Hydrocortisone
Based on 85 publication(s) in Google Scholar
Hydrocortisone (Cortisol) is a steroid hormone or glucocorticoid secreted by the adrenal cortex.
For research use only. We do not sell to patients.
- Purity: 99.92%
- CAS No.: 50-23-7
- Formula: C21H30O5
- Molecular Weight:362.46
-
Storage:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Publications Citing Use of MedChemExpress (MCE) Hydrocortisone
More- Signal Transduct Target Ther. 2025 Nov 4;10(1):361. [Abstract]
- Signal Transduct Target Ther. 2025 Jul 9;10(1):217. [Abstract]
- Nature. 2021 Jan;589(7843):620-626. [Abstract]
- Cell. 2025 Jan 9;188(1):157-174.e22. [Abstract]
- Cell Metab. 2024 Nov 5;36(11):2402-2418.e10. [Abstract]
- Cancer Commun (Lond). 2021 Jul;41(7):576-595. [Abstract]
- Cell Stem Cell. 2025 Mar 20:S1934-5909(25)00084-0. [Abstract]
- Nat Commun. 2025 Aug 7;16(1):7287. [Abstract]
- Nat Commun. 2024 Oct 8;15(1):8708. [Abstract]
- Adv Sci (Weinh). 2024 Dec 24:e2413514. [Abstract]
- Nat Chem Biol. 2022 Nov;18(11):1196-1203. [Abstract]
- Sci Adv. 2025 Jun 20;11(25):eadt3075. [Abstract]
- Sci Adv. 2025 May 9;11(19):eadr3173. [Abstract]
- Sci Adv. 2023 Oct 6;9(40):eadi6586. [Abstract]
- Cell Death Dis. 2025 Dec 22;16(1):918. [Abstract]
- Acta Biomater. 2025 Nov 25:S1742-7061(25)00880-3. [Abstract]
- Adv Healthc Mater. 2025 Apr;14(9):e2404388. [Abstract]
- Sci China Life Sci. 2026 Mar 20. [Abstract]
- Proc Natl Acad Sci U S A. 2026 Mar 10;123(10):e2518983123. [Abstract]
- Cell Commun Signal. 2025 Mar 7;23(1):124. [Abstract]
- J Pharm Anal. 2024 Jul;14(7):100934. [Abstract]
- Int J Biol Macromol. 2026 Mar:349:150861. [Abstract]
- Int J Biol Macromol. 2025 Dec;334(Pt 2):149132. [Abstract]
- Int J Biol Macromol. 2024 Feb 5;262(Pt 1):129875. [Abstract]
- EMBO Mol Med. 2025 Jul;17(7):1794-1824. [Abstract]
- Free Radic Biol Med. 2026 Mar 16:246:316-333. [Abstract]
- Br J Pharmacol. 2023 Aug;180(15):1930-1948. [Abstract]
- Sci Signal. 2025 Oct 21;18(909):eadx2532. [Abstract]
- Ecotoxicol Environ Saf. 2025 Sep 15:303:118984. [Abstract]
- Ecotoxicol Environ Saf. 2024 Jul 2:281:116680. [Abstract]
- JCI Insight. 2021 Jun 22;6(12):e142838. [Abstract]
- J Mol Cell Biol. 2025 Jul 22:mjaf019. [Abstract]
- Cell Biol Toxicol. 2025 May 15;41(1):85. [Abstract]
- Biochem Pharmacol. 2025 Jul 12:241:117165. [Abstract]
- Biochem Pharmacol. 2025 Apr:234:116822. [Abstract]
- J Ethnopharmacol. 2024 Nov 1:119025. [Abstract]
- Lab Chip. 2025 Mar 25;25(7):1656-1668. [Abstract]
- J Ethnopharmacol. 2022 May 10;289:115018. [Abstract]
- Chem Biol Interact. 2022 Feb 25:354:109798. [Abstract]
- J Pathol. 2025 Jul;266(3):306-321. [Abstract]
- Immunology. 2025 Sep 6. [Abstract]
- Biomed Signal Process Control. 2026 Feb 26.
