GLPBio

Peimisine

Catalog No.: GN10319Purity:>98.00%
Peimisine is a kind of bioactive alkaloids found in Fritillaria bulbs which can inhibit angiotensin converting enzyme (ACE) activity with an IC50 of 526.5μM.

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


Peimisine
Cas No.: 19773-24-1
10mM (in 1mL DMSO)In Stock
$67.00
1
1mgIn Stock
$29.00
1
5mgIn Stock
$71.00
1
10mgIn Stock
$103.00
1
25mgIn Stock
$177.00
1
50mgIn Stock
$248.00
1
100mgIn Stock
$347.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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الوصف (Description)

Peimisine is a kind of bioactive alkaloids found in Fritillaria bulbs which can inhibit angiotensin converting enzyme (ACE) activity with an IC50 of 526.5μM [1]. Peimisine has anti-acute lung injury effect and has obvious cytotoxicity against various tumor cells [2, 3].

Peimisine (10, 20 and 40μM; 24h) reduced the reactive oxygen species (ROS), malondialdehyde (MDA) and 4-hydroxynonenal (4-HNE) content and restored the level of superoxide dismutase (SOD) in cigarette smoke extract (CSE)-induced BEAS-2B cells; Peimisine (10, 20 and 40μM; 24h) significantly decreased the number of apoptotic cells and the cell apoptosis rate in CSE-induced BEAS-2B cells [4]. Peimisine (160μM; 24h) significantly upregulated the expression of ADRB2 and NOS3 and downregulated the expression of SRC and MMP2 in BEAS-2B cells stimulated with CSE [5].

Peimisine (5 and 15mg/kg; 7d; p.o.) significantly alleviated the disease signs of colitis C57BL/C mice; Peimisine (5 and 15mg/kg; 7d; p.o.) significantly downregulated the expression levels of CD68 and CD11b in colitis C57BL/C mice [6].

References:
[1] Oh H, Kang D G, Lee S, et al. Angiotensin converting enzyme (ACE) inhibitory alkaloids from Fritillaria ussuriensis [J]. Planta medica, 2003, 69(6): 564-565.
[2] Jin X, Gao X, Lan M, et al. Study the mechanism of peimisine derivatives on NF-κB inflammation pathway on mice with acute lung injury induced by lipopolysaccharide [J]. Chemical biology & drug design, 2022, 99(5): 717-726.
[3] Wang D, Jiang Y, Wu K, et al. Evaluation of antitumor property of extracts and steroidal alkaloids from the cultivated Bulbus Fritillariae ussuriensis and preliminary investigation of its mechanism of action [J]. BMC complementary and alternative medicine, 2015, 15: 29.
[4] Liu C, Zhu X, Aga E, et al. Ebeiedinone and peimisine inhibit cigarette smoke extract-induced oxidative stress injury and apoptosis in BEAS-2B cells [J]. Cell stress & chaperones, 2024, 29(6): 697-708.
[5] Xian M, Xu J, Zheng Y, et al. Network pharmacology and experimental verification reveal the regulatory mechanism of Chuanbeimu in treating chronic obstructive pulmonary disease [J]. International journal of chronic obstructive pulmonary disease, 2024, 19: 799-813.
[6] Li Y, Yang X, Han J, et al. Peimisine ameliorates DSS-induced colitis by suppressing Jak-Stat activation and alleviating gut microbiota dysbiosis in mice [J]. The Journal of pharmacy and pharmacology, 2024, 76(5): 545-558.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

BEAS-2B cells

Preparation Method

BEAS-2B cells were stimulated with cigarette smoke extract (CSE) to induce oxidative stress injury. Cells were co-incubated with 0.5% CSE and peimisine (10, 20, and 40μM) for 24h and then the reactive oxygen species (ROS), malondialdehyde (MDA), superoxide dismutase (SOD) levels were measured using the kits and the level of 4-hydroxynonenal (4-HNE) was determined by enzyme-linked immunosorbent assay.

Reaction Conditions

10, 20 and 40μM; 24h

Applications

Peimisine reduced the ROS, MDA and 4-HNE content and restored the level of SOD.
Animal experiment [2]:

Animal models

Male C57BL/C mice

Preparation Method

Mice were received Peimisine (5 and 15mg/kg) via oral administration for 1 week before Dextran Sulfate Sodium (DSS) stimulation. All groups were subsequently treated with 2.5% DSS for 7 days to induce colitis. The disease activity index (DAI) was determined from days 0 to 7. DAI is the sum of scores for stool consistency, weight loss, and gross bleeding extent.

Dosage form

5 and 15mg/kg; 7d; p.o.

Applications

Peimisine significantly alleviated the disease signs of colitis induced by DSS.

References:
[1] Liu C, Zhu X, Aga E, et al. Ebeiedinone and peimisine inhibit cigarette smoke extract-induced oxidative stress injury and apoptosis in BEAS-2B cells [J]. Cell stress & chaperones, 2024, 29(6): 697-708.
[2] Li Y, Yang X, Han J, et al. Peimisine ameliorates DSS-induced colitis by suppressing Jak-Stat activation and alleviating gut microbiota dysbiosis in mice [J]. The Journal of pharmacy and pharmacology, 2024, 76(5): 545-558.

وثائق المنتج (Product Documents)

Purity:>98.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
19773-24-1
الاسم الكيميائي
3,9-bis(azepan-1-yl)-2,4,8,10-tetraoxa-3ж╦5,9ж╦5-diphosphaspiro[5.5]undecane 3,9-dioxide
SMILES
C1CCCN(CC1)P2(=O)OCC3(CO2)COP(=O)(OC3)N4CCCCCC4
الصيغة الجزيئية
C27H41NO3
الوزن الجزيئي
427.31
الذوبانية
≥ 50mg/mL in DMSO with ultrasonic and warming
التخزين
Store at 2-8°C, protect from light
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

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