Cart
sales@molnova.com
SR4554
CAS No. 167648-73-9
SR4554( —— )
Catalog No. M34714 CAS No. 167648-73-9
SR4554 is a fluorinated 2-nitroimidazole non-invasive tumor hypoxia probe for the detection of tumor hypoxia as detected by 19F magnetic resonance spectroscopy (MRS).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 445 | Get Quote |
|
| 5MG | 686 | Get Quote |
|
| 10MG | 938 | Get Quote |
|
| 25MG | 1398 | Get Quote |
|
| 50MG | 1822 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameSR4554
-
NoteResearch use only, not for human use.
-
Brief DescriptionSR4554 is a fluorinated 2-nitroimidazole non-invasive tumor hypoxia probe for the detection of tumor hypoxia as detected by 19F magnetic resonance spectroscopy (MRS).
-
DescriptionSR4554 is a fluorinated 2-nitroimidazole non-invasive tumor hypoxia probe for the detection of tumor hypoxia as detected by 19F magnetic resonance spectroscopy (MRS).
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number167648-73-9
-
Formula Weight282.18
-
Molecular FormulaC8H9F3N4O4
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C(NCC(O)C(F)(F)F)CN1C=CN=C1N(=O)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
FG 7142
FG 7142?also modulates GABA-induced chloride flux at GABAA receptors expressing the α1 subunit (EC50= 137 nM).?FG 7142?can increase tyrosine hydroxylation and cause upregulation of β-adrenoceptors in mouse cerebral cortex.?FG 7142 , a non-selectively benzodiazepine inverse agonist, has high affinity for the α1 subunit-containing GABAA receptor (Ki=91 nM).?
-
Peptide F, bovine
Peptide F, bovine
-
Ethylenebis(oxyethyl...
Ethylene glycol?bis(2-aminoethyl)tetraacetic acid is a diether that is?ethylene glycol?in which the hydrogens of the?hydroxy?groups have been replaced by 2-[bis(carboxymethyl)amino]ethyl group respectively.