- Int J Mol Sci. 2025 Jul 25;26(15):7183. [Abstract]
- Int J Mol Sci. 2023 May 16;24(10):8841. [Abstract]
- Invest Ophthalmol Vis Sci. 2026 Jan 5;67(1):6. [Abstract]
- J Mol Cell Cardiol. 2025 Feb:199:104-117. [Abstract]
- Eur J Pharmacol. 2023 Feb 15:941:175499. [Abstract]
- Biol Res. 2024 Nov 24;57(1):90. [Abstract]
- Front Endocrinol. 2022 Feb 24;13:816229. [Abstract]
- Cancers (Basel). 2022 Aug 18;14(16):3986. [Abstract]
- iScience. 2023 Aug 29;26(10):107773. [Abstract]
- iScience. 2023 Apr 5,23.
- iScience. 2023 Apr 18;26(5):106688. [Abstract]
- Chem Res Toxicol. 2025 Aug 11. [Abstract]
- Food Sci Nutr. 2022 Jan 18;10(2):564-576. [Abstract]
- Mol Cell Biochem. 2024 Dec;479(12):3447-3458. [Abstract]
- Mol Cell Endocrinol. 2022 May 1:547:111597. [Abstract]
- Exp Cell Res. 2020 Aug 1;393(1):112054. [Abstract]
- Toxicol Appl Pharmacol. 2026 Jan:506:117659. [Abstract]
- Toxicol Appl Pharmacol. 2025 Sep 5:505:117545. [Abstract]
- Endocrinology. 2026 May 6;167(6):bqag055. [Abstract]
- Cell Stress Chaperones. 2025 Sep 17:100112. [Abstract]
- Mol Carcinog. 2025 Mar 26. [Abstract]
- Immunopharmacol Immunotoxicol. 2022 Oct;44(5):786-794. [Abstract]
- J Anim Sci. 2025 Jan 4:103:skaf374. [Abstract]
- Int J Biochem Cell Biol. 2023 Apr:157:106389. [Abstract]
- Immun Inflamm Dis. 2025 Aug;13(8):e70229. [Abstract]
- Adv Biol (Weinh). 2023 Sep;7(9):e2200130. [Abstract]
- Cancer Manag Res. 2019 Jun 21:11:5557-5572. [Abstract]
- Tissue Cell. 2022 Dec:79:101915. [Abstract]
- Exp Ther Med. 2021 Aug;22(2):829. [Abstract]
- Biochem Biophys Res Commun. 2024 Jul 18:733:150421. [Abstract]
- Oncol Lett. 2021 Jul;22(1):498. [Abstract]
- Otol Neurotol. 2024 Jan 1;45(1):e49-e56. [Abstract]
- Oral Surg Oral Med Oral Pathol Oral Radiol. 2025 Sep 17:S2212-4403(25)01212-X. [Abstract]
- Mutat Res. 2025 Jun 11:831:111911. [Abstract]
- Patent. US20250368964A1.
- bioRxiv. 2025 Nov 5.
- bioRxiv. 2025 Oct 14.
- bioRxiv. 2024 Feb 10.
- Research Square Preprint. 2023 Apr 10.
- Research Square Print. December 5th, 2022.
- Research Square Preprint. 2022 Jul.
- Oxid Med Cell Longev. 2022 Jan 27:2022:7502632. [Abstract]
- Universidade de São Paulo. 2020 Sep.
