1. Cell Cycle/DNA Damage
  2. G-quadruplex
  3. Pyridostatin

Pyridostatin (RR82) is a G-quadruplex DNA stabilizing agent (Kd=490 nM) and can target DNA and RNA G4s in cells. Pyridostatin promotes growth arrest in human cancer cells by inducing replication- and transcription-dependent DNA damage. Pyridostatin targets the proto-oncogene Src. Pyridostatin reduced SRC protein levels and SRC-dependent cellular motility in human breast cancer cells.

The free form of the compound is prone to instability, it is advisable to consider the stable salt form that retains the same biological activity.

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CAS No. : 1085412-37-8

사이즈 가격 재고
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Other Forms of Pyridostatin:

Top Publications Citing Use of Products

34 Publications Citing Use of MCE Pyridostatin

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

    Pyridostatin purchased from MedChemExpress. Usage Cited in: Nat Commun. 2022 Sep 16;13(1):5456.  [Abstract]

    Stacked bar graphs of zebrafish embryos in dead, deformd, and normal status with different G4 stabilizer (Pyridostatin hydrochloride, 0.05-20 ng/μL, 5 nL) concentration at 24 hpf (d) and 48 hpf (e).

    Pyridostatin purchased from MedChemExpress. Usage Cited in: Nat Commun. 2022 Sep 16;13(1):5456.  [Abstract]

    qRT-PCR measurement of shox. The mRNA expression level of the shoxgene was detected at different time points (3, 7, and 14 days post-fertilization; i.e., 3 dpf, 7 dpf, and 14 dpf). The results showed that, compared with wild-type zebrafish, the G4 stabilizer Pyridostatin hydrochloride (0.05-0.1 ng/μL) significantly reduced the shox mRNA expression level in wrn−/− zebrafish.

    Pyridostatin purchased from MedChemExpress. Usage Cited in: J Hepatol. 2020 Aug;73(2):371-382.  [Abstract]

    Levels of miR-26a in MPHs transfected with miR-26a-WT or miR-26a-G4mut plasmids and stimulated with Pyridostatin hydrochloride (PDS, 10 μM; 48 h). The results showed that PDS significantly diminished the increase in miR-26a expression induced by miR-26a-WT plasmids, but not by miR-26a-G4mut plasmids, indicating that the G/A mutations are sufficient to abolish the inhibitory effect of PDS on miR-26a expression.

    Pyridostatin purchased from MedChemExpress. Usage Cited in: J Hepatol. 2020 Aug;73(2):371-382.  [Abstract]

    Pyridostatin hydrochloride (PDS, 10 μM; 48 h) markedly inhibited insulin-induced AKT activation, a central hallmark of insulin sensitivity, in MPHs (isolated from C57BL/6 mice) transfected with miR-26a-WT plasmids.

    Pyridostatin purchased from MedChemExpress. Usage Cited in: J Hepatol. 2020 Aug;73(2):371-382.  [Abstract]

    8- to 10-week-old mice were infused with Pyridostatin hydrochloride (PDS, 6 mg/kg body weight) or saline (NC) via caudal vein twice a day (n = 5). 12 h post the second injection, the following measurements were performed. Representative H&E staining of paraffin liver sections. Scale bars: 20 μm. The results showed that no significant differences in histology and morphology were observed between PDS-treated mice and saline-treated mice.
    • Biological Activity

    • 순도&문서

    • References

    • 고객리뷰

    제품 설명

    Pyridostatin (RR82) is a G-quadruplex DNA stabilizing agent (Kd=490 nM) and can target DNA and RNA G4s in cells. Pyridostatin promotes growth arrest in human cancer cells by inducing replication- and transcription-dependent DNA damage. Pyridostatin targets the proto-oncogene Src. Pyridostatin reduced SRC protein levels and SRC-dependent cellular motility in human breast cancer cells[1][2].

    IC50 & Target

    Kd: 490 nM (G-quadruplexe)[1]

    Cellular Effect
    Cell Line Type Value Description References
    MRC5 IC50
    5.38 μM
    Compound: Pyridostatin
    Cytotoxicity against human MRC5 cells assessed as cell growth inhibition after 72 hrs by MTT assay
    Cytotoxicity against human MRC5 cells assessed as cell growth inhibition after 72 hrs by MTT assay
    [PMID: 29323491]
    MRC5 IC50
    5.4 μM
    Compound: PDS
    Cytotoxicity against human MRC5 cells
    Cytotoxicity against human MRC5 cells
    [PMID: 38971047]
    In Vitro

    Pyridostatin (RR82) (10 μM; 48 hours) induces cell cycle arrest[1].
    Pyridostatin is a very selective G-quadruplex DNA-binding small molecule designed to form a complex with and stabilize G-quadruplex structure. Pyridostatin causes neurite retraction, synaptic loss, and dose-dependent neuronal death. In cultured primary neurons, Pyridostatin induces the formation of DNA DSBs. Remarkably, Pyridostatin (1-5 μM, overnight) downregulates the BRCA1 protein, a protein that guards and repairs the neuronal genome, at the transcriptional level[3].

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

    Cell Viability Assay[1]

    Cell Line: Over 60 different cancer cell lines
    Concentration: 10 μM
    Incubation Time: 48 hours
    Result: Predominantly accumulated in the G2 phase of the cell cycle over 60 different cancer cell lines.
    분자량

    596.64

    화학식

    C31H32N8O5

    CAS No.
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    O=C(C1=CC(OCCN)=CC(C(NC2=NC3=C(C(OCCN)=C2)C=CC=C3)=O)=N1)NC4=CC(OCCN)=C5C=CC=CC5=N4

    선적

    Room temperature in continental US; may vary elsewhere.

    보관
    Powder -20°C 3 years
    In solvent -80°C 6 months
    -20°C 1 month
    용액&용해도
    In Vitro: 

    DMSO : ≥ 100 mg/mL (167.61 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    *"≥" means soluble, but saturation unknown.

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 1.6761 mL 8.3803 mL 16.7605 mL
    5 mM 0.3352 mL 1.6761 mL 3.3521 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.

    • 몰농도 계산기

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    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    Concentration (start)

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    In Vivo Dissolution Calculator
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    순도&문서
    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, 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
    DMSO 1 mM 1.6761 mL 8.3803 mL 16.7605 mL 41.9013 mL
    5 mM 0.3352 mL 1.6761 mL 3.3521 mL 8.3803 mL
    10 mM 0.1676 mL 0.8380 mL 1.6761 mL 4.1901 mL
    15 mM 0.1117 mL 0.5587 mL 1.1174 mL 2.7934 mL
    20 mM 0.0838 mL 0.4190 mL 0.8380 mL 2.0951 mL
    25 mM 0.0670 mL 0.3352 mL 0.6704 mL 1.6761 mL
    30 mM 0.0559 mL 0.2793 mL 0.5587 mL 1.3967 mL
    40 mM 0.0419 mL 0.2095 mL 0.4190 mL 1.0475 mL
    50 mM 0.0335 mL 0.1676 mL 0.3352 mL 0.8380 mL
    60 mM 0.0279 mL 0.1397 mL 0.2793 mL 0.6984 mL
    80 mM 0.0210 mL 0.1048 mL 0.2095 mL 0.5238 mL
    100 mM 0.0168 mL 0.0838 mL 0.1676 mL 0.4190 mL
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      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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    Inquiry Information

    상품명:
    Pyridostatin
    Cat. No.:
    HY-15176
    수량:
    MCE Japan Authorized Agent: