1. Cell Cycle/DNA Damage Autophagy Apoptosis Anti-infection
  2. DNA/RNA Synthesis Autophagy Apoptosis HIV Orthopoxvirus
  3. Hydroxyurea

ヒドロキシカルバミド  (Synonyms: Hydroxyurea)

製品番号: HY-B0313 純度: 99.34%
COA 取扱説明書 Technical Support

Hydroxyurea is a cell apoptosis inducer that inhibit DNA synthesis through inhibition of ribonucleotide reductase. Hydroxyurea shows anti-orthopoxvirus activity.

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研究用途以外に使用した場合、当社は一切の責任を負いかねます。

CAS 番号 : 127-07-1

容量 価格(税別) 在庫状況 数量
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
USD 60 在庫あり
Solution
10 mM * 1 mL in DMSO USD 60 在庫あり
Solid
500 mg $55 在庫あり
1 g $66 在庫あり
5 g $86 在庫あり
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50 g   お問い合わせ  

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カスタマーレビュー

Based on 31 publication(s) in Google Scholar

Other Forms of Hydroxyurea:

Top Publications Citing Use of Products

顧客検証

WB
IP
Cell Imaging/Staining
RT-PCR
Cell Proliferation/Viability Assay

    Hydroxyurea purchased from MedChemExpress. Usage Cited in: Mol Cancer. 2024 Apr 29;23(1):86.  [Abstract]

    The cell viability of the indicated T24 cells was determined after 48 h of continuous exposure to multiple concentrations of hydroxyurea (HU).

    Hydroxyurea purchased from MedChemExpress. Usage Cited in: Cell Death Differ. 2023 Apr;30(4):922-937.  [Abstract]

    The interaction between MARVELD1 and PARP1 is greatly enhanced following exposure to Hydroxyurea (HU) in HeLa (8 mM HU; 24 h) and HEK293T cells (4 mM HU; 24 h).

    Hydroxyurea purchased from MedChemExpress. Usage Cited in: Signal Transduct Target Ther. 2022 Oct 17;7(1):354.  [Abstract]

    H1650 cells were treated with HA-9104 (5, 10 μM) or Hydroxyurea (HU, 5 mM) for 2 h. Chromatin proteins were isolated from whole cell lysate, followed by Western blotting.

    Hydroxyurea purchased from MedChemExpress. Usage Cited in: Nat Commun. 2022 Aug 16;13(1):4822.  [Abstract]

    SA-β-Gal assays for WT and Irf8-/- BMDMs treated with hydroxyurea (HU, 10 mM) or mitomycin C (MMC, 1µM) for 5 days. Scale bars, 200 μm.

    Hydroxyurea purchased from MedChemExpress. Usage Cited in: Nat Commun. 2022 Aug 16;13(1):4822.  [Abstract]

    qPCR analysis of the SASP genes in WT and Irf8-/- BMDMs treated with hydroxyurea (HU, 10 mM) or mitomycin C (MMC, 1 µM) for 6 days.

    DNA/RNA Synthesis アイソフォーム固有の製品をすべて表示:

    HIV アイソフォーム固有の製品をすべて表示:

    • 生物活性

    • プロトコル

    • 純度とドキュメンテーション

    • 参考文献

    • カスタマーレビュー

    製品説明

    Hydroxyurea is a cell apoptosis inducer that inhibit DNA synthesis through inhibition of ribonucleotide reductase. Hydroxyurea shows anti-orthopoxvirus activity.

    IC50 & Target

    HIV-1

     

