1. Apoptosis
  2. MDM-2/p53
  3. Triglycidyl isocyanurate

Triglycidyl isocyanurate (Synonyms: TGIC; Teroxirone)

Cat. No.: HY-W011434
Handling Instructions

Triglycidyl isocyanurate (TGIC; Teroxirone) is a triazene triepoxide with antiangiogenic and antineoplastic activities. Triglycidyl isocyanurate inhibits the growth of non-small-cell-lung cancer cells via p53 activation. Triglycidyl isocyanurate induces cell apoptosis. Triglycidyl isocyanurate can be used for cancer research.

For research use only. We do not sell to patients.

Triglycidyl isocyanurate Chemical Structure

Triglycidyl isocyanurate Chemical Structure

CAS No. : 2451-62-9

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Based on 1 publication(s) in Google Scholar

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Description

Triglycidyl isocyanurate (TGIC; Teroxirone) is a triazene triepoxide with antiangiogenic and antineoplastic activities. Triglycidyl isocyanurate inhibits the growth of non-small-cell-lung cancer cells via p53 activation. Triglycidyl isocyanurate induces cell apoptosis. Triglycidyl isocyanurate can be used for cancer research[1][2].

In Vitro

Triglycidyl isocyanurate (0-30 μM; 48 hours) reduces the growth of spheroids of human non-small-cell-lung cancer cells in culture, it leads to a gradual reduction in size for tumorspheres of A549, H460 and H1299 cells[1].
Triglycidyl isocyanurate (0-30 μM; 48 hours) inhibits expression of akt1/2/3 and phosphorylated Aktser473/474/472 of A549, H460 and H1299 tumorspheres, however, the cleavage of PARP and procaspase-3 plus the emergent active caspase-3 fragment are only visible in H460 and A549 tumorspheres[1].

Cell Viability Assay[1]

Cell Line: A549, H460 and H1299 cells
Concentration: 0 μM; 5 μM; 10 μM; 30 μM
Incubation Time: 48 hours
Result: Inhibited tumor cells growth in soft agar.

Western Blot Analysis[1]

Cell Line: A549, H460 and H1299 cells
Concentration: 0 μM; 5 μM; 10 μM; 30 μM
Incubation Time: 48 hours
Result: Inhibited akt1/2/3 expression and p-aktser473/474/472 expression of A549, H460 and H1299 tumorspheres
In Vivo

Triglycidyl isocyanurate (subcutaneous injection; 1.8 and 3.6 mg/kg; every 2–3 days for total seven times; 30 days) suppresses the growth of xenograft tumors and has no effects on weight in nude mice[2].

Animal Model: Female nu/nu mice with Huh7 cells subcutaneously injected into the dorsal area[2]
Dosage: 1.8 mg/kg and 3.6 mg/kg
Administration: Subcutaneous injection; every 2–3 days for total seven times; 30 days
Result: Inhibited the growth of xenograft tumors.
Molecular Weight

297.26

Formula

C₁₂H₁₅N₃O₆

CAS No.

2451-62-9

SMILES

O=C(N(C1=O)CC2CO2)N(C(N1CC3CO3)=O)CC4CO4

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Solvent & Solubility
In Vitro: 

DMSO : 50 mg/mL (168.20 mM; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 3.3641 mL 16.8203 mL 33.6406 mL
5 mM 0.6728 mL 3.3641 mL 6.7281 mL
10 mM 0.3364 mL 1.6820 mL 3.3641 mL
*Please refer to the solubility information to select the appropriate solvent.
References
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Keywords:

Triglycidyl isocyanurateTGICTeroxironeMDM-2/p53anticancer agentNSCLChepatocellularcarcinomaHCCtumorHepG2Hep3Bliver cancerInhibitorinhibitorinhibit

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Triglycidyl isocyanurate
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