Size | Price | Stock | Qty |
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50mg |
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100mg |
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250mg |
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500mg |
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1g |
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Other Sizes |
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Purity: ≥98%
Corticosterone is an adrenocortical steroid and also an endogenous steroid hormone involved in immune responses, stress responses and energy homeostasis. It activates mineralocorticoid and glucocorticoid receptors.
ln Vitro |
Corticosterone (100 nM; 30 minutes) phosphorylates GDI Ser-213 via SGK, enhances the GDI-Rab4 complex's formation, and encourages Rab4's functional recycling as well as Rab4-mediated AMPAR recycling to the synaptic membrane [1]. Good immunosuppressive characteristics are shown by corticosterone (CORT) (1 µM; 48 hours), which functionally inhibits BMDC maturation and hence inhibits LPS-induced maturation-related markers (MHC class II, B7.2, B7.1, and CD40) [2].
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ln Vivo |
Corticosterone significantly impairs BMDC cells' capacity to stimulate naive CD8+ T cells in vivo [2]. In the dentate gyrus and CA1 of rats, corticosterone (0.03 or 1 mg/kg; subcutaneous; single dosage) suppresses the expression of BDNF mRNA [3]. In adrenalectomized (ADX) rats, corticosterone (2.6 mg/kg; in animal feed; 8 days) returns ethanol intake and preference to about preoperative levels [4].
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Cell Assay |
Cell viability assay [2]
Cell Types: BMDC Cell Tested Concentrations: 1 µM Incubation Duration: 48 h Experimental Results: Completely blocked LPS-induced expression of MHC class II and B7.2, and maximally damaged BMDC cells at 12 h Mature. B7.1 diminished by 50%, and CD40 was slightly downregulated. |
Animal Protocol |
Animal/Disease Models: Adult male Wistar rat (150-170 g; adrenalectomy) [3].
Doses: 0.03 or 1 mg/kg Route of Administration: subcutaneous injection; single. Experimental Results: The expression of BDNF mRNA in the dentate gyrus diminished by 25% and 50% at doses of 0.03 and 1 mg/kg (3 hrs (hrs (hours)) after administration). Compared with the control group at t=0 hrs (hrs (hours)) (3 hrs (hrs (hours)) after administration), BDNF mRNA levels diminished by approximately 40%, but levels increased by 100% at 12 hrs (hrs (hours)) after administration (compared with the t=3 hrs (hrs (hours)) and t=6 hrs (hrs (hours)) groups ). Animal/Disease Models: Male Wistar rat (3 weeks old; adrenalectomy) [4]. Doses: 2.6 mg/kg Route of Administration: Animal feed; 8 days. Experimental Results: Ethanol intake and preference in adrenalectomized (ADX) rats returned to approximately normal preoperative levels and to levels observed in sham-operated (SH) rats. |
References |
[1]. Elftman MD, et al. Corticosterone impairs dendritic cell maturation and function. Immunology. 2007 Oct;122(2):279-90.
[2]. Schaaf MJ, et al. Downregulation of BDNF mRNA and protein in the rat hippocampus by corticosterone. Brain Res. 1998 Nov 30;813(1):112-20. [3]. Fahlke C, et al. Involvement of corticosterone in the modulation of ethanol consumption in the rat. Alcohol. 1994 May-Jun;11(3):195-202. |
Molecular Formula |
C21H30O4
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Molecular Weight |
346.4605
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CAS # |
50-22-6
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Related CAS # |
Corticosterone-d8;1271728-07-4;Corticosterone-d4;2243253-91-8
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SMILES |
C[C@@]12[C@@H](C(CO)=O)CC[C@@]1([H])[C@]3([H])CCC4=CC(CC[C@]4(C)[C@@]3([H])[C@@H](O)C2)=O
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InChi Key |
OMFXVFTZEKFJBZ-HJTSIMOOSA-N
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InChi Code |
InChI=1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3/t14-,15-,16+,17-,19+,20-,21-/m0/s1
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Chemical Name |
(8S,9S,10R,11S,13S,14S,17S)-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3H-cyclopenta[a]phenanthren-3-one
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Synonyms |
BRN 2339601 BRN-233960 BRN233960 CCRIS 6753 CCRIS-6753 CCRIS6753 NSC 9705 NSC-9705 NSC9705
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Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
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Solubility (In Vitro) |
DMSO : ~100 mg/mL (~288.63 mM)
Ethanol : ~14.29 mg/mL (~41.25 mM) H2O : ~0.67 mg/mL (~1.93 mM) |
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Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 2.5 mg/mL (7.22 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 2: ≥ 2.5 mg/mL (7.22 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly. Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution. View More
Solubility in Formulation 3: ≥ 2.5 mg/mL (7.22 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution. Solubility in Formulation 4: ≥ 1.43 mg/mL (4.13 mM) (saturation unknown) in 10% EtOH + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 14.3 mg/mL clear EtOH stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 5: ≥ 1.43 mg/mL (4.13 mM) (saturation unknown) in 10% EtOH + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 14.3 mg/mL clear EtOH stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly. Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution. Solubility in Formulation 6: ≥ 1.43 mg/mL (4.13 mM) (saturation unknown) in 10% EtOH + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution. For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 14.3 mg/mL clear EtOH stock solution to 900 μL of corn oil and mix well. Solubility in Formulation 7: 2 mg/mL (5.77 mM) in 0.5% CMC-Na/saline water (add these co-solvents sequentially from left to right, and one by one), suspension solution; with ultrasonication (<60°C). Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 8: 4 mg/mL (11.55 mM) in 20% HP-β-CD in Saline (add these co-solvents sequentially from left to right, and one by one), suspension solution; with ultrasonication. Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution. Solubility in Formulation 9: 5 mg/mL (14.43 mM) in 5% Cremophor EL 95% (20% HP-β-CD) (add these co-solvents sequentially from left to right, and one by one), clear solution; with ultrasonication. |
Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
1 mM | 2.8863 mL | 14.4317 mL | 28.8634 mL | |
5 mM | 0.5773 mL | 2.8863 mL | 5.7727 mL | |
10 mM | 0.2886 mL | 1.4432 mL | 2.8863 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration: mg/mL;
Method for preparing DMSO stock solution: mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation::Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O,mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.