GLPBio

Safranal

Catalog No.: GC60332Purity:>90.00%
Safranal은 Saffron(Crocus sativus)의 구강 활성 주성분이며 이 향신료의 독특한 향을 담당합니다.

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


Safranal
Cas No.: 116-26-7
100mgIn Stock
$15.00
1
500mgIn Stock
$46.00
1

인용 문헌 (Citations)

현재 이 제품에 대한 인용 문헌이 없습니다. 아래는 GlpBio 제품을 인용한 주요 논문입니다.
  • Nature cover
    Nature
    641, 529–536 (2025)
  • Nature cover
    Nature
    628, 630–638 (2024)
  • Nature cover
    Nature
    632, 686–694 (2024)
  • Nature cover
    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
  • Science cover
    Science
    387(6739) (2025)
  • Science cover
    Science
    387(6734) (2025)
  • Cell Research cover
    Cell Research
    35, 97–116 (2025)
  • Cell Research cover
    Cell Research
    34, 683–706 (2024)
  • Cell Research cover
    Cell Research
    33, 273–287 (2023)
  • Cell Research cover
    Cell Research
    33, 546–561 (2023)
  • Cell Research cover
    Cell Research
    33, 904–922 (2023)
  • Cell Research cover
    Cell Research
    31, 1291–1307 (2021)

제품 설명 (Description)

Safranal is a novel, orally active monoterpene aldehyde and the main active component of saffron. Safranal has neuroprotective and anti-inflammatory effects. Safranal can be used in the study of Parkinson's disease and chronic inflammation[1-4].

In vitro, Safranal (300–700μM) and VEGF (30ng/ml) were used to treat human umbilical vein endothelial cells (HUVECs) and hepatocellular carcinoma cells (HepG2) for 8–24 hours. Safranal significantly inhibited cell proliferation, migration, and tube formation, while reducing the expression of angiogenesis-related factors (such as VEGF and HIF-1α) and downstream signaling proteins[5]. Safranal (10–1000μM) was applied to treat human hepatocellular carcinoma cells (HepG2) for 24 hours. Safranal significantly inhibited cell viability and reduced cell survival rates[6].

In vivo, Safranal (100 or 200mg/kg; once daily) was administered via oral gavage to membranous glomerulonephritis (MGN) Sprague-Dawley (SD) rat models for 4 weeks. Safranal significantly reduced renal injury, inflammation, and podocyte damage in MGN rats, and improved renal function[7]. Safranal (200 or 500mg/kg; once daily) was given by gavage to ovalbumin (OVA)-induced Balb/c mouse asthma models for 7 days. Safranal significantly reduced inflammatory cell infiltration and goblet cell mucus secretion in lung tissues, decreased the number of mast cells in lung tissues, and regulated Th1/Th2 cytokine levels to alleviate asthma symptoms. One hour before antigen injection, Safranal (200 or 500mg/kg; single dose) was administered via oral gavage to passive systemic anaphylaxis (PSA) Balb/c mouse models. Safranal significantly reduced the levels of histamine and leukotriene C4 (LTC4) in the serum of PSA mice, thereby inhibiting allergic reactions[8].

