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There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 60940-34-3 Chemical Structure| 60940-34-3
Chemical Structure| 60940-34-3
Product Citations

Alternative Products

Product Details of Ebselen

CAS No. :60940-34-3
Formula : C13H9NOSe
M.W : 274.18
SMILES Code : O=C1N(C2=CC=CC=C2)[Se]C3=CC=CC=C13
Synonyms :
SPI-1005; PZ-51; DR 3305
InChI Key :DYEFUKCXAQOFHX-UHFFFAOYSA-N
Pubchem ID :3194

Safety of Ebselen

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301+H331-H373-H410
Precautionary Statements:P260-P264-P270-P271-P273-P301+P310+P330-P304+P340+P311-P314-P391-P403+P233-P405-P501
Class:6.1
UN#:3283
Packing Group:

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description Reference
Bone marrow macrophages (BMMs) 10 µM 1 day Ebselen suppressed RANKL-induced osteoclast differentiation by reducing the phosphorylation of IκB, PI3K, and Akt, thereby decreasing the expression of c-Fos and NFATc1. PMC4807414
RAW264.7 cells 8 μg/mL 1 hour Ebselen significantly suppressed the expressions of inflammatory mediators (IL-1β, IL-6, TNF-α, COX-2, iNOS, and CCL2) and reduced the production of oxidative stress-associated indicators (ROS, NO, and MDA) in fungi-stimulated RAW264.7 cells. PMC11152752
Bone marrow macrophages (BMMs) 10 µM 2 days Ebselen induced apoptosis of osteoclasts in the late stage of osteoclast differentiation by activating caspase-3 and caspase-9. PMC4807414
L6 myotubes 10 µM 20-24 hours Ebselen reduces the catalytic activity of SHIP2 and enhances insulin-induced phosphorylation of Akt PMC8935241
Hepatoma cells (Fao cells) 10 µM 20-24 hours Ebselen reduces the catalytic activity of SHIP2 PMC8935241
HCECs 4–18 μg/mL 24 hours Ebselen promoted cell proliferation at low concentrations (?8 μg/mL) and gradually showed cytotoxic effects at high concentrations (?10 μg/mL). PMC11152752
Human Gingival Fibroblasts (HGFs) 10 μM 24 hours To evaluate the cytotoxicity of Ebselen combined with AgNPs on HGFs, results showed that Ebselen combined with AgNPs up to 20 μg/mL showed no obvious cytotoxicity PMC10759458
Human Gingival Fibroblasts (HGFs) 10 μM 4 hours To evaluate the intracellular bactericidal efficiency of Ebselen combined with silver nanoparticles (AgNPs), results showed that Ebselen significantly enhanced the intracellular bactericidal efficiency of AgNPs PMC10759458