    Cellular Effect
    Cell Line Type Value Description References
    Erythrocyte CC50
    147 3
    Compound: HU
    Cytotoxicity against human erythrocytes assessed as cell viability after 3 days alamar blue assay
    Cytotoxicity against human erythrocytes assessed as cell viability after 3 days alamar blue assay
    [PMID: 33109398]
    Erythrocyte CC50
    147 3
    Compound: HU
    Cytotoxicity against human erythrocytes assessed as cell viability after 3 days alamar blue assay
    Cytotoxicity against human erythrocytes assessed as cell viability after 3 days alamar blue assay
    [PMID: 33109398]
    HeLa S3 ED50
    1.96 6
    Compound: hydroxyurea
    Cytotoxicity against human HeLaS3 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human HeLaS3 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    HeLa S3 ED50
    1.96 6
    Compound: hydroxyurea
    Cytotoxicity against human HeLaS3 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human HeLaS3 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    K562 IC50
    687.94 3
    Compound: Hydroxyurea
    Cytotoxicity against Homo sapiens (human) K562 cells after 24 hr by MTT assay
    Cytotoxicity against Homo sapiens (human) K562 cells after 24 hr by MTT assay
    10.1007/s00044-010-9544-6
    KB ED50
    5.29 6
    Compound: hydroxyurea
    Cytotoxicity against human KB cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human KB cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    Erythrocyte CC50
    147 3
    Compound: HU
    Cytotoxicity against human erythrocytes assessed as cell viability after 3 days alamar blue assay
    Cytotoxicity against human erythrocytes assessed as cell viability after 3 days alamar blue assay
    [PMID: 33109398]
    K562 IC50
    687.94 3
    Compound: Hydroxyurea
    Cytotoxicity against Homo sapiens (human) K562 cells after 24 hr by MTT assay
    Cytotoxicity against Homo sapiens (human) K562 cells after 24 hr by MTT assay
    10.1007/s00044-010-9544-6
    HCT-116 IC50
    223 3
    Compound: Hydroxyurea
    Cytostatic activity against human HCT116 cells
    Cytostatic activity against human HCT116 cells
    [PMID: 19581098]
    L1210 ED50
    2.67 6
    Compound: hydroxyurea
    Cytotoxicity against mouse L1210 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against mouse L1210 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    KB ED50
    5.29 6
    Compound: hydroxyurea
    Cytotoxicity against human KB cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human KB cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    L1210 ED50
    2.67 6
    Compound: hydroxyurea
    Cytotoxicity against mouse L1210 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against mouse L1210 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    L1210 IC50
    82 3
    Compound: Hydroxyurea
    Activity against lymphocytic murine leukemia cell line L1210 using MTS/PES microculture tetrazolium assay
    Activity against lymphocytic murine leukemia cell line L1210 using MTS/PES microculture tetrazolium assay
    [PMID: 11784145]
    MOLT-3 ED50
    3.18 6
    Compound: hydroxyurea
    Cytotoxicity against human TMOLT3 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human TMOLT3 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    L1210 IC50
    82 3
    Compound: Hydroxyurea
    Activity against lymphocytic murine leukemia cell line L1210 using MTS/PES microculture tetrazolium assay
    Activity against lymphocytic murine leukemia cell line L1210 using MTS/PES microculture tetrazolium assay
    [PMID: 11784145]
    SW480 ED50
    4.79 6
    Compound: hydroxyurea
    Cytotoxicity against human SW480 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human SW480 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    L1210 IC50
    85 3
    Compound: Hydroxyurea
    Antiproliferative activity of compound expressed as concentration that inhibits 50% of growth of L1210 leukemic cell suspension from 24 to 48 hr after compound addition.
    Antiproliferative activity of compound expressed as concentration that inhibits 50% of growth of L1210 leukemic cell suspension from 24 to 48 hr after compound addition.
    [PMID: 2709372]
    U373-MAGI EC50
    25.8 3
    Compound: Hydroxyurea
    Potentiation of 5-Aza-C-induced antiviral activity against VSV-G pseudotyped HIV-1 NL4-3 infected in human U373-MAGI cells assessed as 5-Aza-C EC50 at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs and subsequent viral infection meas
