Cart
sales@molnova.com
Fludrocortisone acetate
CAS No. 514-36-3
Fludrocortisone acetate( 9α-fluoro Hydrocortisone Acetate | NSC 15186 | U 4845 )
Catalog No. M14781 CAS No. 514-36-3
Fludrocortisone Acetate is a synthetic mineralocorticoid, used to control the amount of sodium and fluids in your body.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
|
| 100MG | 27 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameFludrocortisone acetate
-
NoteResearch use only, not for human use.
-
Brief DescriptionFludrocortisone Acetate is a synthetic mineralocorticoid, used to control the amount of sodium and fluids in your body.
-
DescriptionFludrocortisone Acetate is a synthetic mineralocorticoid, used to control the amount of sodium and fluids in your body. It is used to treat Addison's disease by decreasing the amount of sodium that is lost (excreted) in your urine,also used to increase blood pressure.
-
In Vitro——
-
In Vivo——
-
Synonyms9α-fluoro Hydrocortisone Acetate | NSC 15186 | U 4845
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research AreaInflammation/Immunology
-
Indication——
Chemical Information
-
CAS Number514-36-3
-
Formula Weight422.5
-
Molecular FormulaC23H31FO6
-
Purity>98% (HPLC)
-
SolubilityDMSO: 10 mM
-
SMILESCC(=O)OCC(=O)[C@]1(CC[C@@H]2[C@@]1(C[C@@H]([C@]3([C@H]2CCC4=CC(=O)CC[C@@]43C)F)O)C)O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
(2S,3S)-3-Hydroxy-2-...
(2S,3S)-3-Hydroxy-2-methyl-3-phenylpropanoic acid is a chemical synthesis intermediate.
-
PNU-282987
PNU-282987 is a potent α7 nicotinic acetylcholine receptor (nAChR) agonist with an EC50 of 154 nM. PNU-282987 is also a functional antagonist of the 5-HT3 receptor with an IC50 of 4541 nM. PNU-282987 can be used for the research of central and peripheral nervous systems.
-
PF-543
PF-543, a novel sphingosine-competitive inhibitor of SphK1, inhibits SphK1 with IC50 and Ki of 2.0 nM and 3.6 nM.
