Structure of Tirapazamine
CAS No.: 27314-97-2
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Tirapazamine is an experimental anticancer drug that is activated to a toxic radical only at very low levels of oxygen.
Synonyms: Tirazone; Win59075; 3-Amino-1,2,4-benzotriazine 1,4-Dioxide
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Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
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CAS No. : | 27314-97-2 |
Formula : | C7H6N4O2 |
M.W : | 178.15 |
SMILES Code : | NC1=[N+]([O-])C2=CC=CC=C2[N+]([O-])=N1 |
Synonyms : |
Tirazone; Win59075; 3-Amino-1,2,4-benzotriazine 1,4-Dioxide
|
MDL No. : | MFCD00132954 |
InChI Key : | ORYDPOVDJJZGHQ-UHFFFAOYSA-N |
Pubchem ID : | 135413511 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
UV41 Chinese hamster ovary cells | 6 µM | 1 hour | Evaluate the cell-killing effect of TPZ combined with cisplatin, showing no enhancement of cisplatin toxicity by TPZ in ERCC4-deficient UV41 cells | Br J Cancer. 1999 Jun;80(8):1245-51 |
AA8 Chinese hamster ovary cells | 18 µM | 1 hour | Evaluate the cell-killing effect of TPZ combined with cisplatin, showing that TPZ pretreatment under hypoxia significantly enhances cisplatin cytotoxicity | Br J Cancer. 1999 Jun;80(8):1245-51 |
LXFL 529 human non-small-cell lung cancer cells | 20 µM | 1 hour | Evaluate the cell-killing effect of TPZ combined with cisplatin, showing that TPZ pretreatment under hypoxia significantly enhances cisplatin cytotoxicity | Br J Cancer. 1999 Jun;80(8):1245-51 |
NIH 3T3 mouse fibroblast cells | 20 µM | 1 hour | Evaluate the cell-killing effect of TPZ combined with cisplatin, showing that TPZ pretreatment under hypoxia significantly enhances cisplatin cytotoxicity | Br J Cancer. 1999 Jun;80(8):1245-51 |
CT26 mouse colon carcinoma cells | 0 to 200 µg/mL | 24 hours | To evaluate the toxicity of TCuH NPs on CT26 cells, results showed that the cell viability was approximately 31.2% in the TCuH + 1064 nm laser irradiation group. | J Nanobiotechnology. 2024 Apr 24;22(1):205 |
1205 Lu P cells | 20 mM | 24 hours | Compare the response of normal keratinocytes and melanoma cells expressing different connexins to NTP + TPZ treatment | Cells. 2023 Aug 21;12(16):2113 |
B16-F10 cells | 27.95 mM (TPZ alone) and 17.44 mM (NTP + TPZ) | 24 hours | Determine the IC50 of TPZ under hypoxic conditions and demonstrate the synergistic effect of NTP and TPZ combination therapy | Cells. 2023 Aug 21;12(16):2113 |
143B cells | 40 µg/mL | 3 hours | Evaluate cell viability and apoptosis, results showed that TPZ/PFA@UiO-66@PDA significantly enhanced hypoxia, induced cell apoptosis in vitro through the oxygen-dependent HIF-1α pathway. | J Nanobiotechnology. 2021 Sep 30;19(1):298 |
A549 wild type cells | 10, 25, 50, 100 µM | 6 monthourss | To evaluate the biochemical consequences of chronic aerobic tirapazamine exposure, it was found that cells developed significant aerobic resistance to TPZ, with elevated MnSOD levels and reduced DT-diaphorase and P450R activity. | Br J Cancer. 2000 Feb;82(3):651-6 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
BALB/c mice | 4T1 breast cancer model | Tail vein injection | 1 mg/kg (TPZ), 3 mg/kg (BMS) | Every 3 days, total of 4 times | Evaluate the anti-tumor efficacy of PEI-FA@IR@TPZ/BMS LPs in the 4T1 breast cancer model. Results showed that PEI-FA@IR@TPZ/BMS LPs significantly inhibited tumor growth and reduced lung metastatic nodules. Additionally, the nanoplatform enhanced immune responses, as evidenced by increased CD4+ and CD8+ T cells and decreased Tregs. | J Nanobiotechnology. 2024 Sep 12;22(1):558. |
BALB/c nude mice | Subcutaneous 143B tumor model | Tail vein injection | 10 mg/kg | Injected on days 0, 4, and 8, lasting for 16 days | Evaluate the anti-tumor effect of TPZ/PFA@UiO-66@PDA in vivo, results showed that nanoparticles accumulated in the tumor region and effectively inhibited tumor growth. | J Nanobiotechnology. 2021 Sep 30;19(1):298 |
Nude mice | HRT18 and Nal1+ xenografted tumors | Intraperitoneal injection | 144 mg/kg | Four consecutive days | To evaluate the toxicity and activity of tirapazamine alone or combined with chemotherapeutic agents. Results showed that tirapazamine combined with bleomycin or VP16 significantly increased tumor regrowth delay and cytotoxicity. | Br J Cancer. 1996 Jun;73(12):1480-5 |
BALB/c nude mice | 4T1 breast cancer model | Intravenous injection | 2 mg/kg | Administered on days 1, 4, 7, 10, 13, and 16, lasting for 16 days | Evaluate the antitumor effect of GPPCT nanoplatforms in vivo. Results showed that GPPCT specifically accumulates at tumor sites, effectively inhibits tumor growth and metastasis through the combination of CDT and chemotherapy, with no systemic toxicity | J Nanobiotechnology. 2022 Jan 21;20(1):43 |
