Medroxyprogesterone acetate
Based on 35 publication(s) in Google Scholar
Medroxyprogesterone acetate is a widely used synthetic steroid by its interaction with progesterone, androgen and glucocorticoid receptors.
For research use only. We do not sell to patients.
- Purity: 99.88%
- CAS No.: 71-58-9
- Formula: C24H34O4
- Molecular Weight:386.52
-
Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 1 year , -20°C, 6 months
Publications Citing Use of MedChemExpress (MCE) Medroxyprogesterone acetate
More- Signal Transduct Target Ther. 2023 May 10;8(1):183. [Abstract]
- Nat Commun. 2024 Oct 8;15(1):8708. [Abstract]
- J Adv Res. 2026 Feb 19:S2090-1232(26)00162-1. [Abstract]
- Redox Biol. 2025 Jun:83:103615. [Abstract]
- Adv Sci (Weinh). 2026 Mar 12:e20455. [Abstract]
- Oncogene. 2025 Sep 13. [Abstract]
- EMBO J. 2024 Nov;43(21):5018-5036. [Abstract]
- Mol Med. 2024 Sep 12;30(1):147. [Abstract]
- Hum Reprod. 2024 May 23:deae111. [Abstract]
- Biochem Pharmacol. 2025 Jun 23:117060. [Abstract]
- Reprod Biol Endocrinol. 2022 Sep 22;20(1):142. [Abstract]
- Int J Mol Sci. 2023 Mar 7;24(6):5111. [Abstract]
- Toxicology. 2025 Jan 29:154069. [Abstract]
- Biochim Biophys Acta Mol Basis Dis. 2025 Jan;1871(1):167526. [Abstract]
- Virol Sin. 2026 Jan 23:S1995-820X(26)00008-8. [Abstract]
- Cell Signal. 2024 Dec:124:111438. [Abstract]
- Genes Immun. 2026 Mar 10. [Abstract]
- FEBS J. 2025 Jul 25. [Abstract]
- Curr Issues Mol Biol. 2024 Apr 19;46(4):3579-3594. [Abstract]
- Reprod Biomed Online. 2023 Feb;46(2):225-233. [Abstract]
- Vet Res. 2026 Jun 9;57(1):102. [Abstract]
- Endocrinology. 2024 Apr 29;165(6):bqae049. [Abstract]
- Arch Biochem Biophys. 2025 Oct:772:110552. [Abstract]
- J Reprod Immunol. 2023 Feb:155:103788. [Abstract]
- J Reprod Immunol. 2022 Jun;151:103623. [Abstract]
- Mol Cell Endocrinol. 2025 May 19:112581. [Abstract]
- Mol Cell Endocrinol. 2023 Aug 20:574:111952. [Abstract]
- J Proteomics. 2025 Apr 3:316:105437. [Abstract]
- J Assist Reprod Genet. 2024 Jun;41(6):1669-1685. [Abstract]
- Mol Reprod Dev. 2025 May;92(5):e70025. [Abstract]
- Res Sq. 2025 Jul 14.
- bioRxiv. 2024 Feb 8.
- SSRN. 2023 Aug 1.
- Research Square Preprint. 2022 Jan.
- Patent. US20200078369A1
-
WB
-
In Vivo Efficacy Study
-
Apoptosis Analysis
-
IF
-
Cell Proliferation/Viability Assay
All Endogenous Metabolite Isoforms
More
Biological Activity
|
Human Endogenous Metabolite |
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | EC50 |
10 nM
Compound: 2 (MPA)
|
Effective concentration against glucocorticoid receptor in human lung A549 cells
Effective concentration against glucocorticoid receptor in human lung A549 cells
|
[PMID: 12657272] |
| AN3-CA | IC50 |
37.1 μM
Compound: MPA
|
Antiproliferative activity against human AN3CA cells assessed as inhibition of cell viability by CCK8 assay
Antiproliferative activity against human AN3CA cells assessed as inhibition of cell viability by CCK8 assay
|
[PMID: 32527541] |
| CV-1 | EC50 |
0.15 nM
Compound: MPA
|
Compound was tested for agonistic activity by cotransfection assay against human Progesterone receptor in CV-1 cells
Compound was tested for agonistic activity by cotransfection assay against human Progesterone receptor in CV-1 cells
|
[PMID: 10212133] |
| CV-1 | EC50 |
0.15 nM
Compound: 3 (MPA)
|
Agonistic activity against human progesterone receptor expressed in CV-1 cells
Agonistic activity against human progesterone receptor expressed in CV-1 cells
|
[PMID: 12954062] |
| CV-1 | EC50 |
0.15 nM
Compound: MPA
|
Agonistic activity to the human progesterone receptor (hPR)assayed in CV-1 cells in cotransfection assay.