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description Reference
C57BL/Ks-db/db mice db/db diabetic mice Oral 10 mg/kg/day Once daily for 10 weeks Ebselen reduces the activity of SHIP2, improves insulin sensitivity, and decreases lipid peroxidation and inflammation in the liver PMC8935241
C57BL/6 mice Fungal keratitis model Topical administration 8 μg/mL 4 times per day for 3 days Ebselen improved the prognosis of mouse fungal keratitis, reduced the fungal burden in mouse corneas, and significantly decreased the expressions of inflammatory mediators as well as the infiltration of macrophages and neutrophils in the cornea. PMC11152752
ICR mice LPS-induced inflammatory bone loss model Oral 10 mg/kg Every 8 days for 8 days Ebselen restored LPS-induced bone loss and reduced TRAP-positive osteoclast formation in bone tissues. PMC4807414
C57BL/6 mice 5-HT2A receptor function model Intraperitoneal injection 1, 5, 10 mg/kg Acute administration or repeated administration (7 days, twice daily) Ebselen inhibited the behavioural responses (head-twitches and ear scratches) and molecular responses (immediate early gene expression) induced by the 5-HT2A receptor agonist DOI, and enhanced the increase in extracellular 5-HT induced by the SSRI citalopram. PMC6003638
BALB/c mice Cigarette smoke exposure model Oral 10 mg/kg Once daily for 8 weeks Ebselen significantly reduced cigarette smoke-induced lung inflammation and vascular oxidative stress, and restored vascular endothelial function. PMC8074626
BALB/c mice Cigarette smoke-induced COPD model Oral gavage 10 mg/kg Daily for 2 or 6 months Ebselen treatment improved the CS-induced reduction in colonic diameter PMC7676466
BALB/c mice Chronic cigarette smoke exposure and influenza A virus infection model Oral gavage 10 mg/kg Once daily for 3 or 10 days Ebselen abolished the vascular dysfunction caused by influenza A virus in chronic cigarette smoke-exposed mice, and alleviated lung inflammation and T cell infiltration. PMC9069468
BALB/c mice Cigarette smoke exposure and influenza A virus infection model Oral gavage 10 mg/kg Daily for 8 weeks Ebselen significantly alleviated the endothelial dysfunction and inflammation induced by cigarette smoke and influenza A virus infection, and reduced T cell infiltration in the aortic wall. PMC9069468
Wistar rats Experimental periodontitis model Local injection 500 μM Every other day for 2 weeks To evaluate the therapeutic effects of Ebselen combined with AgNPs on experimental periodontitis, results showed that Ebselen combined with AgNPs significantly reduced gingival inflammation and alveolar bone resorption PMC10759458

Clinical Trial:

NCT Number Conditions Phases Recruitment Completion Date Locations
NCT02779192 Noise Induced Hearing Loss Phase 2 Not yet recruiting October 2021 United States, Florida ... More >> University of Miami Not yet recruiting Miami, Florida, United States, 33136 Contact: Michael Hoffer, MD          United States, Kansas University of Kansas Medical Center Not yet recruiting Kansas City, Kansas, United States, 66103 Contact: Hinrich Staecker, MD/PhD          United States, South Carolina MUSC Charleston, South Carolina, United States, 29425 United States, Texas University of Texas Southwestern Not yet recruiting Dallas, Texas, United States, 75390 Contact: Joe Kutz, MD          United States, Washington Sound Pharmaceuticals, Inc. Seattle, Washington, United States, 98103 Less <<
NCT01451853 Lung Cancer H... More >>ead and Neck Cancer Hearing Loss Ototoxicity Tinnitus Neuropathy Less << Phase 2 Not yet recruiting September 23, 2019 United States, Washington ... More >> VA Puget Sound Health Care Not yet recruiting Seattle, Washington, United States, 98108 Contact: Tony S. Quang, M.D.    206-768-5356       Principal Investigator: Tony S Quang, M.D. Less <<
NCT03325790 Meniere's Disease Phase 2 Recruiting December 2018 United States, District of Col... More >>umbia Georgetown University Recruiting Washington, District of Columbia, United States, 20057 Contact: Study Director          United States, Kentucky Advanced ENT & Allergy Recruiting Louisville, Kentucky, United States, 40207 Contact: Study Director          United States, New York ENT and Allergy Associates, LLP Recruiting New York, New York, United States, 10017 Contact: Study Director          United States, South Carolina MUSC Recruiting Charleston, South Carolina, United States, 29425 Contact: Study Director          United States, Texas UT Southwestern Recruiting Dallas, Texas, United States, 75390 Contact: Study Director          United States, Washington Northwest Ear, Inc. Recruiting Seattle, Washington, United States, 98104 Contact: Study Director Less <<
NCT01444846 Temporary Auditory Threshold S... More >>hift Less << Phase 2 Completed - United States, Florida ... More >> University of Florida Gainsville, Florida, United States, 32610 Less <<
NCT02819856 Ototoxicity Phase 1 Phase 2 Enrolling by invitation September 2019 United States, South Carolina ... More >> Medical University of South Carolina Charleston, South Carolina, United States, 29425 Less <<
NCT00762671 Type 1 Diabetes Mellitus ... More >> Type 2 Diabetes Mellitus Less << Phase 2 Phase 3 Completed - United States, Massachusetts ... More >> Brigham and Women's Hosptial Boston, Massachusetts, United States, 02115 Less <<
NCT01452607 Hearing Loss ... More >>Cancer Less << Phase 1 Completed - United States, Nebraska ... More >> MDS Pharma Services Lincoln, Nebraska, United States, 68502 Less <<
NCT03013400 Bipolar Disorder ... More >> Bipolar Disorder, Manic Less << Phase 2 Recruiting June 2020 United Kingdom ... More >> Neurosciences Building, Dept. Psychiatry, Warneford Hospital Recruiting Oxford, Oxfordshire, United Kingdom, OX37JX Contact: Ann L Sharpley, PhD    01865 618321    ann.sharpley@psych.ox.ac.uk    Contact: Clare Williams, RMN    01865 618315    clare.williams@psych.ox.ac.uk    Principal Investigator: Philip J Cowen, FRCPsych Less <<
NCT02603081 Meniere's Disease PHASE1|PHASE2 COMPLETED 2025-08-17 House Clinic, Los Angeles, Cal... More >>ifornia, 90057, United States|New York Otology, New York, New York, 10028, United States|MUSC, Charleston, South Carolina, 29425, United States|Sound Pharmaceuticals, Inc., Seattle, Washington, 98103, United States|Northwest Ear, Seattle, Washington, 98104, United States Less <<

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.65mL

0.73mL

0.36mL

18.24mL

3.65mL

1.82mL

36.47mL

7.29mL

3.65mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

[1]Thenin-Houssier S, de Vera IM, et al. Ebselen, a Small-Molecule Capsid Inhibitor of HIV-1 Replication. Antimicrob Agents Chemother. 2016 Mar 25;60(4):2195-208.

[2]Pavon N, Correa F, et al. Ebselen induces mitochondrial permeability transition because of its interaction with adenine nucleotide translocase. Life Sci. 2015 Oct 15;139:108-13.

[3]Thenin-Houssier S, de Vera IM, Pedro-Rosa L, Brady A, Richard A, Konnick B, Opp S, Buffone C, Fuhrmann J, Kota S, Billack B, Pietka-Ottlik M, Tellinghuisen T, Choe H, Spicer T, Scampavia L, Diaz-Griffero F, Kojetin DJ, Valente ST. Ebselen, a Small-Molecule Capsid Inhibitor of HIV-1 Replication. Antimicrob Agents Chemother. 2016 Mar 25;60(4):2195-208. doi: 10.1128/AAC.02574-15. PMID: 26810656; PMCID: PMC4808204.

[4]Leroux F, Bosc D, Beghyn T, Hermant P, Warenghem S, Landry V, Pottiez V, Guillaume V, Charton J, Herledan A, Urata S, Liang W, Sheng L, Tang WJ, Deprez B, Deprez-Poulain R. Identification of ebselen as a potent inhibitor of insulin degrading enzyme by a drug repurposing screening. Eur J Med Chem. 2019 Oct 1;179:557-566. doi: 10.1016/j.ejmech.2019.06.057. Epub 2019 Jun 24. PMID: 31276900; PMCID: PMC6718346.

[5]Jia ZQ, Li SQ, Qiao WQ, Xu WZ, Xing JW, Liu JT, Song H, Gao ZY, Xing BW, He XJ. Ebselen protects mitochondrial function and oxidative stress while inhibiting the mitochondrial apoptosis pathway after acute spinal cord injury. Neurosci Lett. 2018 Jun 21;678:110-117. doi: 10.1016/j.neulet.2018.05.007. Epub 2018 May 4. PMID: 29733976.

 

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