GLPBio

SB 366791

Catalog No.: GC14997Purity:>98.00%
SB 366791 هو أحد مضادات مستقبلات الفانيليا القوية والانتقائية (VR1 / TRPV1) (IC50 \u003d 5.7 نانومتر).

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


SB 366791
Cas No.: 472981-92-3
10mM (in 1mL DMSO)In Stock
$44.00
1
1mgIn Stock
$20.00
1
5mgIn Stock
$40.00
1
10mgIn Stock
$56.00
1
25mgIn Stock
$120.00
1
50mgIn Stock
$192.00
1
100mgIn Stock
$288.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    Nature
    641, 529–536 (2025)
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    628, 630–638 (2024)
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    Nature
    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    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)
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    387(6739) (2025)
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    Science
    387(6734) (2025)
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    Cell Research
    35, 97–116 (2025)
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    34, 683–706 (2024)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

الوصف (Description)

SB 366791 is a potent and selective vanilloid receptor (VR1/TRPV1) antagonist with an IC50 value of 5.7nM [1]. SB 366791 can reduce the release rates of substance P (SP) and calcitonin gene-related peptide (CGRP) and alleviate thermal hyperalgesia [2]. SB 366791 has been widely used to limit morphine addiction in mice and alleviate the behavioral changes caused by opioids [3].

In vitro, SB 366791 (10µM) was pre-treated for 1 hour, which significantly inhibited HT22 cell apoptosis induced by sevoflurane, and reduced the increase in TRPV1 mRNA and protein expression [4]. Treatment with 3µM SB 366791 for 24 hours significantly inhibited the chemotactic activity of mouse-derived microglial cells induced by capsaicin and prevented the decrease in mitochondrial membrane potential[5].

In vivo, SB 366791 treatment via a single intraperitoneal injection at a dose of 500µg/kg for 20 minutes significantly inhibited the hypothermia, wiping movements, and vascular dilation of the knee joint induced by capsaicin in rats[6]. Oral administration of a 10mg/kg/day dose of SB 366791 for 15 days alleviated the epileptic seizures induced by pentylenetetrazole (PTZ) in mice, improved spatial cognitive impairment, and increased GSH levels[7].

References:
[1] Gunthorpe M J, Rami H K, Jerman J C, et al. Identification and characterisation of SB-366791, a potent and selective vanilloid receptor (VR1/TRPV1) antagonist[J]. Neuropharmacology, 2004, 46(1): 133-149.
[2] Mazeto T K, Picada J N, Correa Á P, et al. Antinociceptive and genotoxic assessments of the antagonist TRPV1 receptor SB-366791 on morphine-induced tolerance in mice[J]. Naunyn-Schmiedeberg's Archives of Pharmacology, 2020, 393(3): 481-490.
[3] Ma S X, Kwon S H, Seo J Y, et al. Impairment of opiate‐mediated behaviors by the selective TRPV1 antagonist SB366791[J]. Addiction biology, 2017, 22(6): 1817-1828.
[4] Liu Y, Yang H, Sun C, et al. Protective effects of TRPV1 inhibition against sevoflurane-induced cell death[J]. Neuroscience Letters, 2019, 707: 134270.
[5] Miyake T, Shirakawa H, Nakagawa T, et al. Activation of mitochondrial transient receptor potential vanilloid 1 channel contributes to microglial migration[J]. Glia, 2015, 63(10): 1870-1882.
[6] Varga A, Németh J, Szabó Á, et al. Effects of the novel TRPV1 receptor antagonist SB366791 in vitro and in vivo in the rat[J]. Neuroscience letters, 2005, 385(2): 137-142.
[7] Tian X, Xu X. Therapeutic Investigation of Zingerone Against Pentylenetetrazole-Induced Kindled Seizures in Mice[J]. Iranian Journal of Pharmaceutical Research: IJPR, 2025, 24(1): e162878.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

HT22 cells

Preparation Method

HT22 cells were cultured in DMEM medium supplemented with 100U/ml penicillin and 100mg/ml streptomycin in 5% CO2 at 37°C. Cells were placed in a 6 well-plate at a concentration of 1×106 cells per well for 24h. The cells were pretreated with 10μM SB 366791 for 1h. Then, cells were treated with 4% sevoflurane for 6h under 5% CO2 and 21% O2. The anesthetic sevoflurane was delivered from an anesthesia machine to a custom-made sealed acrylic glass chamber containing the cells in the incubator at 37℃. Cell apoptosis was conducted.

Reaction Conditions

10µM; 1h

Applications

SB 366791 treatment significantly reduced the sevoflurane-induced cell apoptosis in HT22 cells.
Animal experiment [2]:

Animal models

Male Swiss albino mice

Preparation Method

Male Swiss albino mice (12 months old; 20-30g) were housed in a specialized animal care facility, in a room with constant temperature (25°C), humidity control, and a 12/12h light/dark cycle with free access to food and water. Mice were subjected to recurrent intraperitoneal (i.p.) treatment with a 35mg/kg dose of PTZ to induce kindled seizures (KS) over three alternate days, i.e., day 1, 3, and 5. The KS-induced mice received oral SB 366791 (10mg/kg/day) for 15 days after the third dose of PTZ (from day 6). Assessment of Kindled Seizures-Induced Spatial Cognition by the Water Y-Maze Test.

Dosage form

10mg/kg/day for 15 days; p.o.

Applications

SB 366791 treatment significantly improved spatial cognitive impairment in KS-induced mice.

References:
[1] Liu Y, Yang H, Sun C, et al. Protective effects of TRPV1 inhibition against sevoflurane-induced cell death[J]. Neuroscience Letters, 2019, 707: 134270.
[2] Tian X, Xu X. Therapeutic Investigation of Zingerone Against Pentylenetetrazole-Induced Kindled Seizures in Mice[J]. Iranian Journal of Pharmaceutical Research: IJPR, 2025, 24(1): e162878.

وثائق المنتج (Product Documents)

Purity:>98.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
472981-92-3
الاسم الكيميائي
(E)-3-(4-chlorophenyl)-N-(3-methoxyphenyl)acrylamide
SMILES
ClC1=CC=C(C=C1)/C=C/C(NC2=CC=CC(OC)=C2)=O
الصيغة الجزيئية
C16H14ClNO2
الوزن الجزيئي
287.75
الذوبانية
≥ 12.35mg/mL in DMSO
التخزين
Store at RT
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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