Agonistic activity to the human progesterone receptor (hPR)assayed in CV-1 cells in cotransfection assay.
|
[PMID: 9464360] |
| CV-1 | EC50 |
10 nM
Compound: MPA
|
Agonist activity against Human glucocorticoid receptor(hGR) expressed in CV-1 cells
Agonist activity against Human glucocorticoid receptor(hGR) expressed in CV-1 cells
|
[PMID: 9464360] |
| CV-1 | EC50 |
6.1 nM
Compound: MPA
|
Agonistic activity against Human androgen receptor(hAR) expressed in CV-1 cells
Agonistic activity against Human androgen receptor(hAR) expressed in CV-1 cells
|
[PMID: 9464360] |
| CV-1 | EC50 |
924 nM
Compound: MPA
|
Agonistic activity against Human estrogen receptor(hER) expressed in CV-1 cells
Agonistic activity against Human estrogen receptor(hER) expressed in CV-1 cells
|
[PMID: 9464360] |
| CV-1 | IC50 |
1197 nM
Compound: MPA
|
Antagonistic activity was determined in Human mineralocorticoid receptor(hMR) of CV-1 cells in cotransfection assay.
Antagonistic activity was determined in Human mineralocorticoid receptor(hMR) of CV-1 cells in cotransfection assay.
|
[PMID: 9464360] |
| CV-1 | IC50 |
<10000 nM
Compound: MPA
|
Antagonistic activity was determined in Human progesterone receptor(hPR) of CV-1 cells in cotransfection assay.
Antagonistic activity was determined in Human progesterone receptor(hPR) of CV-1 cells in cotransfection assay.
|
[PMID: 9464360] |
| CV-1 | EC50 |
0.15 nM
Compound: MPA
|
Agonistic activity was measured for modulation of hPR-B (human progesterone receptor) in co-transfected CV-1 cells.
Agonistic activity was measured for modulation of hPR-B (human progesterone receptor) in co-transfected CV-1 cells.
|
[PMID: 9464361] |
| CV-1 | EC50 |
0.15 nM
Compound: MPA
|
Effective concentration (EC50) against human progesterone receptor expressed in CV-1 cell
Effective concentration (EC50) against human progesterone receptor expressed in CV-1 cell
|
[PMID: 9784110] |
| CV-1 | IC50 |
10 nM
Compound: MPA
|
Inhibitory activity (IC50) against human glucocorticoid receptor expressed in CV-1 cells
Inhibitory activity (IC50) against human glucocorticoid receptor expressed in CV-1 cells
|
[PMID: 9784110] |
| CV-1 | IC50 |
1197 nM
Compound: MPA
|
Inhibitory activity (IC50) against human mineralocorticoid receptor expressed in CV-1 cells
Inhibitory activity (IC50) against human mineralocorticoid receptor expressed in CV-1 cells
|
[PMID: 9784110] |
| CV-1 | IC50 |
6.1 nM
Compound: MPA
|
Inhibitory activity (IC50) against human androgen receptor expressed in CV-1 cells
Inhibitory activity (IC50) against human androgen receptor expressed in CV-1 cells
|
[PMID: 9784110] |
| CV-1 | IC50 |
924 nM
Compound: MPA
|
IC50 determined against human estrogen receptor in CV-1 cells
IC50 determined against human estrogen receptor in CV-1 cells
|
[PMID: 9784110] |
| HEC-1-A | IC50 |
51.8 μM
Compound: MPA
|
Antiproliferative activity against human Hec1A cells assessed as inhibition of cell viability by CCK8 assay
Antiproliferative activity against human Hec1A cells assessed as inhibition of cell viability by CCK8 assay
|
[PMID: 32527541] |
| HEC-1B cell line | IC50 |
60.4 μM
Compound: MPA
|
Antiproliferative activity against human HEC1B cells assessed as inhibition of cell viability by CCK8 assay
Antiproliferative activity against human HEC1B cells assessed as inhibition of cell viability by CCK8 assay
|
[PMID: 32527541] |
| Ishikawa | IC50 |
37 μM
Compound: MPA
|
Antiproliferative activity against human Ishikawa cells assessed as inhibition of cell viability by CCK8 assay
