Trovirdine
Based on 1 publication(s) in Google Scholar
Trovirdine inhibits HIV-1 RT with an IC50 of 7 nM when employing heteropolymeric primer/template (oligo-DNA/ribosomal RNA)and dGTP as substrate.
For research use only. We do not sell to patients.
- Purity: 98.62%
- CAS No.: 149488-17-5
- Formula: C13H13BrN4S
- Molecular Weight:337.24
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
Publications Citing Use of MedChemExpress (MCE) Trovirdine
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Biological Activity
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| C8166 | EC50 |
0.015 μM
Compound: trovirdine
|
Antiviral activity against HIV1 in human C8166 cells assessed as reduction of p24 antigen level
Antiviral activity against HIV1 in human C8166 cells assessed as reduction of p24 antigen level
|
[PMID: 18226532] |
| H9 | IC50 |
0.02 μM
Compound: Trovirdine
|
Inhibitory activity against multidrug resistant HIV-1 strain RT-MDR
Inhibitory activity against multidrug resistant HIV-1 strain RT-MDR
|
[PMID: 10999473] |
| MT4 | CC50 |
60 μM
Compound: Trovirdine
|
Concentration required to reduce the viability of mock-infected MT-4 cells by 50% was determined by MTT method
Concentration required to reduce the viability of mock-infected MT-4 cells by 50% was determined by MTT method
|
[PMID: 12593657] |
| MT4 | EC50 |
0.02 μM
Compound: Trovirdine
|
Concentration required to achieve 50% protection of MT-4 cell from the HIV-1 induced cytopathogenicity was determined by the MTT method
Concentration required to achieve 50% protection of MT-4 cell from the HIV-1 induced cytopathogenicity was determined by the MTT method
|
[PMID: 12593657] |
| MT4 | CC50 |
60 μM
Compound: trovirdine
|
Cytotoxicity against human MT4 cells by MTT assay
Cytotoxicity against human MT4 cells by MTT assay
|
[PMID: 18226532] |
| MT4 | EC50 |
0.02 μM
Compound: trovirdine
|
Antiretroviral activity against HIV1 in human MT4 cells assessed as reduction in virus-induced cytopathogenicity by MTT assay
Antiretroviral activity against HIV1 in human MT4 cells assessed as reduction in virus-induced cytopathogenicity by MTT assay
|
[PMID: 18226532] |
| MT4 | CC50 |
60 μM
Compound: trovirdine
|
Cytotoxicity against mock-infected human MT4 cells by MTT assay
Cytotoxicity against mock-infected human MT4 cells by MTT assay
|
[PMID: 18226533] |
| MT4 | EC50 |
0.02 μM
Compound: trovirdine
|
Antiviral activity against HIV1 in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity by MTT assay
Antiviral activity against HIV1 in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity by MTT assay
|
[PMID: 18226533] |
| MT4 | CC50 |
60 μM
Compound: trovirdine
|
Cytotoxicity against human MT4 cells by MTT method
Cytotoxicity against human MT4 cells by MTT method
|
[PMID: 18502646] |
| MT4 | EC50 |
0.02 μM
Compound: trovirdine
|
Antiviral activity against HIV1 in MT4 cells assessed as reduction of virus induced cytopathogenicity by MTT method
Antiviral activity against HIV1 in MT4 cells assessed as reduction of virus induced cytopathogenicity by MTT method
|
[PMID: 18502646] |
| MT4 | CC50 |
60 μM
Compound: Trovirdine
|
Cytotoxicity against mock-infected human MT4 cells by MTT assay
Cytotoxicity against mock-infected human MT4 cells by MTT assay
|
[PMID: 18954921] |
| MT4 | EC50 |
0.02 μM
Compound: Trovirdine
|
Antiviral activity against wild type HIV1 3B in human MT4 cells assessed as protection against viral induced cytopathogenicity by MTT assay
Antiviral activity against wild type HIV1 3B in human MT4 cells assessed as protection against viral induced cytopathogenicity by MTT assay
|
[PMID: 18954921] |
| MT4 | EC50 |
15 μM
Compound: Trovirdine
|
Antiviral activity against HIV1 3B Y181C resistant mutant in human MT4 cells assessed as protection against viral induced cytopathogenicity by MTT assay
Antiviral activity against HIV1 3B Y181C resistant mutant in human MT4 cells assessed as protection against viral induced cytopathogenicity by MTT assay
|
[PMID: 18954921] |
| MT4 | CC50 |
60 μM
Compound: Trovirdine
|
Cytotoxicity against human MT4 cells by MTT assay
Cytotoxicity against human MT4 cells by MTT assay
|
[PMID: 19058881] |
| MT4 | EC50 |
0.02 μM
Compound: Trovirdine
|
Antiviral activity against HIV1 3B infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity by MTT assay