All Endogenous Metabolite Isoforms
More
Biological Activity
|
Human Endogenous Metabolite |
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | IC50 |
>20 μM
Compound: HYD
|
Cytotoxicity against human A549 cells after 72 hrs by MTT assay
Cytotoxicity against human A549 cells after 72 hrs by MTT assay
|
[PMID: 26695732] |
| B16-F10 | IC50 |
>20 μM
Compound: HYD
|
Cytotoxicity against mouse B16F10 cells after 72 hrs by MTT assay
Cytotoxicity against mouse B16F10 cells after 72 hrs by MTT assay
|
[PMID: 26695732] |
| COS-7 | IC50 |
>20 μM
Compound: HYD
|
Cytotoxicity against african green monkey COS1 cells after 72 hrs by MTT assay
Cytotoxicity against african green monkey COS1 cells after 72 hrs by MTT assay
|
[PMID: 26695732] |
| HeLa | IC50 |
>20 μM
Compound: HYD
|
Cytotoxicity against human HeLa cells after 72 hrs by MTT assay
Cytotoxicity against human HeLa cells after 72 hrs by MTT assay
|
[PMID: 26695732] |
| LLC-PK1 | IC50 |
>50 μM
Compound: Hydrocortisone
|
Inhibition of P-glycoprotein, human L-MDR1 expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, human L-MDR1 expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389] |
| LLC-PK1 | IC50 |
>50 μM
Compound: Hydrocortisone
|
Inhibition of P-glycoprotein, mouse L-mdr1a expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, mouse L-mdr1a expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389] |
| LLC-PK1 | IC50 |
>50 μM
Compound: Hydrocortisone
|
Inhibition of P-glycoprotein, mouse L-mdr1b expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
Inhibition of P-glycoprotein, mouse L-mdr1b expressed in LLC-PK1 epithelial cells using calcein-AM polarisation assay
|
[PMID: 12699389] |
| LLC-PK1 | IC50 |
>50 μM
Compound: Hydrocortisone
|
TP_TRANSPORTER: inhibition of Calcein-AM efflux in Mdr1a-expressing LLC-PK1 cells
TP_TRANSPORTER: inhibition of Calcein-AM efflux in Mdr1a-expressing LLC-PK1 cells
|
[PMID: 12699389] |
| LLC-PK1 | IC50 |
>50 μM
Compound: Hydrocortisone
|
TP_TRANSPORTER: inhibition of Calcein-AM efflux in Mdr1b-expressing LLC-PK1 cells
TP_TRANSPORTER: inhibition of Calcein-AM efflux in Mdr1b-expressing LLC-PK1 cells
|
[PMID: 12699389] |
| LLC-PK1 | IC50 |
>50 μM
Compound: Hydrocortisone
|
TP_TRANSPORTER: inhibition of Calcein-AM efflux in MDR1-expressing LLC-PK1 cells
TP_TRANSPORTER: inhibition of Calcein-AM efflux in MDR1-expressing LLC-PK1 cells
|
[PMID: 12699389] |
| Macrophage | IC50 |
10 nM
Compound: Hydrocortisone
|
Antiinflammatory activity in CD-1 mouse Macrophage assessed as inhibition of IFN-gamma induced NO production after 48 hrs by Griess reaction
Antiinflammatory activity in CD-1 mouse Macrophage assessed as inhibition of IFN-gamma induced NO production after 48 hrs by Griess reaction
|
[PMID: 21361338] |
| MCF7 | IC50 |
>20 μM
Compound: HYD
|
Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay
Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay
|
[PMID: 26695732] |
| NIH3T3 | IC50 |
>20 μM
Compound: HYD
|
Cytotoxicity against mouse NIH/3T3 cells after 72 hrs by MTT assay
Cytotoxicity against mouse NIH/3T3 cells after 72 hrs by MTT assay
|
[PMID: 26695732] |
| RAW264.7 | IC50 |
>20 μM
Compound: HYD
|
Cytotoxicity against mouse RAW264.7 cells after 72 hrs by MTT assay
Cytotoxicity against mouse RAW264.7 cells after 72 hrs by MTT assay
|
[PMID: 26695732] |
| RAW264.7 | IC50 |
3.26 μM
Compound: Hydrocortisone
|
Anti-inflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production in macrophages
Anti-inflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production in macrophages
|
[PMID: 32485533] |
| RAW264.7 | IC50 |
3.4 μM
Compound: Hydrocortisone
|
Inhibition of NO production in LPS-stimulated mouse RAW264.7 cells incubated for 24 hrs by Griess reagent-based assay
Inhibition of NO production in LPS-stimulated mouse RAW264.7 cells incubated for 24 hrs by Griess reagent-based assay
|
[PMID: 33454546] |
| RAW264.7 | IC50 |
40.64 μM
Compound: Hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production by MTT assay
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production by MTT assay
|
[PMID: 20879743] |
| RAW264.7 | IC50 |
40.64 μM
Compound: Hydrocortisone
|
Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells after 24 hrs by Griess reaction based spectrophotometry
Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells after 24 hrs by Griess reaction based spectrophotometry
|
[PMID: 21807513] |
| RAW264.7 | IC50 |
40.64 μM
Compound: Hydrocortisone
|
Inhibition of LPS-induced NO production in mouse RAW264.7 cells after 24 hrs by Griess reaction
Inhibition of LPS-induced NO production in mouse RAW264.7 cells after 24 hrs by Griess reaction
|
[PMID: 23067550] |
| RAW264.7 | IC50 |
43.8 μM
Compound: Hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess assay
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess assay
|
[PMID: 23755850] |
| RAW264.7 | IC50 |
5.5 μM
Compound: Hydrocortisone
|
Antiinflammatory activity against mouse RAW264.7 cells assessed as inhibition of LPS-induced PGE2 production preincubated for 1 hr followed by LPS-stimulation and measured after 18 hrs
Antiinflammatory activity against mouse RAW264.7 cells assessed as inhibition of LPS-induced PGE2 production preincubated for 1 hr followed by LPS-stimulation and measured after 18 hrs
|
[PMID: 31126853] |
| RAW264.7 | IC50 |
51.4 μM
Compound: hydrocortisone
|
Inhibition of LPS-induced NO production in mouse RAW264.7 cells by Griess assay
Inhibition of LPS-induced NO production in mouse RAW264.7 cells by Griess assay
|
[PMID: 25275213] |
| RAW264.7 | IC50 |
52.43 μM
Compound: Hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production preincubated for 3 hrs followed by LPS addition measured after 24 hrs by Griess assay
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production preincubated for 3 hrs followed by LPS addition measured after 24 hrs by Griess assay
|
[PMID: 31009914] |
| RAW264.7 | IC50 |
53.7 μM
Compound: hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of NO production after 24 hrs by Griess assay
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of NO production after 24 hrs by Griess assay
|
[PMID: 25076059] |
| RAW264.7 | IC50 |
53.8 μM
Compound: Hydrocortisone
|
Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells treated 1 hr before LPS challenge measured after 24 hrs by Griess reaction method
Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells treated 1 hr before LPS challenge measured after 24 hrs by Griess reaction method
|
[PMID: 23294419] |
| RAW264.7 | IC50 |
54.23 μM
Compound: Hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess method
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess method
|
[PMID: 24660966] |
| RAW264.7 | IC50 |
54.23 μM
Compound: Hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production after 24 hrs by Griess method
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production after 24 hrs by Griess method
|
[PMID: 26615888] |
| RAW264.7 | IC50 |
58.79 μM
Compound: Hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess assay
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess assay
|
[PMID: 27256914] |
| RAW264.7 | IC50 |
58.79 μM
Compound: Hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess assay
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs by Griess assay
|
[PMID: 27295506] |
| RAW264.7 | IC50 |
58.79 μM
Compound: Hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production preincubated for 3 hrs followed by LPS addition and measured after 24 hrs by griess assay
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production preincubated for 3 hrs followed by LPS addition and measured after 24 hrs by griess assay
|
[PMID: 30419492] |
| RAW264.7 | IC50 |
61 nM
Compound: Hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of IFN-gamma induced NO production after 24 hrs by Griess reaction
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of IFN-gamma induced NO production after 24 hrs by Griess reaction
|
[PMID: 21361338] |
| RAW264.7 | IC50 |
63.86 μM
Compound: hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced IL-6 production by ELISA
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced IL-6 production by ELISA
|
[PMID: 20095629] |
| RAW264.7 | IC50 |
64.34 μM
Compound: hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 assessed as inhibition LPS-induced nitric oxide production cells after 24 hrs