Antiproliferative activity against human Ishikawa cells assessed as inhibition of cell viability by CCK8 assay
|
[PMID: 32527541] |
| KLE | IC50 |
>80 μM
Compound: MPA
|
Antiproliferative activity against human KLE cells assessed as inhibition of cell viability by CCK8 assay
Antiproliferative activity against human KLE cells assessed as inhibition of cell viability by CCK8 assay
|
[PMID: 32527541] |
| L929 | EC50 |
6.1 nM
Compound: 2 (MPA)
|
Effective concentration against Androgen receptor in mouse fibroblast L929 cells
Effective concentration against Androgen receptor in mouse fibroblast L929 cells
|
[PMID: 12657272] |
| T47D | EC50 |
0.33 nM
Compound: MPA
|
Agonistic activity by cotransfection assay against human Progesterone receptor in T47D cells
Agonistic activity by cotransfection assay against human Progesterone receptor in T47D cells
|
[PMID: 10212133] |
| T47D | EC50 |
0.12 nM
Compound: MPA
|
Agonistic activity against progesterone receptor in alkaline phosphatase assay using human T47D breast carcinoma cell line
Agonistic activity against progesterone receptor in alkaline phosphatase assay using human T47D breast carcinoma cell line
|
[PMID: 11859003] |
| T47D | IC50 |
10.8 nM
Compound: MPA
|
Binding affinity for Progesterone receptor (PR) in human T47D breast carcinoma cells
Binding affinity for Progesterone receptor (PR) in human T47D breast carcinoma cells
|
[PMID: 11859003] |
| T47D | EC50 |
0.1 nM
Compound: MPA (Medroxyprogesterone)
|
Effective concentration on alkaline phosphatase activity in human T47D breast carcinoma cell line.
Effective concentration on alkaline phosphatase activity in human T47D breast carcinoma cell line.
|
[PMID: 12657271] |
| T47D | IC50 |
10.8 nM
Compound: MPA (Medroxyprogesterone)
|
Inhibition of [3H]P4 to progesterone receptor (PR) of human T47D breast carcinoma cells
Inhibition of [3H]P4 to progesterone receptor (PR) of human T47D breast carcinoma cells
|
[PMID: 12657271] |
| T47D | EC50 |
0.5 nM
Compound: 2 (MPA)
|
Effective concentration of progesterone receptor agonist induction of alkaline phosphatase activity in human T47D breast carcinoma cells
Effective concentration of progesterone receptor agonist induction of alkaline phosphatase activity in human T47D breast carcinoma cells
|
[PMID: 12657272] |
| T47D | IC50 |
10.8 nM
Compound: 2 (MPA)
|
Inhibition of 3 nM [3H]R5020 binding to progesterone receptor in human T47D cells
Inhibition of 3 nM [3H]R5020 binding to progesterone receptor in human T47D cells
|
[PMID: 12657272] |
| T47D | EC50 |
0.33 nM
Compound: 3 (MPA)
|
Agonistic activity against human progesterone receptor in T47D breast cancer cells
Agonistic activity against human progesterone receptor in T47D breast cancer cells
|
[PMID: 12954062] |
| T47D | EC50 |
0.5 nM
Compound: MPA
|
Agonistic activity measures the ability to induce alkaline phosphatase in T47D human breast cancer cell line
Agonistic activity measures the ability to induce alkaline phosphatase in T47D human breast cancer cell line
|
[PMID: 15081005] |
| T47D | EC50 |
0.4 nM
Compound: MPA
|
Agonist activity at human progesterone receptor in human T47D cells assessed as alkaline phosphatase activity
Agonist activity at human progesterone receptor in human T47D cells assessed as alkaline phosphatase activity
|
[PMID: 18553958] |
Medroxyprogesterone acetate (10 and 0.5 nM, 48 h) inhibits Steroid-deprived HUVEC eNOS expression[2].
