>>Natural Products>>12-Deoxywithastramonolide

12-Deoxywithastramonolide (Synonyms: Baimantuoluoside C aglycone, 27-Hydroxywithanolide B)

Catalog No.GC18531 Copy One-Click Copy Product Info

12-Deoxywithastramonolide는 ashwagandha(W.

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12-Deoxywithastramonolide Chemical Structure

Cas No.: 60124-17-6

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1mg
US$81.00
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5mg
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10mg
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Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.



Description of 12-Deoxywithastramonolide

12-Deoxywithastramonolide is a natural lactone found in ashwagandha (W.somnifera)[1].

In vitro, 12-Deoxywithastramonolide (0-200µM; 24 or 48h) exhibited low cytotoxicity in J774A.1 macrophages[2]. 12-Deoxywithastramonolide (10µM; 24h) significantly inhibited NO production in LPS-activated J774A.1 macrophages[2]. 12-Deoxywithastramonolide (1.25-10µM; 24h) dose-dependently increased erythrocyte membrane stability and inhibited protein denaturation, with an IC₅₀ of 8.16µM[2].

In vivo, a single oral dose of 12-Deoxywithastramonolide (20mg/kg) significantly attenuated acute thermal nociception in mice, as evidenced by prolonged withdrawal latency to thermal stimulus[2]. A single oral dose of 12-Deoxywithastramonolide (20mg/kg) reduced acetic acid-induced abdominal constrictions in mice (writhing response), exhibiting a 32% inhibition[2]. A single oral dose of 12-Deoxywithastramonolide (20mg/kg) inhibited rat paw edema with a rate of approximately 38%[2].

References:
[1] Nile SH, Nile A, Gansukh E, Baskar V, Kai G. Subcritical water extraction of withanosides and withanolides from ashwagandha (Withania somnifera L) and their biological activities. Food Chem Toxicol. 2019;132:110659.
[2] Chandan G, Kumar C, Chibber P, et al. Evaluation of analgesic and anti-inflammatory activities and molecular docking analysis of steroidal lactones from Datura stramonium L. Phytomedicine. 2021;89:153621.

Protocol of 12-Deoxywithastramonolide

Cell experiment [1]:

Cell lines

J774A.1 mouse BALB/c macrophages

Preparation Method

Following 24h incubation, macrophages were incubated for 2h with 100ng/mL LPS, preceded by 12-Deoxywithastramonolide (10µM) treatment at 37°C in 5% CO2. Diclofenac (10µM) was used as positive control. After 2, 12 and 24h of lactone treatment, supernatant was collected and kept at -80°C for the quantification of nitric oxide (NO) using the Griess reaction with slight modifications.

Reaction Conditions

10µM; 24h

Applications

12-Deoxywithastramonolide significantly inhibited NO production in LPS-activated macrophages.
Animal experiment [1]:

Animal models

Mice

Preparation Method

Tail-flick assay: The mouse tail (3-5cm) was kept on the analgesiometer nichrome wire after that the reaction time was measured in terms of tail removal. A reaction time was recorded as the interval between tail exposure to the hot beam and the tail withdrawal reflex. Reaction times to analyze pain were recorded at 0-4h at different intervals after the oral administration of 12-Deoxywithastramonolide (20mg/kg). A cut-off time of 20s was enacted as a protection against skin damage. Diclofenac at a dose of 50 mg/kg was used as a reference drug.

Dosage form

20mg/kg; p.o.; once

Applications

12-Deoxywithastramonolide significantly decreased the acute thermal nociception in mice (0.5-2h) and extended the animal’s response time to the temperature incitement when compared to the vehicle-treated control.

References:
[1] Chandan G, Kumar C, Chibber P, et al. Evaluation of analgesic and anti-inflammatory activities and molecular docking analysis of steroidal lactones from Datura stramonium L. Phytomedicine. 2021;89:153621.

Chemical Properties of 12-Deoxywithastramonolide

Cas No. 60124-17-6 SDF
Synonyms Baimantuoluoside C aglycone, 27-Hydroxywithanolide B
Chemical Name 6α,7α-epoxy-5α,22R,27-trihydroxy-1-oxo-ergosta-2,24-dien-26-oic acid δ-lactone
Canonical SMILES CC(C1)=C(CO)C(O[C@@]1([H])[C@@H](C)[C@@]2([H])CC[C@@]3([H])[C@]4([H])[C@H]5[C@H](O5)[C@@]([C@@]6(C)[C@@]4([H])CC[C@@]32C)(O)CC=CC6=O)=O
Formula C28H38O6 M.Wt 470.6
Solubility DMF: 2 mg/ml,DMSO: 0.1 mg/ml,Ethanol: 20 mg/ml,Ethanol:PBS (pH 7.2)(1:2): 0.3 mg/ml Storage Store at -20°C,protect from light
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of 12-Deoxywithastramonolide

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 2.1249 mL 10.6247 mL 21.2495 mL
5 mM 425 μL 2.1249 mL 4.2499 mL
10 mM 212.5 μL 1.0625 mL 2.1249 mL
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In vivo Formulation Calculator (Clear solution) of 12-Deoxywithastramonolide

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL saline, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
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Average Rating: 5 ★★★★★ (Based on Reviews and 31 reference(s) in Google Scholar.)

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