    Potentiation of 5-Aza-C-induced antiviral activity against VSV-G pseudotyped HIV-1 NL4-3 infected in human U373-MAGI cells assessed as 5-Aza-C EC50 at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs and subsequent viral infection meas
    [PMID: 27117260]
    MOLT-3 ED50
    3.18 6
    Compound: hydroxyurea
    Cytotoxicity against human TMOLT3 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human TMOLT3 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    U373-MAGI CC50
    252 3
    Compound: Hydroxyurea
    Increase of 5-Aza-C-mediated cytotoxicity against human U373-MAGI cells at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs measured after 72 hrs by Celltiter-Glo luminescent cell viability assay (Rvb = 387 uM)
    Increase of 5-Aza-C-mediated cytotoxicity against human U373-MAGI cells at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs measured after 72 hrs by Celltiter-Glo luminescent cell viability assay (Rvb = 387 uM)
    [PMID: 27117260]
    U-937 IC50
    115 3
    Compound: Hydroxyurea
    Cytotoxicity against Homo sapiens (human) U937 cells after 96 hr by MTT assay
    Cytotoxicity against Homo sapiens (human) U937 cells after 96 hr by MTT assay
    10.1007/s00044-011-9778-y
    Vero IC50
    0.1 2
    Compound: Hydroxyurea (HU)
    Compound tested on vero cells infected with Toxoplasma gondii after 24 h
    Compound tested on vero cells infected with Toxoplasma gondii after 24 h
    [PMID: 15863319]
    Vero IC50
    0.1 2
    Compound: Hydroxyurea (HU)
    Compound tested on intracellular parasites Toxoplasma gondii in vero cells after 24 h
    Compound tested on intracellular parasites Toxoplasma gondii in vero cells after 24 h
    [PMID: 15863319]
    SW480 ED50
    4.79 6
    Compound: hydroxyurea
    Cytotoxicity against human SW480 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human SW480 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    HeLa S3 ED50
    1.96 6
    Compound: hydroxyurea
    Cytotoxicity against human HeLaS3 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human HeLaS3 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    U373-MAGI CC50
    252 3
    Compound: Hydroxyurea
    Increase of 5-Aza-C-mediated cytotoxicity against human U373-MAGI cells at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs measured after 72 hrs by Celltiter-Glo luminescent cell viability assay (Rvb = 387 uM)
    Increase of 5-Aza-C-mediated cytotoxicity against human U373-MAGI cells at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs measured after 72 hrs by Celltiter-Glo luminescent cell viability assay (Rvb = 387 uM)
    [PMID: 27117260]
    U373-MAGI EC50
    25.8 3
    Compound: Hydroxyurea
    Potentiation of 5-Aza-C-induced antiviral activity against VSV-G pseudotyped HIV-1 NL4-3 infected in human U373-MAGI cells assessed as 5-Aza-C EC50 at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs and subsequent viral infection meas
    Potentiation of 5-Aza-C-induced antiviral activity against VSV-G pseudotyped HIV-1 NL4-3 infected in human U373-MAGI cells assessed as 5-Aza-C EC50 at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs and subsequent viral infection meas
    [PMID: 27117260]
    U-937 IC50
    115 3
    Compound: Hydroxyurea
    Cytotoxicity against Homo sapiens (human) U937 cells after 96 hr by MTT assay
    Cytotoxicity against Homo sapiens (human) U937 cells after 96 hr by MTT assay
    10.1007/s00044-011-9778-y
    Vero IC50
    0.1 2
    Compound: Hydroxyurea (HU)
    Compound tested on intracellular parasites Toxoplasma gondii in vero cells after 24 h
    Compound tested on intracellular parasites Toxoplasma gondii in vero cells after 24 h
    [PMID: 15863319]
    Vero IC50
    0.5 2
    Compound: hydroxyurea
    Inhibition of Toxoplasma gondii infected in african green monkey Vero cells
    Inhibition of Toxoplasma gondii infected in african green monkey Vero cells
    [PMID: 17905587]
    Vero IC50
    1 2
    Compound: hydroxyurea
    Inhibition of uninfected african green monkey Vero cells
    Inhibition of uninfected african green monkey Vero cells
    [PMID: 17905587]
    K562 IC50
    687.94 3
    Compound: Hydroxyurea
    Cytotoxicity against Homo sapiens (human) K562 cells after 24 hr by MTT assay
    Cytotoxicity against Homo sapiens (human) K562 cells after 24 hr by MTT assay
    10.1007/s00044-010-9544-6
    KB ED50
    5.29 6
    Compound: hydroxyurea
    Cytotoxicity against human KB cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human KB cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    L1210 ED50
    2.67 6
    Compound: hydroxyurea