Medroxyprogesterone acetate (10 and 0.5 nM, 16 h) inhibits leukocyte adhesion to human endothelial cells (Steroid-deprived HUVECs) by reduing endothelial adhesion molecule (VCAM-1 and ICAM-1 protein) expression[2].
Medroxyprogesterone acetate (10 and 0.5 nM, 2 h) reduces NF-κB nuclear translocation in Steroid-deprived HUVECs[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:100 ng/ml LPS treated endothelial cells
-
Concentration:10 and 0.5 nM
-
Incubation Time:2h
-
Result:Inhibited NF-κB nuclear translocation.
Medroxyprogesterone acetate (0.05-0.2 mg/kg/day, p.o., 14 days, rats) increases allopregnanolone levels in all tissues except in the adrenal gland, and affects β-END levels in the hippocampus[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 71-58-9
-
Appearance Solid
-
Molecular Weight 386.52
-
Formula C24H34O4
-
Color White to off-white
-
SMILES
CC(O[C@@]([C@]12C)(CC[C@@]1([H])[C@@](C[C@H](C)C3=CC4=O)([H])[C@]([C@]3(CC4)C)([H])CC2)C(C)=O)=O
-
Synonyms
Medroxyprogesterone 17-acetate; Farlutin
-
Structure Classification
-
Initial Source
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 1 year -20°C 6 months
Publications (35)
-
Journal Impact Factor
-
Most Recent
-
Signal Transduct Target Ther
2023 May 10;8(1):183. PMID: 37160887
Medroxyprogesterone acetate purchased from MedChemExpress. Usage Cited in: Signal Transduct Target Ther. 2023 May 10;8(1):183. [Abstract]
Cisplatin-resistant OVCAR-1 CP were pretreated with three indicated drugs (Farlutin, 10 μM) for 24 h before treatment with cisplatin for another 6 h (Scale bar: 5 μm). The localization of NPM1 was detected by immunofluorescence to indicate the ribosomal stress.
Medroxyprogesterone acetate purchased from MedChemExpress. Usage Cited in: Signal Transduct Target Ther. 2023 May 10;8(1):183. [Abstract]
The cells were pretreated with the three indicated drugs for 24 h (Farlutin, 10 μM). Colony-formation assay was used to determine the drug sensitivity to cisplatin.
Medroxyprogesterone acetate purchased from MedChemExpress. Usage Cited in: Signal Transduct Target Ther. 2023 May 10;8(1):183. [Abstract]
Cell viability assay was performed for cisplatin treated ovarian cancer organoids with/without pretreatment with Farlutin, 10 μM, 120 h.
-
Nat Commun
Coronavirus envelope protein activates TMED10-mediated unconventional secretion of inflammatory factors. [Abstract]2024 Oct 8;15(1):8708. PMID: 39379362 -
J Adv Res
Synergistic regulation of SLC7A11 and glucose-6-phosphate dehydrogenase in redox homeostasis governs decidualization: a mechanistic insight into adenomyosis-related infertility. [Abstract]2026 Feb 19:S2090-1232(26)00162-1. PMID: 41722688 -
Redox Biol
GPX4 deficiency-induced ferroptosis drives endometrial epithelial fibrosis in polycystic ovary syndrome. [Abstract]2025 Jun:83:103615. PMID: 40253746 -
Adv Sci (Weinh)
IGFBP5 Restores Endometrial Receptivity and Rescues Implantation Failure in Polycystic Ovary Syndrome. [Abstract]2026 Mar 12:e20455. PMID: 41816941 -
Oncogene
FOXA2 sensitizes endometrial carcinoma to progestin-mediated conservative therapy by triggering PR transcriptional activation. [Abstract]2025 Sep 13. PMID: 40946101 -
EMBO J
TNFSF14+ natural killer cells prevent spontaneous abortion by restricting leucine-mediated decidual stromal cell senescence. [Abstract]2024 Nov;43(21):5018-5036. PMID: 39261664
Medroxyprogesterone acetate purchased from MedChemExpress. Usage Cited in: EMBO J. 2024 Nov;43(21):5018-5036. [Abstract]
Human ESC cell line (hESCs) was treated with 8-bromo-cAMP (0.5 mM) plus Medroxyprogesterone acetate (MPA, 1 μM) for different times, and westernblotting assay was used to detect the expression of CDKN2A, CDKN1A, TP53 (indicator of cell senescence) and PRL.