C57BL/6 mice | B16-F10 melanoma model | Intratumoral injection | 20 μM TPZ | 5 treatments in total, every 2-3 days | Evaluate the inhibitory effect of NTP + TPZ combination therapy on melanoma growth, showing significant reduction in tumor volume and increased tumor cell death and necrosis | Cells. 2023 Aug 21;12(16):2113 |
BDF and C3H mice | T50/80 mammary carcinoma, SCCVII and RIF-1 tumour models | Intraperitoneal injection | 25-50 mg/kg | Single dose, varying from 30 minutes to 24 hours | To evaluate the anti-tumour effect and toxicity to normal bone marrow of tirapazamine in combination with cyclophosphamide. Results showed that tirapazamine at 25 mg/kg combined with cyclophosphamide (100 mg/kg) produced an anti-tumour effect equivalent to a single 150 mg/kg dose of cyclophosphamide alone. However, tirapazamine significantly increased toxicity to bone marrow cells. | Br J Cancer. 2000 Apr;82(8):1469-73 |
HBx transgenic mice | Spontaneous HCC model in HBx transgenic mice | Tail vein injection | 3 mg/kg | Single dose, followed for up to 7 days | To evaluate the efficacy of TPZ combined with hepatic artery ligation (HAL), results showed nearly complete necrosis (~99%) of HCC. | Proc Natl Acad Sci U S A. 2016 Oct 18;113(42):11937-11942 |
BALB/c nude mice | Subcutaneous colon cancer model | Tail vein injection | 5 mg/kg | Once every other day for five total treatments | To evaluate the antitumor efficacy of TCuH NPs in vivo, results showed that the tumor inhibition rate in the TCuH + 1064 nm laser group was 92.3%. | J Nanobiotechnology. 2024 Apr 24;22(1):205 |
C57BL/6 mice | RM-1 tumor model | Implantation | 5 μg/g | Single implantation, lasting 10 days | To evaluate the inhibitory effect of CA4P@S-TPZ@F-CA4P@S on postoperative tumor recurrence and metastasis, showing effective inhibition of tumor recurrence and metastasis. | Adv Sci (Weinh). 2023 Aug;10(22):e2300899 |
Bio Calculators | ||||
Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
5.61mL 1.12mL 0.56mL |
28.07mL 5.61mL 2.81mL |
56.13mL 11.23mL 5.61mL |
Tags: Tirapazamine | SR259075 | SR4233 | Win59075 | SML 0552 | SR 259075 | Tirazone | SR 259075 | SR-259075 | SR4233 | SR 4233 | SR-4233 | Win59075 | Win 59075 | Win-59075 | SML0552 | SML 0552 | SML-0552 | DNA/RNA Synthesis | Bioreductive Agent | Anticancer Agent | inhibitor | 27314-97-2 |
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Health hazards | |
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H301 | Toxic if swallowed |
H302 | Harmful if swallowed |
H303 | May be harmful if swallowed |
H304 | May be fatal if swallowed and enters airways |
H305 | May be harmful if swallowed and enters airways |
H310 | Fatal in contact with skin |
H311 | Toxic in contact with skin |
H312 | Harmful in contact with skin |
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H314 | Causes severe skin burns and eye damage |
H315 | Causes skin irritation |
H316 | Causes mild skin irritation |
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H318 | Causes serious eye damage |
H319 | Causes serious eye irritation |
H320 | Causes eye irritation |
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H331 | Toxic if inhaled |
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H333 | May be harmful if inhaled |
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H336 | May cause drowsiness or dizziness |
H340 | May cause genetic defects |
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H350 | May cause cancer |
H351 | Suspected of causing cancer |
H360 | May damage fertility or the unborn child |
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H361d | Suspected of damaging the unborn child |
H362 | May cause harm to breast-fed children |
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H372 | Causes damage to organs through prolonged or repeated exposure |
H373 | May cause damage to organs through prolonged or repeated exposure |
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Code | Phrase |
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H401 | Toxic to aquatic life |
H402 | Harmful to aquatic life |
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H411 | Toxic to aquatic life with long-lasting effects |
H412 | Harmful to aquatic life with long-lasting effects |
H413 | May cause long-lasting harmful effects to aquatic life |
H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
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