    Cytotoxicity against mouse L1210 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against mouse L1210 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    L1210 IC50
    82 3
    Compound: Hydroxyurea
    Activity against lymphocytic murine leukemia cell line L1210 using MTS/PES microculture tetrazolium assay
    Activity against lymphocytic murine leukemia cell line L1210 using MTS/PES microculture tetrazolium assay
    [PMID: 11784145]
    L1210 IC50
    85 3
    Compound: Hydroxyurea
    Antiproliferative activity of compound expressed as concentration that inhibits 50% of growth of L1210 leukemic cell suspension from 24 to 48 hr after compound addition.
    Antiproliferative activity of compound expressed as concentration that inhibits 50% of growth of L1210 leukemic cell suspension from 24 to 48 hr after compound addition.
    [PMID: 2709372]
    MCF7 IC50
    > 100 3
    Compound: Hydroxyurea
    Cytostatic activity against human MCF7 cells
    Cytostatic activity against human MCF7 cells
    [PMID: 19581098]
    MOLT-3 ED50
    3.18 6
    Compound: hydroxyurea
    Cytotoxicity against human TMOLT3 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human TMOLT3 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    MOLT-4 IC50
    > 100 3
    Compound: Hydroxyurea
    Cytostatic activity against human MOLT4 cells
    Cytostatic activity against human MOLT4 cells
    [PMID: 19581098]
    NCI-H460 IC50
    > 100 3
    Compound: Hydroxyurea
    Cytostatic activity against human H460 cells
    Cytostatic activity against human H460 cells
    [PMID: 19581098]
    P388 IC50
    32 3
    Compound: Hydroxyurea
    Antiproliferative activity of compound expressed as concentration that inhibits 50% of growth of P388 leukemic cell suspension from 24 to 48 hr after compound addition
    Antiproliferative activity of compound expressed as concentration that inhibits 50% of growth of P388 leukemic cell suspension from 24 to 48 hr after compound addition
    [PMID: 2709372]
    SW-620 IC50
    > 100 3
    Compound: Hydroxyurea
    Cytostatic activity against human SW620 cells
    Cytostatic activity against human SW620 cells
    [PMID: 19581098]
    SW480 ED50
    4.79 6
    Compound: hydroxyurea
    Cytotoxicity against human SW480 cells after 3 days by trypan blue exclusion technique
    Cytotoxicity against human SW480 cells after 3 days by trypan blue exclusion technique
    [PMID: 1800632]
    U-937 IC50
    115 3
    Compound: Hydroxyurea
    Cytotoxicity against Homo sapiens (human) U937 cells after 96 hr by MTT assay
    Cytotoxicity against Homo sapiens (human) U937 cells after 96 hr by MTT assay
    10.1007/s00044-011-9778-y
    U373-MAGI CC50
    252 3
    Compound: Hydroxyurea
    Increase of 5-Aza-C-mediated cytotoxicity against human U373-MAGI cells at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs measured after 72 hrs by Celltiter-Glo luminescent cell viability assay (Rvb = 387 uM)
    Increase of 5-Aza-C-mediated cytotoxicity against human U373-MAGI cells at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs measured after 72 hrs by Celltiter-Glo luminescent cell viability assay (Rvb = 387 uM)
    [PMID: 27117260]
    U373-MAGI EC50
    25.8 3
    Compound: Hydroxyurea
    Potentiation of 5-Aza-C-induced antiviral activity against VSV-G pseudotyped HIV-1 NL4-3 infected in human U373-MAGI cells assessed as 5-Aza-C EC50 at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs and subsequent viral infection meas
    Potentiation of 5-Aza-C-induced antiviral activity against VSV-G pseudotyped HIV-1 NL4-3 infected in human U373-MAGI cells assessed as 5-Aza-C EC50 at 500 uM preincubated for 2 hrs followed by 5-Aza-C addition for 2 hrs and subsequent viral infection meas
    [PMID: 27117260]
    Vero IC50
    0.1 2
    Compound: Hydroxyurea (HU)
    Compound tested on intracellular parasites Toxoplasma gondii in vero cells after 24 h
    Compound tested on intracellular parasites Toxoplasma gondii in vero cells after 24 h
    [PMID: 15863319]
    Vero IC50
    0.1 2
    Compound: Hydroxyurea (HU)
    Compound tested on vero cells infected with Toxoplasma gondii after 24 h
    Compound tested on vero cells infected with Toxoplasma gondii after 24 h
    [PMID: 15863319]
    Vero IC50
    0.5 2
    Compound: hydroxyurea
    Inhibition of Toxoplasma gondii infected in african green monkey Vero cells
    Inhibition of Toxoplasma gondii infected in african green monkey Vero cells
    [PMID: 17905587]
    Vero IC50
    1 2
    Compound: hydroxyurea
    Inhibition of uninfected african green monkey Vero cells
    Inhibition of uninfected african green monkey Vero cells
    [PMID: 17905587]
    体外実験

