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Saccharin 1-methylimidazole 482333-74-4

Saccharin 1-methylimidazole 482333-74-4

CAS No.: 482333-74-4

Saccharin 1-methylimidazole is an activator of DNA/RNA Synthesis.
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This product is for research use only, not for human use. We do not sell to patients.

Saccharin 1-methylimidazole is an activator of DNA/RNA Synthesis.

Physicochemical Properties


Molecular Formula C11H11N3O3S
Molecular Weight 265.29
Exact Mass 265.052
CAS # 482333-74-4
PubChem CID 9813926
Appearance Light yellow to orange solid powder
LogP 0.887
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 0
Heavy Atom Count 18
Complexity 348
Defined Atom Stereocenter Count 0
SMILES

O=S1(NC(=O)C2C=CC=CC1=2)=O.CN1C=NC=C1

InChi Key DMSNKRPEUQVMNF-UHFFFAOYSA-N
InChi Code

InChI=1S/C7H5NO3S.C4H6N2/c9-7-5-3-1-2-4-6(5)12(10,11)8-7;1-6-3-2-5-4-6/h1-4H,(H,8,9);2-4H,1H3
Chemical Name

1,1-dioxo-1,2-benzothiazol-3-one;1-methylimidazole
HS Tariff Code 2934.99.9001
Storage

Powder-20°C 3 years

4°C 2 years

In solvent -80°C 6 months

-20°C 1 month

Shipping Condition Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

Biological Activity


ln Vitro Calcium-deficient T51B cells are stimulated to initiate DNA synthesis rapidly, efficiently, or almost efficiently upon exposure to concentrations of the disparate promoters phenobarbital and the calcium and sodium salts of saccharin (22, 23, 25, 29, 38). This results in an increase in the extracellular calcium concentration to 1.25 mM[1].
References [1]. Boynton AL, et al. Stimulation of DNA synthesis in calcium-deprived T51B liver cells by the tumor promoters phenobarbital, saccharin, and 12-O-tetradecanoylphorbol-13-acetate. Cancer Res. 1980 Dec;40(12):4541-5.

Solubility Data


Solubility (In Vitro) DMSO : ~100 mg/mL (~376.95 mM)
H2O : ≥ 100 mg/mL (~376.95 mM)
Solubility (In Vivo) Solubility in Formulation 1: ≥ 2.5 mg/mL (9.42 mM) (saturation unknown) in 10% DMSO + 40% PEG300 + 5% Tween80 + 45% Saline (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 400 μL PEG300 and mix evenly; then add 50 μL Tween-80 to the above solution and mix evenly; then add 450 μL normal saline to adjust the volume to 1 mL.
Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH₂ O to obtain a clear solution.

Solubility in Formulation 2: ≥ 2.5 mg/mL (9.42 mM) (saturation unknown) in 10% DMSO + 90% (20% SBE-β-CD in Saline) (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of 20% SBE-β-CD physiological saline solution and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.

Solubility in Formulation 3: ≥ 2.5 mg/mL (9.42 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of 25.0 mg/mL clear DMSO stock solution to 900 μL of corn oil and mix evenly.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 3.7695 mL 18.8473 mL 37.6946 mL
5 mM 0.7539 mL 3.7695 mL 7.5389 mL
10 mM 0.3769 mL 1.8847 mL 3.7695 mL
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.