GLPBio

Cynaropicrin

Catalog No.: GC33330Purity:>98.00%
시나로피크린은 쥐와 인간 대식세포에 대해 각각 8.24 및 3.18μM의 IC50으로 종양 괴사 인자(TNF-α) 방출을 억제할 수 있는 세스퀴테르펜 락톤입니다. Cynaropicrin은 또한 연골 분해 인자(MMP13)의 증가를 억제하고 NF-κB 신호를 억제합니다.

제품은 연구용으로만 사용됩니다. 인체에 사용할 수 없으며 환자에게 판매하지 않습니다.


Cynaropicrin
Cas No.: 35730-78-0
10mM (in 1mL DMSO)In Stock
$104.00
1
1mgIn Stock
$38.00
1
5mgIn Stock
$94.00
1
10mgIn Stock
$152.00
1

인용 문헌 (Citations)

현재 이 제품에 대한 인용 문헌이 없습니다. 아래는 GlpBio 제품을 인용한 주요 논문입니다.
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제품 설명 (Description)

Cynaropicrin is a sesquiterpene lactone containing an α-methylene-γ-butyrolactone active group, isolated from the Ranunculaceae plant Saussurea lappa. Cynaropicrin has an inhibitory effect on tumor necrosis factor (TNF-α) production and cytokine-induced neutrophil chemokine-1. Cynaropicrin also inhibits the upregulation of the cartilage degradation factor MMP13 and can suppress the NF-κB signaling pathway[1][2].

In vitro, Cynaropicrin (0-40µM; 6h) exhibited no cytotoxicity in RAW264.7 and U937 cells. Cynaropicrin (0-40µM; 24h) inhibited macrophage proliferation in a dose-dependent manner, with IC₅₀ values of 16.3µM in RAW264.7 cells and 17.2µM in U937 cells. Cynaropicrin (0-40µM) inhibited the proliferation of Sup-T1 cells after 24h and 48h of treatment, with IC₅₀ values of 27.5µM and 14.1µM, respectively. Cynaropicrin (0-40µM; 6h) strongly inhibited lipopolysaccharide-induced TNF-α release from both murine and human macrophage cells in a dose-dependent manner with the IC50 values of 8.24 and 3.18µM[1]. Cynaropicrin (1–4µM; 1h) dose-dependently inhibited TNF-α-induced upregulation of MMP13, HIF-2α, and ADAMTS4 mRNA expression and reversed the downregulation of Sox9 mRNA expression in OUMS-27 cells[2].

In vivo, Cynaropicrin (2.5 and 5mg/kg; i.p.; every 2 days for 14 days) decreased tumor volume and weight in mice bearing HCT116 xenografts with minimal toxicity[3].

References:
[1] Cho, J Y et al. “In vitro anti-inflammatory effects of cynaropicrin, a sesquiterpene lactone, from Saussurea lappa.” European journal of pharmacology vol. 398,3 (2000): 399-407.
[2] Masutani, Teruaki et al. “Cynaropicrin is dual regulator for both degradation factors and synthesis factors in the cartilage metabolism.” Life sciences vol. 158 (2016): 70-7.
[3] Zheng, Dandan et al. “Cynaropicrin Shows Antitumor Progression Potential in Colorectal Cancer Through Mediation of the LIFR/STATs Axis.” Frontiers in cell and developmental biology vol. 8 605184. 11 Jan. 2021.

실험 프로토콜 (Protocol)

Cell experiment [1]:

Cell lines

RAW264.7 cells

Preparation Method

Cynaropicrin was solubilized with vehicle (89.9% propylene glycol, 10% ethanol and 0.1% dimethyl sulfoxide) were diluted with RPMI1640. The final concentration of vehicle was never exceeded 0.05% in the culture medium. Before stimulation with lipopolysaccharide (1µg/ml), RAW264.7 cells were incubated for 18h in 24 well plates under the same conditions. Stimuli and the various concentrations of Cynaropicrin were then added to the wells for 6h. Supernatants were then collected and assayed for TNF-α content.

Reaction Conditions

0-40µM;6h

Applications

Cynaropicrin (0-40µM; 6h) strongly inhibited lipopolysaccharide-induced TNF-α release in a dose-dependent manner.
Animal experiment [2]:

Animal models

Xenograft mice models bearing HCT116 cells

Preparation Method

HCT116 cells mixed with an equal volume of PBS and matrigel were implanted in the hind flank of mice (nude mice, female, 5-6 weeks old). Upon attaining an appropriate tumor volume (approximately one-week post-implantation), mice were intraperitoneally injected with Napabucasin (NAPA) or Cynaropicrin (2.5 and 5mg/kg) for 14 days. The mice were given the drug every 2 days and their weight was weighed.

Dosage form

2.5 and 5mg/kg; i.p.; every 2 days for 14 days

Applications

Intraperitoneal administration of Cynaropicrin at doses of 2.5 and 5mg/kg resulted in decreased tumor volume and weight compared to the vehicle group and Napabucasin (10mg/kg) group. LIFR and STAT3 phosphorylation was mechanistically inhibited in the treatment groups.

References:
[1] Cho, J Y et al. “In vitro anti-inflammatory effects of cynaropicrin, a sesquiterpene lactone, from Saussurea lappa.” European journal of pharmacology vol. 398,3 (2000): 399-407.
[2] Zheng, Dandan et al. “Cynaropicrin Shows Antitumor Progression Potential in Colorectal Cancer Through Mediation of the LIFR/STATs Axis.” Frontiers in cell and developmental biology vol. 8 605184. 11 Jan. 2021.

제품 문서 (Product Documents)

Purity:>98.00%Appearance:An oil

화학적 특성 (Chemical Properties)

CAS 번호
35730-78-0
SMILES
C=C([C@H]1O)[C@]([C@@]2([H])C1)([H])[C@](OC3=O)([H])[C@@](C3=C)([H])[C@@H](OC(C(CO)=C)=O)CC2=C
분자식
C19H22O6
분자량
346.37
용해도
DMSO: ≥ 50 mg/mL (144.35 mM)
보관
-20°C, protect from light
일반 주의사항
제품의 용해도 데이터에 따라 적절한 용매를 선택하십시오. 조제 후에는 반복적인 동결·해동을 피할 수 있도록 저장 용액을 소분하십시오.
저장 용액은 -80°C 보관 시 6개월 이내, -20°C 보관 시 1개월 이내에 사용하십시오.
용해도를 높이려면 튜브를 37°C로 데운 뒤 적절한 시간 동안 초음파 처리하십시오.
배송 조건
평가용 샘플은 아이스팩과 함께 배송됩니다. 그 외 용량은 실온 배송되며, 요청 시 아이스팩과 함께 배송할 수 있습니다.

계산 도구 (Calculators)몰 농도 / 희석 / 분자량 / 단위 변환 / 생체 내 제형 / 용해도

g/mol

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