References:
[1] Esmaealzadeh D, Moodi Ghalibaf A, Shariati Rad M, et al. Pharmacological effects of Safranal: An updated review. Iran J Basic Med Sci. 2023;26(10):1131-1143.
[2] Fazeli E, Ghalibaf MHE, Forouzanfar F. Neuroprotective Potency of Safranal Against Neurological Disorders. Curr Mol Med. 2023;23(9):952-959.
[3] Sheng SR, Wu YH, Dai ZH, et al. Safranal inhibits estrogen-deficiency osteoporosis by targeting Sirt1 to interfere with NF-κB acetylation. Phytomedicine. 2023 Jun;114:154739.
[4] Gupta M, Wani A, Ahsan AU, et al. Safranal inhibits NLRP3 inflammasome activation by preventing ASC oligomerization. Toxicol Appl Pharmacol. 2021 Jul 15;423:115582.
[5] Abdalla A, Murali C, Amin A. Safranal Inhibits Angiogenesis via Targeting HIF-1α/VEGF Machinery: In Vitro and Ex Vivo Insights. Front Oncol. 2022 Feb 2;11:789172.
[6] Abdalla Y, Abdalla A, Hamza AA, et al. Safranal Prevents Liver Cancer Through Inhibiting Oxidative Stress and Alleviating Inflammation. Front Pharmacol. 2022 Feb 1;12:777500.
[7] Bao Y, Ge YM, Wang Z, et al. Safranal Ameliorates Renal Damage, Inflammation, and Podocyte Injury in Membranous Nephropathy via SIRT/NF-κB Signalling. Curr Med Sci. 2025 Apr;45(2):288-300.
[8] Lertnimitphun P, Zhang W, Fu W, et al. Safranal Alleviated OVA-Induced Asthma Model and Inhibits Mast Cell Activation. Front Immunol. 2021 May 20;12:585595.

실험 프로토콜 (Protocol)

Cell experiment [1]:

Cell lines

HepG2 cells (human liver carcinoma cell line)

Preparation Method

HepG2 cells were grown in RPMI 1640 medium supplemented with 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin at 37°C in a humidified 5% CO₂ atmosphere. HepG2 cells were seeded in 96-well plates, allowed to attach for 24 hours, incubated in serum-free medium for at least 12 hours, and then treated with various concentrations of Safranal (10-1000μM) for specified durations.

Reaction Conditions

10-1000μM; 24-48h

Applications

Safranal exhibited a significant dose-dependent reduction of HepG2 cell viability. Safranal significantly increased caspase-3 and -7 activities, induced DNA double-strand breaks (assessed by phosphorylation of histone H2X), and significantly decreased IL-8 (CXCL8) secretion levels.

Animal experiment [2]:

Animal models

Sprague-Dawley (SD) rats

Preparation Method

Rats were immunized with cationic bovine serum albumin (C-BSA) to establish the membranous nephropathy (MGN) model. After successful model establishment, rats were administered Safranal by oral gavage for 4 consecutive weeks.

Dosage form

100 or 200mg/kg; p.o. (oral gavage); once daily for 4 weeks

Applications

Safranal administration significantly reduced kidney weight and the kidney somatic index in MGN rats. Safranal improved renal dysfunction by decreasing urine protein levels, increasing serum albumin levels, and regulating the levels of blood urea nitrogen, serum creatinine, total cholesterol, and triglycerides. Additionally, Safranal mitigated histological changes (reducing glomerular expansion and inflammatory cell infiltration), decreased the deposition of IgG and C3 in kidney tissues, alleviated podocyte injury (upregulating the expression of podocin, nephrin, and WT-1), and inhibited renal inflammation by activating Sirt1 and inhibiting NF-κB signaling pathway.

References:
[1] Abdalla Y, Abdalla A, Hamza AA, et al. Safranal Prevents Liver Cancer Through Inhibiting Oxidative Stress and Alleviating Inflammation. Front Pharmacol. 2022 Feb 1;12:777500.
[2] Bao Y, Ge YM, Wang Z, et al. Safranal Ameliorates Renal Damage, Inflammation, and Podocyte Injury in Membranous Nephropathy via SIRT/NF-κB Signalling. Curr Med Sci. 2025 Apr;45(2):288-300.

제품 문서 (Product Documents)

Purity:>90.00%Appearance:A liquid

화학적 특성 (Chemical Properties)

CAS 번호
116-26-7
SMILES
O=CC1=C(C)C=CCC1(C)C
분자식
C10H14O
분자량
150.22
용해도
DMF: 30 mg/ml,DMSO: 30 mg/ml
보관
Store at -20°C, stored under nitrogen
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

Reviews

Review for Safranal

Rating: 5
  • 5 Star100%
  • 4 Star0%
  • 3 Star0%
  • 2 Star0%
  • 1 Star0%