′,3′-Dideoxyadenosine is a nucleoside analog of deoxyadenosine. On deamination, it is converted to dideoxyinosine. It inhibits adenylyl cyclase and may play a key role in the inhibition of tumor progression. It is a potent inhibitor of reverse transcriptase enzyme of human immunodeficiency virus.
Application
2′,3′-Dideoxyadenosine (ddA), a specific adenylyl cyclase inhibitor, is useful in biological process and pathway studies involving adenylyl cyclase activity and cAMP pool modulation.
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)