Tunicamycin Mixture |
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Catalog No.GC16738
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Tunicamycin Mixture은 동종인 핵간류 항생제의 혼합물로, N-당질화를 억제하고 GlcNAc 인산전달효소(GPT)를 차단한다.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 11089-65-9
Sample solution is provided at 25 µL, 10mM.
Tunicamycin Mixture은 동종인 핵간류 항생제의 혼합물로, N-당질화를 억제하고 GlcNAc 인산전달효소(GPT)를 차단한다.
Tunicamycin Mixture은 세포 내 지방질망(ER) 스트레스를 유도하고 DNA 합성 차단 및 G1 단계 정지를 유발한다[2]. Tunicamycin Mixture은 그람양성 세균, 엑스트라셀룰로스, 진균, 곰팡이 및 바이러스를 억제하고 항암활성이 있다[3].
체외 실험에서 RAW264.7 세포에 Tunicamycin Mixture(0.5μg/ml)을 2시간 동안 사전 처리한 것은 LPS 유도된 아질산염산생산을 현저하게 감소시켰으며, iNOS와 COX-2 mRNA 및 단백질의 표현을 약화시켰다[4]. Tunicamycin Mixture(1-20μg/ml)은 24-96시간 동안 전립선 암 세포 PC-3에 대해 처리하고, 용량에 따라 세포 활성을 감소시켰으며, 단백질의 N-당질화 형성을 차단하고 내 지방질망 스트레스를 유도했다[5].
체내 실험에서 Tunicamycin Mixture(1mg/kg)을 구강 내 복용으로 주입하여 쥐에게, 간의 트리글리세라이드 축적을 현저하게 증가시켰으며 간의 혈지 단백질 비밀도를 억제하고, 혈당 수준과 간의 글루코간 함량을 감소시켰다[6]. 중성 백혈구성 천식 모델(OVALPS-OVA 쥐)에서 기도 내 투여로 Tunicamycin Mixture (2μg)을 투여함으로써, 내 지방질망 스트레스 표지와 염증성 인자 사이토카인의 단백질 표현 수준을 증가시켜, 쥐의 천식 현상이 더욱 심각해졌다[7].
References:
[1] Hsu J L, Chiang P C, Guh J H. Tunicamycin induces resistance to camptothecin and etoposide in human hepatocellular carcinoma cells: role of cell-cycle arrest and GRP78[J]. Naunyn-Schmiedeberg's archives of pharmacology, 2009, 380: 373-382.
[2] Han C, Jin L, Mei Y, et al. Endoplasmic reticulum stress inhibits cell cycle progression via induction of p27 in melanoma cells[J]. Cellular signalling, 2013, 25(1): 144-149.
[3] Pałasz A, Cież D. In search of uracil derivatives as bioactive agents. Uracils and fused uracils: Synthesis, biological activity and applications[J]. European journal of medicinal chemistry, 2015, 97: 582-611.
[4] Kim S Y, Hwang J S, Han I O. Tunicamycin inhibits Toll-like receptor-activated inflammation in RAW264. 7 cells by suppression of NF-κB and c-Jun activity via a mechanism that is independent of ER-stress and N-glycosylation[J]. European journal of pharmacology, 2013, 721(1-3): 294-300.
[5] Guha P, Kaptan E, Gade P, et al. Tunicamycin induced endoplasmic reticulum stress promotes apoptosis of prostate cancer cells by activating mTORC1[J]. Oncotarget, 2017, 8(40): 68191.
[6] Feng B, Huang X, Jiang D, et al. Endoplasmic reticulum stress inducer tunicamycin alters hepatic energy homeostasis in mice[J]. International journal of molecular sciences, 2017, 18(8): 1710.
[7]Guo Q, Li H, Liu J, et al. Tunicamycin aggravates endoplasmic reticulum stress and airway inflammation via PERK-ATF4-CHOP signaling in a murine model of neutrophilic asthma[J]. Journal of Asthma, 2017, 54(2): 125-133.
| 세포 실험[1]: | |
세포 라인 | RAW264.7 세포 |
제조 방법 | RAW264.7 세포에 0.5μg/ml의 Tunicamycin Mixture를 2시간 동안 사전 처리한 다음, LPS와 함께 18시간 동안 배양하였다. |
반응 조건 | 0.5μg/ml; 2 h |
응용 분야 | Tunicamycin Mixture은 LPS가 유도한 아질산염산의 생산/방출을 현저하게 감소시켰으며, iNOS와 COX-2 mRNA 및 단백질 표현을 완화시켰다. |
동물 실험 [2]: | |
동물 모형 | C57BL/6 수컷 쥐 |
제조 방법 | 쥐는 비슷한 평균 체중과 혈당 수준에 따라 무작위로 2 그룹으로 나뉘었다. 한 그룹은 1mg/kg Tunicamycin Mixture 또는 배달체를 구강 내 복용으로 주입받았다. 주입 후 24시간 동안 밥을 먹은 상태에서 체중과 혈당 수준을 측정했다. 그 후, 쥐는 이산화탄소를 사용하여 마취살해를 실시한 다음 자궁경부 탈구을 진행했다. |
제형 | 1mg/kg;i.p. |
응용 분야 | Tunicamycin Mixture 24시간 처리는 간의 트리글리세라이드 축적을 현저하게 증가시켰으며, 간의 혈지 단백질 비밀도를 억제하고, 혈당 수준과 간의 글루코간 함량을 감소시켰다. |
참고문헌: [1] Kim S Y, Hwang J S, Han I O. Tunicamycin은 ER 스트레스와 N-당질화에 독립적인 메커니즘을 통해 NF-κB와 c-Jun 활성을 억제하여 RAW264.7 세포에서 톨样 수용체 활성화 염증을 억제한다[J]. 유럽 약리학 저널, 2013, 721(1-3): 294-300. [2] 풍 B, 황 X, 장 D 등.내 지방질망 스트레스 유도체 튜니카마이신은 쥐 간 에너지 역학 균형을 변화시킨다[J]. 국제 분자 과학 저널, 2017, 18(8): 1710. | |
| Cas No. | 11089-65-9 | SDF | |
| Formula | C39H64N4O16 (for Tunicamycin VII) | M.Wt | 845.0 |
| Solubility | DMF: 20 mg/ml DMSO: 20 mg/ml DMSO:PBS(pH 7.2) (1:3): 0.25 mg/ml | Storage | Store at -20°C |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 1.1834 mL | 5.9172 mL | 11.8343 mL |
| 5 mM | 236.7 μL | 1.1834 mL | 2.3669 mL |
| 10 mM | 118.3 μL | 591.7 μL | 1.1834 mL |
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Related Biological Data

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The ER-stress agonist group was administered with MPs at 2.0 mg/kg.bw/d by gavage, followed by intraperitoneal injection of TM(GlpBio) at 100 mg/kg.bw/d after 30 min.
Environmental Toxicology (2024). PMID: 38440912 IF: 4.5003 -
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