GLPBio

(±)-Blebbistatin

Catalog No.: GC12341Purity:>99.00%Synonyms: (S)Blebbistatin
(± ؛) - Blebbistatin هو مثبط انتقائي للميوسين II (NMII) غير عضلي ، يعزز الهجرة الاتجاهية للخلايا البطانية للقرنية (CECs) ويسرع التئام الجروح ، ويحافظ بشكل أفضل على سلامة توصيل الخلايا ووظيفة الحاجز.

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


(±)-Blebbistatin
Cas No.: 674289-55-5
10mM 1 mL in DMSOIn Stock
$79.00
1
5mgIn Stock
$72.00
1
10mgIn Stock
$135.00
1
25mgIn Stock
$225.00
1
50mgIn Stock
$405.00
1
100mgIn Stock
$689.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    641, 529–536 (2025)
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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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    31, 1291–1307 (2021)

الوصف (Description)

(±)-Blebbistatin is a racemic mixture containing two configurations, (+)-Blebbistatinb and (-)-Blebbistatin (Cat. No. GC13430). (±)-Blebbistatin can effectively inhibit the activity of non-muscle myosin II ATPase and the expression of various striated muscle myosins and non-muscle myosins in vertebrates[1, 2]. (±)-Blebbistatin is a commonly used excitation-contraction uncoupling agent in cardiovascular physiology[3]. (±)-Blebbistatin is a potential photodynamic drug that can kill cancer cells. Exposure to UV light with a wavelength below 488nm can also lead to rapid inhibition of (±)-Blebbistatin[4].

In vitro, (±)-Blebbistatin (0.1, 0.5, 2, 10μM) treated rat ventricular myocytes for 10min prevented cell shortening in a dose-dependent manner with an IC50 of 0.43μM, but did not affect intracellular calcium transients ([Ca2+]i)[5].

In vivo, (±)-Blebbistatin (125nM/kg) treated rats with detrusor overactivity (DO) by intravesical instillation significantly reduced the detrusor overactivity index, non-micturition contraction amplitude, and non-micturition contraction frequency, and improved urine storage without impairing urination function[6]. (±)-Blebbistatin (125nM/kg) treated DO rats by intra-arterial injection attenuated 13-cis-RA-induced changes in cystometric parameters and central and peripheral neurotrophic factor levels, and also had antidepressant-like effects[7].

References:
[1]Lucas‐Lopez C, Patterson S, Blum T, et al. Absolute Stereochemical Assignment and Fluorescence Tuning of the Small Molecule Tool,(–)‐Blebbistatin[J]. 2005.
[2]Limouze J, Straight A F, Mitchison T, et al. Specificity of blebbistatin, an inhibitor of myosin II[J]. Journal of Muscle Research & Cell Motility, 2004, 25: 337-341.
[3]George S A , Lin Z , Efimov I R .Simultaneous triple-parametric optical mapping of transmembrane potential, intracellular calcium and NADH for cardiac physiology assessment[J].Communications Biology, 2024.
[4]Sakamoto T, Limouze J, Combs C A, et al. Blebbistatin, a myosin II inhibitor, is photoinactivated by blue light[J]. Biochemistry, 2005, 44(2): 584-588.
[5]Fedorov V V, Lozinsky I T, Sosunov E A, et al. Application of blebbistatin as an excitation–contraction uncoupler for electrophysiologic study of rat and rabbit hearts[J]. Heart rhythm, 2007, 4(5): 619-626.
[6]Wróbel A, Nowakowski Ł, Doboszewska U, et al. Blebbistatin reveals beneficial effects on the cystometric parameters in an animal model of detrusor overactivity[J]. Naunyn-schmiedeberg's Archives of Pharmacology, 2019, 392: 843-850.
[7]Wróbel A, Doboszewska U, Rechberger E, et al. Blebbistatin, a myosin II inhibitor, exerts antidepressant-like activity and suppresses detrusor overactivity in an animal model of depression coexisting with overactive bladder[J]. Neurotoxicity Research, 2019, 35: 196-207.

البروتوكول (Protocol)

Cell experiment [1]:

Cell lines

Rat ventricular myocytes

Preparation Method

Fluo-5F–loaded myocytes were placed in an open chamber on an inverted stage microscope with epifluorescence objectives and perfused with physiologic salt-containing solution (PSS) at 0.5mL/min. Cells continuously received either PSS alone or PSS with 0.1, 0.5, 2, or 10µM (±)-Blebbistatin. Each cell was exposed to only one blebbistatin concentration. Contraction and calcium transients ([Ca2+]i) were evaluated at baseline and after 10min of blebbistatin application in steady-state conditions. Cell shortening was recorded using IonOptix Digital Sarcomere Length software (IonOptix).

Reaction Conditions

0.1, 0.5, 2, or 10µM; 10min

Applications

In single rat ventricular cells, (±)-Blebbistatin blocked cell shortening in a dose-dependent manner with an IC50 of 0.43µM. However, even at the highest concentration (10µM), it did not affect the [Ca2+]i.

Animal experiment [2]:

Animal models

Wistar rats

Preparation Method

Rats were randomly divided into groups that received intravesical instillation of Retinyl acetate (RA) or polysorbate 80 in saline. Three days after, each group was subdivided into groups that received (±)-Blebbistatin intravesically (125nM/kg) or DMSO, and immediately after cystometric assessment was performed.

Dosage form

125nM/kg; intravesical instillation

Applications

(±)-Blebbistatin improves urine storage with no impairment of the voiding function. The significant reduction of the detrusor overactivity index, amplitude of nonvoiding contractions, and frequency of nonvoiding contractions in animals with detrusor overactivity (DO), following (±)-Blebbistatin administration.

References:
[1] Fedorov V V, Lozinsky I T, Sosunov E A, et al. Application of blebbistatin as an excitation–contraction uncoupler for electrophysiologic study of rat and rabbit hearts[J]. Heart rhythm, 2007, 4(5): 619-626.
[2]Wróbel A, Nowakowski Ł, Doboszewska U, et al. Blebbistatin reveals beneficial effects on the cystometric parameters in an animal model of detrusor overactivity[J]. Naunyn-schmiedeberg's Archives of Pharmacology, 2019, 392: 843-850.

وثائق المنتج (Product Documents)

Purity:>99.00%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
674289-55-5
المرادفات
(S)Blebbistatin
الاسم الكيميائي
3a-hydroxy-6-methyl-1-phenyl-3,3a-dihydro-1H-pyrrolo[2,3-b]quinolin-4(2H)-one
SMILES
OC12CCN(C1=NC3=C(C2=O)C=C(C=C3)C)C4=CC=CC=C4
الصيغة الجزيئية
C18H16N2O2
الوزن الجزيئي
292.34
الذوبانية
10mg/mL in DMSO, 20mg/mL in DMF
التخزين
Store at -20°C,unstable in solution, ready to use.
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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