Antiinflammatory activity in mouse RAW264.7 assessed as inhibition LPS-induced nitric oxide production cells after 24 hrs
|
[PMID: 20095629] |
| RAW264.7 | IC50 |
64.34 μM
Compound: Hydrocortisone
|
Inhibition of nitric oxide production in lipopolysaccharide-activated mouse RAW264.7 cells by Griess reaction based method
Inhibition of nitric oxide production in lipopolysaccharide-activated mouse RAW264.7 cells by Griess reaction based method
|
[PMID: 23305920] |
| RAW264.7 | IC50 |
64.34 μM
Compound: hydrocortisone
|
Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells assessed as nitrite formation
Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells assessed as nitrite formation
|
[PMID: 18348534] |
| RAW264.7 | IC50 |
85.64 μM
Compound: hydrocortisone
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced TNFalpha production by ELISA
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced TNFalpha production by ELISA
|
[PMID: 20095629] |
| SK-OV-3 | IC50 |
>20 μM
Compound: HYD
|
Cytotoxicity against human SKOV3 cells after 72 hrs by MTT assay
Cytotoxicity against human SKOV3 cells after 72 hrs by MTT assay
|
[PMID: 26695732] |
Hydrocortisone (50 nM) shows a dose-dependent down-regulation of GR transcript in hCMEC/D3 cells. Hydrocortisone supplementation of the serum-reduced cell differentiation medium leads to a significant increase in TER across the hCMEC/D3 monolayer[1]. Hydrocortisone-treated Dendritic cells (DCs) show a decreased expression of MHC II molecules, the costimulatory molecule CD86, and the DC-specific marker CD83, as well as a strongly reduced IL-12 secretion. Hydrocortisone-treated DCs inhibit production of IFN-γ but induce an increased release of IL-4 and no change in IL-5[2]. Hydrocortisone reduces postischemic oxidative stress, perfusion pressure, and transudate formation. Hydrocortisone inhibits postischemic shedding of syndecan-1, heparan sulfate, and hyaluronan as is release of histamine from resident mast cells[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
Chemical Information
-
CAS No. 50-23-7
-
Appearance Solid
-
Molecular Weight 362.46
-
Formula C21H30O5
-
Color White to off-white
-
SMILES
C[C@@]1([C@@]2(O)C(CO)=O)[C@](CC2)([H])[C@@](CCC3=CC4=O)([H])[C@]([C@]3(CC4)C)([H])[C@@H](O)C1
-
Synonyms
Cortisol
-
Structure Classification
-
Initial Source
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Publications (85)
-
Journal Impact Factor
-
Most Recent
-
Signal Transduct Target Ther
Olverembatinib, a multikinase inhibitor that modulates lipid metabolism, in advanced succinate dehydrogenase-deficient gastrointestinal stromal tumors: a phase 1b study and translational research. [Abstract]2025 Nov 4;10(1):361. PMID: 41184234 -
Signal Transduct Target Ther
A novel peptide 66CTG stabilizes Myc proto-oncogene protein to promote triple-negative breast cancer growth. [Abstract]2025 Jul 9;10(1):217. PMID: 40628713 -
Nature
2021 Jan;589(7843):620-626. PMID: 33408414 -
Cell
Intermittent fasting triggers interorgan communication to suppress hair follicle regeneration. [Abstract]2025 Jan 9;188(1):157-174.e22. PMID: 39674178 -
Cell Metab
Sensing steroid hormone 17α-hydroxypregnenolone by GPR56 enables protection from ferroptosis-induced liver injury. [Abstract]2024 Nov 5;36(11):2402-2418.e10. PMID: 39389061 -
Cancer Commun (Lond)
YB1 regulates miR-205/200b-ZEB1 axis by inhibiting microRNA maturation in hepatocellular carcinoma. [Abstract]2021 Jul;41(7):576-595. PMID: 34110104 -
Cell Stem Cell
Vagal pathway activation links chronic stress to decline in intestinal stem cell function. [Abstract]2025 Mar 20:S1934-5909(25)00084-0. PMID: 40120585 -
Nat Commun
Galectin-3-integrin α5β1 phase separation disrupted by advanced glycation end-products impairs diabetic wound healing in rodents. [Abstract]2025 Aug 7;16(1):7287. PMID: 40775187 -
Nat Commun
Coronavirus envelope protein activates TMED10-mediated unconventional secretion of inflammatory factors. [Abstract]2024 Oct 8;15(1):8708. PMID: 39379362 -
Adv Sci (Weinh)
Targeting CDK2 Confers Vulnerability to Lenvatinib Via Driving Senescence in Anaplastic Thyroid Cancer. [Abstract]2024 Dec 24:e2413514. PMID: 39716890 -
Nat Chem Biol
