GLPBio

Cryptotanshinone

Catalog No.: GN10501Purity:>99.50%
Cryptotanshinone is a natural compound extracted from the roots of Salvia miltiorrhiza Bunge, exhibiting antitumor activity by inhibiting Signal Transducer and Activator of Transcription 3 (STAT3) with an IC50 value of 4.6μM.

المنتجات مخصصة للاستخدام البحثي فقط، وليست للاستخدام البشري. نحن لا نبيع للمرضى.


Cryptotanshinone
Cas No.: 35825-57-1
20mgIn Stock
$58.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
  • 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)

الوصف (Description)

Cryptotanshinone is a natural compound extracted from the roots of Salvia miltiorrhiza Bunge, exhibiting antitumor activity by inhibiting Signal Transducer and Activator of Transcription 3 (STAT3) with an IC50 value of 4.6μM[1, 2]. Cryptotanshinone possesses multiple biological activities, including antitumor, anti-inflammatory, anti-fibrotic, and anti-angiogenic effects[3, 4].

In vitro, Cryptotanshinone (20μM) treatment of A549 cells for 24h reduced the percentage of cells in the G0/G1 phase, increased the percentage of cells in the G2/M phase, induced G2/M phase arrest, and promoted apoptosis along with the expression of apoptotic genes[5]. In another study, pretreatment of H9C2 cells with Cryptotanshinone (3μM) for 1h significantly prevented chronic hypoxia-induced cell injury, restored cellular ATP levels, reduced mitochondrial superoxide levels, and decreased intracellular NO and calcium levels[6].

In vivo, Cryptotanshinone (50mg/kg/day) administered via gastric gavage for 4 weeks in a mouse model of cardiac remodeling induced by aortic banding (AB) surgery improved pressure overload-induced cardiac dysfunction, attenuated cardiac hypertrophy, and reduced cardiac fibrosis[7]. Additionally, Cryptotanshinone (40mg/kg/day) administered orally in a CCl4-induced liver fibrosis mouse model ameliorated liver fibrosis, inhibited the activation of hepatic stellate cells, and suppressed collagen production[8].

References:
[1] Zheng J, Zhou Y, Zhang P, et al. Salvia miltiorrhiza Bunge: Bioactive Compounds and Bioactivities[J]. Int. J. Trad. Nat. Med, 2015, 5(1): 52-81.
[2] Hua Y, Yuan X, Shen Y, et al. Novel STAT3 inhibitors targeting STAT3 dimerization by binding to the STAT3 SH2 domain[J]. Frontiers in Pharmacology, 2022, 13: 836724.
[3] Li H, Gao C, Liu C, et al. A review of the biological activity and pharmacology of cryptotanshinone, an important active constituent in Danshen[J]. Biomedicine & Pharmacotherapy, 2021, 137: 111332.
[4] Hur J M, Shim J S, Jung H J, et al. Cryptotanshinone but not tanshinone IIA inhibits angiogenesis in vitro[J]. Experimental & molecular medicine, 2005, 37(2): 133-137.
[5] Chen L, Wang H J, Xie W, et al. Cryptotanshinone inhibits lung tumorigenesis and induces apoptosis in cancer cells in vitro and in vivo[J]. Molecular medicine reports, 2014, 9(6): 2447-2452.
[6] Jin H J, Li C G. Tanshinone IIA and cryptotanshinone prevent mitochondrial dysfunction in hypoxia‐induced H9c2 cells: association to mitochondrial ROS, intracellular nitric oxide, and calcium levels[J]. Evidence‐Based Complementary and Alternative Medicine, 2013, 2013(1): 610694.
[7] Li W, Yan H, Zhou Z, et al. Cryptotanshinone attenuated pathological cardiac remodeling in vivo and in vitro experiments[J]. Oxidative Medicine and Cellular Longevity, 2023, 2023(1): 4015199.
[8] Li Z, Zheng Y, Zhang L, et al. Cryptotanshinone alleviates liver fibrosis via inhibiting STAT3/CPT1A-dependent fatty acid oxidation in hepatic stellate cells[J]. Chemico-Biological Interactions, 2024, 399: 111119.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

A549 cells

Preparation Method

A549 cells were seeded in a 6-well plate at a density of 1x105/ml and treated at a final Cryptotanshinone concen tration of 20µM for 24h. Cells were trypsinized, centrifuged (4˚C, 800g/min, 10min), washed with PBS and fixed with cold 70% ethanol/30% PBS at 4˚C overnight. Cells were digested by RNase A, and then stained with 1% propidium iodide at 37˚C for 30min. The DNA profiles were determined within 4h of staining by flow cytometry. The expresions of cell cycle and apoptosis-associated genes was tested using Cell Cycle PCR Array.

Reaction Conditions

20μM; 24h

Applications

Following treatment with 20µM Cryptotanshinone, the percentage of A549 cells in G0/G1 phase was decreased while that in G2/M phases was increased. Cryptotanshinone was able to cause G2/M phase arrest in A549 cells.

Animal experiment [2]:

Animal models

Male C57BL/6J mice

Preparation Method

After Aortic Banding (AB) surgery, the mice were divided into four groups randomly: saline group (VEH), Cryptotanshinone (CTS) group, AB group, and AB+CTS group (n=10 in the sham group, n=10 in the AB group). Three days after AB surgery, mice were administrated with Cryptotanshinone for 4 weeks (50mg/kg, gastric perfusion). At the end of the treatment, the surviving mice were used for accessing cardiac function. And mice were euthanized with an overdose of sodium pentobarbital (200mg/kg, intraperitoneal injection). Hearts were collected for other experiments.

Dosage form

50mg/kg; 4 weeks; gastric perfusion

Applications

Cryptotanshinone treatment improved pressure overload-induced cardiac dysfunction, attenuated cardiac hypertrophy, and reduced cardiac fibrosis in mice.

References:
[1]Chen L, Wang H J, Xie W, et al. Cryptotanshinone inhibits lung tumorigenesis and induces apoptosis in cancer cells in vitro and in vivo[J]. Molecular medicine reports, 2014, 9(6): 2447-2452.
[2]Li W, Yan H, Zhou Z, et al. Cryptotanshinone attenuated pathological cardiac remodeling in vivo and in vitro experiments[J]. Oxidative Medicine and Cellular Longevity, 2023, 2023(1): 4015199.

وثائق المنتج (Product Documents)

Purity:>99.50%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
35825-57-1
الاسم الكيميائي
(1R)-1,6,6-trimethyl-2,7,8,9-tetrahydro-1H-naphtho[1,2-g][1]benzofuran-10,11-dione
SMILES
CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C
الصيغة الجزيئية
C19H20O3
الوزن الجزيئي
296.35
الذوبانية
≥ 4.23mg/mL in DMSO
التخزين
-20°C
إرشادات عامة
اختر مذيبًا مناسبًا وفقًا لبيانات ذوبانية المنتج. بعد التحضير، قسّم المحلول المخزون إلى أجزاء لتجنب دورات التجميد والذوبان المتكررة.
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
شروط الشحن
تُشحن عينات التقييم مع عبوات تبريد. وتُشحن الأحجام الأخرى المتاحة في درجة حرارة الغرفة، أو مع عبوات تبريد عند الطلب.

الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية

g/mol

Reviews

Review for Cryptotanshinone

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