    Hydroxyurea is used in a number of myeloproliferative, neoplastic, HIV, and non-hematological diseases[1]. Treatment of cells in primary culture with 30 μM hydroxyurea for 96 hours significantly increases the fractional HbF content. The Gγ: Aγ-globin mRNA is induced 0.30- to 8-fold in vitro[2]. Hydroxyurea has been shown to block HIV-1 reverse transcription and/or replication in quiescent peripheral blood mononuclear cells and macrophages[3].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    体内実験

    Hydroxyurea therapy producs consistent reductions in WBC and ANC without improvement in anemia over 17 weeks. Hydroxyurea at 50mg/kg produces a reduced white blood cell count, absolute neutrophil count and no improvement in anemia compared to vehicle treated sickle cell mice[4].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    臨床実験
    分子量

    76.05

    分子式

    CH4N2O2

    CAS 番号
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    O=C(N)NO

    輸送条件

    Room temperature in continental US; may vary elsewhere.

    保管条件
    Powder -20°C 3 years
      4°C 2 years
    In solvent -80°C 6 months
      -20°C 1 month
    溶剤 & 溶解度
    体外: 

    H2O : 50 mg/mL (657.46 mM; Need ultrasonic)

    DMSO : 50 mg/mL (657.46 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 13.1492 mL 65.7462 mL 131.4924 mL
    5 mM 2.6298 mL 13.1492 mL 26.2985 mL
    10 mM 1.3149 mL 6.5746 mL 13.1492 mL
    View the 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. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

    • Molarity Calculator

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    一般には略語で表示されます:C1V1 = C2V2

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    体内:

    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.

    • Protocol 1

      Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.5 mg/mL (32.87 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.
    • Protocol 2

      Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

      Solubility: ≥ 2.5 mg/mL (32.87 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 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.

    • Protocol 1

      Add each solvent one by one:  PBS

      Solubility: 100 mg/mL (1314.92 mM); Clear solution; Need ultrasonic

    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

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    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Calculation results:
    Working solution concentration: mg/mL
    This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
    The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact MedChemExpress (MCE).
    純度とドキュメンテーション

    純度: 99.34%

    参考文献

    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. 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
    H2O / DMSO 1 mM 13.1492 mL 65.7462 mL 131.4924 mL 328.7311 mL
    5 mM 2.6298 mL 13.1492 mL 26.2985 mL 65.7462 mL
    10 mM 1.3149 mL 6.5746 mL 13.1492 mL 32.8731 mL
    15 mM 0.8766 mL 4.3831 mL 8.7662 mL 21.9154 mL
    20 mM 0.6575 mL 3.2873 mL 6.5746 mL 16.4366 mL
    25 mM 0.5260 mL 2.6298 mL 5.2597 mL 13.1492 mL
    30 mM 0.4383 mL 2.1915 mL 4.3831 mL 10.9577 mL
    40 mM 0.3287 mL 1.6437 mL 3.2873 mL 8.2183 mL
    50 mM 0.2630 mL 1.3149 mL 2.6298 mL 6.5746 mL
    60 mM 0.2192 mL 1.0958 mL 2.1915 mL 5.4789 mL
    80 mM 0.1644 mL 0.8218 mL 1.6437 mL 4.1091 mL
    100 mM 0.1315 mL 0.6575 mL 1.3149 mL 3.2873 mL

    * Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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    一般には略語で表示されます:C1V1 = C2V2

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    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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    製品名:
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