Sardomozide
Based on 9 publication(s) in Google Scholar
Sardomozide is an S-adenosylmethionine decarboxylase (SAMDC) inhibitor with an IC50 of 5 nM.
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- 純度 : 98.85%
- CAS 番号: 149400-88-4
- 分子式: C11H14N6
- 分子量:230.27
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保管条件:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
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生物活性
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化学情報
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溶剤 & 溶解度
- プロトコル
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
MedChemExpress（MCE）の使用を引用している文献 Sardomozide
More- Nature. 2026 Jul;655(8121):240-250. [Abstract]
- Cell. 2020 Jun 11;181(6):1329-1345.e24. [Abstract]
- Sci Adv. 2023 May 19;9(20):eade0718. [Abstract]
- Cell Rep. 2025 Jan 28;44(1):115123. [Abstract]
- mSystems. 2024 May 16;9(5):e0024624. [Abstract]
- Metabolomics. 2025 Jun 14;21(4):82. [Abstract]
- Preprints. 2025 May 22.
- bioRxiv. 2024 Nov 17:2024.08.24.609500. [Abstract]
- SSRN. 2024 Mar 14.
Customer Validation & Images
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Others
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Bio/Physico-chemical Assay
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RT-PCR
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Bio/Physico-chemical Assay
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Cell Proliferation/Viability Assay
生物活性
製品説明
IC50 & Target
IC50: 5 nM (SAMDC)[1]
体外実験
Sardomozide is a S-adenosylmethionine decarboxylase (SAMDC) inhibitor with an IC50 of 5 nM in cell assay. Following treatment for 48 h with 3 μM Sardomozide, intracellular SAMDC activity is reduced to 10% of control[1]. When the CHO/664 cells are grown in the presence of Sardomozide and during treatment with DENSPM, vacuole formation is not observed, and these cells are growth-inhibited and contain levels of DENSPM similar to the parental CHO cells[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
化学情報
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CAS 番号 149400-88-4
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性状 Solid
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分子量 230.27
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分子式 C11H14N6
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Color Off-white to light yellow
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SMILES
N=C(C1=CC=CC2=C1CC/C2=N\NC(N)=N)N
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別名
CGP 48664; SAM-486A
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Publications (9)
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Journal Impact Factor
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Most Recent
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Nature
2026 Jul;655(8121):240-250. PMID: 42236947 -
Cell
2020 Jun 11;181(6):1329-1345.e24. PMID: 32445698
Sardomozide purchased from MedChemExpress. Usage Cited in: Cell. 2020 Jun 11;181(6):1329-1345.e24. [Abstract]
Dose dependent Sardomozide dihydrochloride inhibition (7 days) of SAM decarboxylation (polyamine metabolism) diminishes PFA cell survival in 1% O2.
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Sci Adv
Tumor-derived semaphorin 4A improves PD-1-blocking antibody efficacy by enhancing CD8+ T cell cytotoxicity and proliferation. [Abstract]2023 May 19;9(20):eade0718. PMID: 37205755
Sardomozide purchased from MedChemExpress. Usage Cited in: Sci Adv. 2023 May 19;9(20):eade0718. [Abstract]
Percentage of IFN-γ+ and mean fluorescence intensity (MFI) of Ki-67 in CD8+ T cells after anti-CD3 antibody stimulation versus anti-CD3 antibody plus rSema4A stimulation with or without sardomozide dihydrochloride (10 μM) and eflornithine hydrochloride hydrate (500 μM).
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Cell Rep
2025 Jan 28;44(1):115123. PMID: 39932195
Sardomozide purchased from MedChemExpress. Usage Cited in: Cell Rep. 2025 Jan 28;44(1):115123. [Abstract]
Diagram of the experimental plan for Sardomozide dihydrochloride (Sardo) treatment on C2C12 myotubes.
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mSystems
Mucin alleviates colonic barrier dysfunction by promoting spermine accumulation through enhanced arginine metabolism in Limosilactobacillus mucosae. [Abstract]2024 May 16;9(5):e0024624. PMID: 38564708
Sardomozide purchased from MedChemExpress. Usage Cited in: mSystems. 2024 May 16;9(5):e0024624. [Abstract]
The concentration of putrescine, spermidine, and spermine concentrations of L. mucosae culture in the MRS broth with or without mucin and sardomozide dihydrochloride.
Sardomozide purchased from MedChemExpress. Usage Cited in: mSystems. 2024 May 16;9(5):e0024624. [Abstract]
qPCR analysis of tight-junction protein expression in LS174T cells. The letters at the top of the bar plot indicate statistically significant differences between the groups (P < 0.05). LM, normal culture supernatant; LMM, co-cultured supernatant with mucin; LMS, co-cultured supernatant with 8 µM spermine; LMMS, co-cultured supernatant with mucin and sardomozide dihydrochloride; Sper, 8 µM spermine.
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Metabolomics
SAM486A-induced inhibition of AMD1: metabolic and epigenetic implications in non-small cell lung cancer cells. [Abstract]2025 Jun 14;21(4):82. PMID: 40515967 -
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bioRxiv
2024 Nov 17:2024.08.24.609500. PMID: 39253442 -
溶剤 & 溶解度
体外:
DMSO : 16.67 mg/mL (72.39 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, 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.
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.
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
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.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 1.67 mg/mL (7.25 mM); Clear solution
This protocol yields a clear solution of ≥ 1.67 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (16.7 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: ≥ 1.67 mg/mL (7.25 mM); Clear solution
This protocol yields a clear solution of ≥ 1.67 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (16.7 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.
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.
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.
プロトコル
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
純度とドキュメンテーション
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データシート (277 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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取扱説明書 (2659 KB)
参考文献
[1]. Regenass U, et al. CGP 48664, a new S-adenosylmethionine decarboxylase inhibitor with broad spectrum antiproliferative and antitumor activity. Cancer Res. 1994 Jun 15;54(12):3210-7. [Content Brief]
[2]. Kramer DL, et al. Lysosomal sequestration of polyamine analogues in Chinese hamster ovary cells resistant to the S-adenosylmethionine decarboxylase inhibitor, CGP-48664. Cancer Res. 1998 Sep 1;58(17):3883-90. [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. 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 |
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| DMSO | 1 mM | 4.3427 mL | 21.7136 mL | 43.4273 mL | 108.5682 mL |
| 5 mM | 0.8685 mL | 4.3427 mL | 8.6855 mL | 21.7136 mL | |
| 10 mM | 0.4343 mL | 2.1714 mL | 4.3427 mL | 10.8568 mL | |
| 15 mM | 0.2895 mL | 1.4476 mL | 2.8952 mL | 7.2379 mL | |
| 20 mM | 0.2171 mL | 1.0857 mL | 2.1714 mL | 5.4284 mL | |
| 25 mM | 0.1737 mL | 0.8685 mL | 1.7371 mL | 4.3427 mL | |
| 30 mM | 0.1448 mL | 0.7238 mL | 1.4476 mL | 3.6189 mL | |
| 40 mM | 0.1086 mL | 0.5428 mL | 1.0857 mL | 2.7142 mL | |
| 50 mM | 0.0869 mL | 0.4343 mL | 0.8685 mL | 2.1714 mL | |
| 60 mM | 0.0724 mL | 0.3619 mL | 0.7238 mL | 1.8095 mL |
Sardomozide 関連分類
HY-13746 関連分類
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