Antiviral activity against HIV1 3B infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity by MTT assay
|
[PMID: 19058881] |
| MT4 | EC50 |
0.12 μM
Compound: Trovirdine
|
Antiviral activity against HIV1 3B expressing reverse transcriptase Y181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity by MTT assay
Antiviral activity against HIV1 3B expressing reverse transcriptase Y181C mutant infected in human MT4 cells assessed as inhibition of virus-induced cytopathogenicity by MTT assay
|
[PMID: 19058881] |
| MT4 | ED50 |
0.02 μM
Compound: LY-300046
|
Tested for the inhibition of wild type HIV-1 (IIIB) replication in MT-4 cells
Tested for the inhibition of wild type HIV-1 (IIIB) replication in MT-4 cells
|
[PMID: 8863804] |
| MT4 | ED50 |
>5 μM
Compound: Trovirdine
|
Antiviral activity was determined against HIV-1 (clone 90) in MT-4 cells infected with HIV-1 IIIB using an XTT assay
Antiviral activity was determined against HIV-1 (clone 90) in MT-4 cells infected with HIV-1 IIIB using an XTT assay
|
[PMID: 9873380] |
| MT4 | ED50 |
0.8 μM
Compound: Trovirdine
|
Antiviral activity was determined against HIV-1 (clone 118) in MT-4 cells infected with HIV-1 IIIB using an XTT assay
Antiviral activity was determined against HIV-1 (clone 118) in MT-4 cells infected with HIV-1 IIIB using an XTT assay
|
[PMID: 9873380] |
| MT4 | CC50 |
60 μM
Compound: Trovirdine
|
Cytotoxicity against mock infected Homo sapiens (human) MT4 cells assessed as cell viability by MTT assay
Cytotoxicity against mock infected Homo sapiens (human) MT4 cells assessed as cell viability by MTT assay
|
10.1007/s00044-009-9192-x |
| MT4 | EC50 |
0.02 μM
Compound: Trovirdine
|
Antiviral activity against wild type Human immunodeficiency virus 1 infected human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 4 days by MTT assay
Antiviral activity against wild type Human immunodeficiency virus 1 infected human MT4 cells assessed as inhibition of virus-induced cytopathic effect after 4 days by MTT assay
|
10.1007/s00044-009-9192-x |
Chemical Information
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CAS No. 149488-17-5
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Appearance Solid
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Molecular Weight 337.24
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Formula C13H13BrN4S
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Color White to off-white
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SMILES
S=C(NCCC1=NC=CC=C1)NC2=NC=C(Br)C=C2
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Synonyms
LY300046
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year
Publications (1)
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Journal Impact Factor
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Most Recent
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Int J Antimicrob Agents
2019 Dec;54(6):814-819. PMID: 31479744
Solvent & Solubility
DMSO : 100 mg/mL (296.52 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
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: ≥ 2.5 mg/mL (7.41 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 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.
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:
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%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.
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
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Data Sheet (268 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 2.9652 mL | 14.8262 mL | 29.6525 mL | 74.1312 mL |
| 5 mM | 0.5930 mL | 2.9652 mL | 5.9305 mL | 14.8262 mL | |
| 10 mM | 0.2965 mL | 1.4826 mL | 2.9652 mL | 7.4131 mL | |
| 15 mM | 0.1977 mL | 0.9884 mL | 1.9768 mL | 4.9421 mL | |
| 20 mM | 0.1483 mL | 0.7413 mL | 1.4826 mL | 3.7066 mL | |
| 25 mM | 0.1186 mL | 0.5930 mL | 1.1861 mL | 2.9652 mL | |
| 30 mM | 0.0988 mL | 0.4942 mL | 0.9884 mL | 2.4710 mL | |
| 40 mM | 0.0741 mL | 0.3707 mL | 0.7413 mL | 1.8533 mL | |
| 50 mM | 0.0593 mL | 0.2965 mL | 0.5930 mL | 1.4826 mL | |
| 60 mM | 0.0494 mL | 0.2471 mL | 0.4942 mL | 1.2355 mL | |
| 80 mM | 0.0371 mL | 0.1853 mL | 0.3707 mL | 0.9266 mL | |
| 100 mM | 0.0297 mL | 0.1483 mL | 0.2965 mL | 0.7413 mL |