-
Mol Med
SIRT1-mediated deacetylation of FOXO3 enhances mitophagy and drives hormone resistance in endometrial cancer. [Abstract]2024 Sep 12;30(1):147. PMID: 39266959
Medroxyprogesterone acetate purchased from MedChemExpress. Usage Cited in: Mol Med. 2024 Sep 12;30(1):147. [Abstract]
The growth of subcutaneously transplanted tumors in mice (n=6). Daily intraperitoneal injections (100 mg/kg MA, Medroxyprogesterone acetate) were administered, and tumor size was measured every 4 days to calculate tumor volume.
Medroxyprogesterone acetate purchased from MedChemExpress. Usage Cited in: Mol Med. 2024 Sep 12;30(1):147. [Abstract]
TUNEL staining to detect apoptosis of tumor cells in mice in each group (n=6), daily intraperitoneal injections (100 mg/kg MA, Medroxyprogesterone acetate) were administered.
-
Hum Reprod
Excessive proliferating cell nuclear antigen attenuates endometrial adhesive capacity and decidualization in patients with recurrent implantation failure. [Abstract]2024 May 23:deae111. PMID: 38783610 -
Biochem Pharmacol
miR-29a-3p participates in the pathogenesis of spontaneous abortion by inhibiting trophoblast function targeting COL4A2/COL5A1. [Abstract]2025 Jun 23:117060. PMID: 40562119 -
Reprod Biol Endocrinol
TOP2A deficit-induced abnormal decidualization leads to recurrent implantation failure via the NF-κB signaling pathway. [Abstract]2022 Sep 22;20(1):142. PMID: 36138481 -
Int J Mol Sci
The Enzyme 15-Hydroxyprostaglandin Dehydrogenase Inhibits a Shift to the Mesenchymal Pattern of Trophoblasts and Decidual Stromal Cells Accompanied by Prostaglandin Transporter in Preeclampsia. [Abstract]2023 Mar 7;24(6):5111. PMID: 36982197 -
Toxicology
Cadmium induces spontaneous abortion by impairing endometrial stromal cell decidualization. [Abstract]2025 Jan 29:154069. PMID: 39892737 -
Biochim Biophys Acta Mol Basis Dis
Aberrant TCF21 upregulation in adenomyosis impairs endometrial decidualization by increasing PDE4C expression. [Abstract]2025 Jan;1871(1):167526. PMID: 39326465 -
Virol Sin
Systematic evaluation of HSV-1 Δ34.5Δ47 as a dual-function platform for attenuated HSV-1 vaccine and heterologous antigen delivery. [Abstract]2026 Jan 23:S1995-820X(26)00008-8. PMID: 41581759 -
Cell Signal
Acyl-CoA long-chain synthetase 1 (ACSL1) protects the endometrium from excess palmitic acid stress during decidualization. [Abstract]2024 Dec:124:111438. PMID: 39343116 -
Genes Immun
MTA1-mediated transcriptional repression of Cox2 confers resistance against neutrophil infiltration in endometritis. [Abstract]2026 Mar 10. PMID: 41807815 -
FEBS J
2025 Jul 25. PMID: 40711993 -
Curr Issues Mol Biol
Association between KRAS and PIK3CA Mutations and Progesterone Resistance in Endometriotic Epithelial Cell Line. [Abstract]2024 Apr 19;46(4):3579-3594. PMID: 38666954 -
Reprod Biomed Online
Hsa_circ_0001550 impairs decidualization by regulating the proliferation and apoptosis of endometrial stromal cells. [Abstract]2023 Feb;46(2):225-233. PMID: 36396534 -
Vet Res
Development and characterization of functional sheep endometrial luminal epithelial organoids. [Abstract]2026 Jun 9;57(1):102. PMID: 42265778 -
Endocrinology
BMP4 in Human Endometrial Stromal Cells Can Affect Decidualization by Regulating FOXO1 Expression. [Abstract]2024 Apr 29;165(6):bqae049. PMID: 38679470 -
Arch Biochem Biophys
TET3 inhibits the decidualization of human endometrial stromal cells by regulating ITGA10 transcription through recruiting HDAC1/2. [Abstract]2025 Oct:772:110552. PMID: 40675525 -
J Reprod Immunol