2022 Nov;18(11):1196-1203. PMID: 35982227 -
Sci Adv
FAM50A drives breast cancer brain metastasis through interaction with C9ORF78 to enhance ʟ-asparagine production. [Abstract]2025 Jun 20;11(25):eadt3075. PMID: 40531994 -
Sci Adv
Targeting PSMD14 combined with arachidonic acid induces synthetic lethality via FADS1 m6A modification in triple-negative breast cancer. [Abstract]2025 May 9;11(19):eadr3173. PMID: 40344056 -
Sci Adv
Human cytomegalovirus UL36 inhibits IRF3-dependent immune signaling to counterbalance its immunoenhancement as apoptotic inhibitor. [Abstract]2023 Oct 6;9(40):eadi6586. PMID: 37792941 -
Cell Death Dis
2025 Dec 22;16(1):918. PMID: 41430036 -
Acta Biomater
A physiological oxygen gradient liver-zonation-on-a-chip reveals HIF-2α intervention in hepatic lipotoxicity. [Abstract]2025 Nov 25:S1742-7061(25)00880-3. PMID: 41308852 -
Adv Healthc Mater
2025 Apr;14(9):e2404388. PMID: 40018834 -
Sci China Life Sci
SIRT6 alleviates ischemic injury via orchestrating the RREB1/Snail and STC1/Smad7 signaling pathways to regulate endothelial-mesenchymal transition. [Abstract]2026 Mar 20. PMID: 41882317 -
Proc Natl Acad Sci U S A
Neutralization of acyl-CoA-binding protein attenuates glucocorticoid-mediated suppression of cancer immunosurveillance. [Abstract]2026 Mar 10;123(10):e2518983123. PMID: 41779791 -
Cell Commun Signal
Extracellular vesicular delivery of ceramides from pulmonary macrophages to endothelial cells facilitates chronic obstructive pulmonary disease. [Abstract]2025 Mar 7;23(1):124. PMID: 40055817 -
J Pharm Anal
Baicalin reduces chronic stress-induced breast cancer metastasis via directly targeting β2-adrenergic receptor. [Abstract]2024 Jul;14(7):100934. PMID: 39139999 -
Int J Biol Macromol
E3 ubiquitin ligase DTX3L promotes breast cancer progression by enhancing PKCα ubiquitination and inhibiting the p38 MAPK signaling pathway. [Abstract]2026 Mar:349:150861. PMID: 41679478 -
Int J Biol Macromol
Circular RNA circPTPN3 facilitates duck hepatitis A virus type 3 (DHAV-3) infection by reducing miR-130b-5p function in duck. [Abstract]2025 Dec;334(Pt 2):149132. PMID: 41265597 -
Int J Biol Macromol
Linc-smad7 is involved in the regulation of lipid synthesis in mouse mammary epithelial cells. [Abstract]2024 Feb 5;262(Pt 1):129875. PMID: 38320638 -
EMBO Mol Med
NRF2 modulates WNT signaling pathway to enhance photodynamic therapy resistance in oral leukoplakia. [Abstract]2025 Jul;17(7):1794-1824. PMID: 40494896 -
Free Radic Biol Med
Chronic stress-induced steroids mediate mitochondrial fission and fibrosis in the trabecular meshwork via the MIEF1-MAOA complex. [Abstract]2026 Mar 16:246:316-333. PMID: 41579974 -
Br J Pharmacol
A novel sorbicillinoid compound as a potent anti-inflammation agent through inducing NLRP3 protein degradation. [Abstract]2023 Aug;180(15):1930-1948. PMID: 36788033 -
Sci Signal
PARP1-mediated PARylation of TEAD4 stabilizes the YAP1-TEAD4 complex and promotes growth and immune evasion in breast cancer cells. [Abstract]2025 Oct 21;18(909):eadx2532. PMID: 41118450 -
Ecotoxicol Environ Saf
Blue light pollution induces dry eye by damaging conjunctival stem cells through cAMP-PKA-Pax6 signaling pathway. [Abstract]2025 Sep 15:303:118984. PMID: 40912100 -
Ecotoxicol Environ Saf
Impaired GPX4 activity elicits ferroptosis in alveolar type II cells promoting PHMG-induced pulmonary fibrosis development. [Abstract]2024 Jul 2:281:116680. PMID: 38964057 -
JCI Insight
Pdcd10-Stk24/25 complex controls kidney water reabsorption by regulating Aqp2 membrane targeting. [Abstract]2021 Jun 22;6(12):e142838. PMID: 34156031 -
J Mol Cell Biol
The mechanoresponsive chromosomal passenger complex sustains furrow ingression under confinement. [Abstract]2025 Jul 22:mjaf019. PMID: 40693957 -
Cell Biol Toxicol
IGFBP3 enhances adipose-derived stem cell function in soft tissue injury repair via ITGB1 and ERK pathway activation. [Abstract]2025 May 15;41(1):85. PMID: 40369223 -
Biochem Pharmacol
Adaptively increased intake of arginine sustains oral keratinocyte survival through alleviating oxidative stress during targeting glutamine metabolism. [Abstract]2025 Jul 12:241:117165. PMID: 40659135 -
Biochem Pharmacol
