2-Chloroadenosine structure
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Common Name | 2-Chloroadenosine | ||
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CAS Number | 146-77-0 | Molecular Weight | 301.686 | |
Density | 2.2±0.1 g/cm3 | Boiling Point | 643.3±65.0 °C at 760 mmHg | |
Molecular Formula | C10H12ClN5O4 | Melting Point | 162 °C | |
MSDS | Chinese USA | Flash Point | 342.8±34.3 °C |
Use of 2-Chloroadenosine2-Chloroadenosine, a stable adenosine analogue, protects against long term development of ischaemic cell loss in the rat hippocampus. 2-Chloroadenosine is an apparent competitive inhibitor of uridine influx (apparent Ki=33 μM) and high-affinity nitrobenzylthioinosine binding (apparent Ki=0.18 mM). 2-Chloroadenosine is a transported permeant for the nucleoside transporter in human erythrocytes[1][2]. |
Name | 2-Chloroadenosine |
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Synonym | More Synonyms |
Description | 2-Chloroadenosine, a stable adenosine analogue, protects against long term development of ischaemic cell loss in the rat hippocampus. 2-Chloroadenosine is an apparent competitive inhibitor of uridine influx (apparent Ki=33 μM) and high-affinity nitrobenzylthioinosine binding (apparent Ki=0.18 mM). 2-Chloroadenosine is a transported permeant for the nucleoside transporter in human erythrocytes[1][2]. |
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Related Catalog | |
References |
Density | 2.2±0.1 g/cm3 |
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Boiling Point | 643.3±65.0 °C at 760 mmHg |
Melting Point | 162 °C |
Molecular Formula | C10H12ClN5O4 |
Molecular Weight | 301.686 |
Flash Point | 342.8±34.3 °C |
Exact Mass | 301.057770 |
PSA | 139.54000 |
LogP | -0.46 |
Vapour Pressure | 0.0±2.0 mmHg at 25°C |
Index of Refraction | 1.912 |
Water Solubility | H2O: 10 mg/mL, clear, colorless |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | AU7357550 |
Precursor 7 | |
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DownStream 10 | |
Hypoxanthine uptake by skeletal muscle microvascular endothelial cells from equilibrative nucleoside transporter 1 (ENT1)-null mice: effect of oxidative stress.
Microvasc. Res. 98 , 16-22, (2015) Adenosine is an endogenous regulator of vascular tone. This activity of adenosine is terminated by its uptake and metabolism by microvascular endothelial cells (MVEC). The predominant transporter invo... |
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Oxidative stress modulates nucleobase transport in microvascular endothelial cells
Microvasc. Res. 95 , 68-75, (2014) Purine nucleosides and nucleobases play key roles in the physiological response to vascular ischemia/reperfusion events. The intra- and extracellular concentrations of these compounds are controlled, ... |
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Chemical genetics reveals a complex functional ground state of neural stem cells.
Nat. Chem. Biol. 3(5) , 268-273, (2007) The identification of self-renewing and multipotent neural stem cells (NSCs) in the mammalian brain holds promise for the treatment of neurological diseases and has yielded new insight into brain canc... |
6-Amino-2-chloro-9-(β-D-ribofuranosyl)purine Hydrate |
2-CADO,6-Amino-2-chloropurine riboside |
2-Chloroadenosine |
6-Amino-2-chloropurine Riboside Hydrate |
2-CADO Hydrate |
EINECS 205-678-3 |
(2R,3R,4S,5R)-2-(6-Amino-2-chloro-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydro-3,4-furandiol |
MFCD00005734 |
Adenosine, 2-chloro- |
2-Chlor-9-(β-D-ribofuranosyl)-9H-purin-6-amin |
6-Amino-2-Chloropurine Riboside |
2-chloro adenosine |