RANKL up-regulated by progesterone aggravates lipopolysaccharide-induced acute lung injury during pregnancy. [Abstract]2023 Feb:155:103788. PMID: 36580846 -
J Reprod Immunol
2022 Jun;151:103623. PMID: 35430461 -
Mol Cell Endocrinol
Embryo-derived human chorionic gonadotropin promotes human decidualization through activating epithelial prostaglandin F2α secretion. [Abstract]2025 May 19:112581. PMID: 40398806 -
Mol Cell Endocrinol
NLRP3 inflammasome-mediated Pyroptosis induce Notch signal activation in endometriosis angiogenesis. [Abstract]2023 Aug 20:574:111952. PMID: 37268099 -
J Proteomics
iTRAQ-based quantitative proteomics reveals dysregulation of fibronectin 1 contributes to impaired endometrial decidualization in recurrent implantation failure. [Abstract]2025 Apr 3:316:105437. PMID: 40187609 -
J Assist Reprod Genet
2024 Jun;41(6):1669-1685. PMID: 38526774 -
Mol Reprod Dev
Decreased OGT Attenuates Endometrial Decidualization and Embryo Implantation by Affecting HIF-1α Stability. [Abstract]2025 May;92(5):e70025. PMID: 40342239 -
-
-
-
-
Solvent & Solubility
DMSO : 10 mg/mL (25.87 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Ethanol : 6.25 mg/mL (16.17 mM; ultrasonic and warming and heat to 60°C)
H2O : < 0.1 mg/mL (insoluble)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 1 mg/mL (2.59 mM); Clear solution
This protocol yields a clear solution of ≥ 1 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (10.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 1 mg/mL (2.59 mM); Clear solution
This protocol yields a clear solution of ≥ 1 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (10.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
For the following dissolution methods, please prepare the working solution directly:
It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 15% Cremophor EL 85% Saline
Solubility: 25 mg/mL (64.68 mM); Suspended solution; Need ultrasonic
Please enter the basic information of animal experiments:
-
-
-
-
Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
-
%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
-
%+
-
+%Tween-80 + +
-
%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Purity & Documentation
-
Data Sheet (280 KB)
-
SDS (419 KB)
- English - EN (419 KB)
- Français - FR (419 KB)
- Deutsch - DE (419 KB)
- Norwegian - NO (419 KB)
- Español - ES (419 KB)
- Swedish - SV (419 KB)
- Italian - IT (419 KB)
- Korean - KR (419 KB)
- Portuguese - PT (419 KB)
-
Handling Instructions (2659 KB)
References
[1]. Schindler AE, et al. Classification and pharmacology of progestins. Maturitas. 2008 Sep-Oct;61(1-2):171-80. [Content Brief]
[2]. Simoncini T, et al. Differential signal transduction of progesterone and medroxyprogesterone acetate in human endothelial cells. Endocrinology. 2004 Dec;145(12):5745-56. [Content Brief]
[3]. Smith D, et al. Pharmacokinetics and bioavailability of medroxyprogesterone acetate in the dog and the rat. Biopharm Drug Dispos. 1993 May;14(4):341-55. [Content Brief]
[4]. Bernardi F, et al. Progesterone and medroxyprogesterone acetate effects on central and peripheral allopregnanolone and beta-endorphin levels. Neuroendocrinology. 2006;83(5-6):348-59. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| Ethanol / DMSO | 1 mM | 2.5872 mL | 12.9359 mL | 25.8719 mL | 64.6797 mL |
| 5 mM | 0.5174 mL | 2.5872 mL | 5.1744 mL | 12.9359 mL | |
| 10 mM | 0.2587 mL | 1.2936 mL | 2.5872 mL | 6.4680 mL | |
| 15 mM | 0.1725 mL | 0.8624 mL | 1.7248 mL | 4.3120 mL | |
| DMSO | 20 mM | 0.1294 mL | 0.6468 mL | 1.2936 mL | 3.2340 mL |
| 25 mM | 0.1035 mL | 0.5174 mL | 1.0349 mL | 2.5872 mL |