TRIM21 knockout alleviates renal fibrosis by promoting autophagic degradation of mature TGF-β1. [Abstract]2025 Apr:234:116822. PMID: 39983846 -
J Ethnopharmacol
Glycyrrhizic acid and patchouli alcohol in Huoxiang Zhengqi attenuate intestinal inflammation and barrier injury via regulating endogenous corticosterone metabolism mediated by 11β-HSD1. [Abstract]2024 Nov 1:119025. PMID: 39489360 -
Lab Chip
Revealing transport, uptake and damage of polystyrene microplastics using a gut-liver-on-a-chip. [Abstract]2025 Mar 25;25(7):1656-1668. PMID: 39589486 -
J Ethnopharmacol
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Solvent & Solubility
DMSO : 200 mg/mL (551.79 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Ethanol : 5 mg/mL (13.79 mM; Need ultrasonic)
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, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
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, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
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: ≥ 2.08 mg/mL (5.74 mM); Clear solution
This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 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: ≥ 2.08 mg/mL (5.74 mM); Clear solution
This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 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.
Please enter the basic information of animal experiments:
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-
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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.
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%+
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+%Tween-80 + +
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%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. * In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
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.
Protocol
Cells are plated on top of collagen IV-coated transwell chambers for six-well plates (24 mm diameter, membrane material: polyethylene terephthalate (PET), 0.4 μm pores, pore density 1.6×106 cm2) at densities of 2.5×104 cells cm2 per well. When they have reached confluence at day 5, the different experimental sets of cells are transferred to differentiation medium containing reduced amounts of FCS and treated with TNFα or hydrocortisone as indicated.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Purity & Documentation
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Data Sheet (279 KB)
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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)
- Portuguese - PT (419 KB)
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Handling Instructions (2659 KB)
References
[1]. Förster C, et al. Differential effects of hydrocortisone and TNFalpha on tight junction proteins in an in vitro model of the human blood-brain barrier. J Physiol. 2008 Apr 1;586(7):1937-49. [Content Brief]
[2]. Bellinghausen I, et al. Inhibition of human allergic T-cell responses by IL-10-treated dendritic cells: differences from hydrocortisone-treated dendritic cells. J Allergy Clin Immunol. 2001 Aug;108(2):242-9. [Content Brief]
[3]. Chappell D, et al. Hydrocortisone preserves the vascular barrier by protecting the endothelial glycocalyx. Anesthesiology. 2007 Nov;107(5):776-84. [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, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| Ethanol / DMSO | 1 mM | 2.7589 mL | 13.7946 mL | 27.5893 mL | 68.9731 mL |
| 5 mM | 0.5518 mL | 2.7589 mL | 5.5179 mL | 13.7946 mL | |
| 10 mM | 0.2759 mL | 1.3795 mL | 2.7589 mL | 6.8973 mL | |
| DMSO | 15 mM | 0.1839 mL | 0.9196 mL | 1.8393 mL | 4.5982 mL |
| 20 mM | 0.1379 mL | 0.6897 mL | 1.3795 mL | 3.4487 mL | |
| 25 mM | 0.1104 mL | 0.5518 mL | 1.1036 mL | 2.7589 mL | |
| 30 mM | 0.0920 mL | 0.4598 mL | 0.9196 mL | 2.2991 mL | |
| 40 mM | 0.0690 mL | 0.3449 mL | 0.6897 mL | 1.7243 mL | |
| 50 mM | 0.0552 mL | 0.2759 mL | 0.5518 mL | 1.3795 mL | |
| 60 mM | 0.0460 mL | 0.2299 mL | 0.4598 mL | 1.1496 mL | |
| 80 mM | 0.0345 mL | 0.1724 mL | 0.3449 mL | 0.8622 mL | |
| 100 mM | 0.0276 mL | 0.1379 mL | 0.2759 mL | 0.6897 mL |