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12-Deoxywithastramonolide

Catalog No.: GC18531Purity:>95.50%Synonyms: Baimantuoluoside C aglycone, 27-Hydroxywithanolide B
12-Deoxywithastramonolide는 ashwagandha(W.

제품은 연구용으로만 사용됩니다. 인체에 사용할 수 없으며 환자에게 판매하지 않습니다.


12-Deoxywithastramonolide
Cas No.: 60124-17-6
1mgIn Stock
$81.00
1
5mgIn Stock
$243.00
1
10mgIn Stock
$351.00
1

인용 문헌 (Citations)

현재 이 제품에 대한 인용 문헌이 없습니다. 아래는 GlpBio 제품을 인용한 주요 논문입니다.
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    641, 529–536 (2025)
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    632, 686–694 (2024)
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    183(7):1867-1883 (2020)
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제품 설명 (Description)

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.

실험 프로토콜 (Protocol)

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.

제품 문서 (Product Documents)

Purity:>95.50%Appearance:A solid

화학적 특성 (Chemical Properties)

CAS 번호
60124-17-6
동의어
Baimantuoluoside C aglycone, 27-Hydroxywithanolide B
화학명
6α,7α-epoxy-5α,22R,27-trihydroxy-1-oxo-ergosta-2,24-dien-26-oic acid δ-lactone
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
분자식
C28H38O6
분자량
470.6
용해도
DMF: 2 mg/ml,DMSO: 0.1 mg/ml,Ethanol: 20 mg/ml,Ethanol:PBS (pH 7.2)(1:2): 0.3 mg/ml
보관
Store at -20°C,protect from light
일반 주의사항
제품의 용해도 데이터에 따라 적절한 용매를 선택하십시오. 조제 후에는 반복적인 동결·해동을 피할 수 있도록 저장 용액을 소분하십시오.
저장 용액은 -80°C 보관 시 6개월 이내, -20°C 보관 시 1개월 이내에 사용하십시오.
용해도를 높이려면 튜브를 37°C로 데운 뒤 적절한 시간 동안 초음파 처리하십시오.
배송 조건
평가용 샘플은 아이스팩과 함께 배송됩니다. 그 외 용량은 실온 배송되며, 요청 시 아이스팩과 함께 배송할 수 있습니다.

계산 도구 (Calculators)몰 농도 / 희석 / 분자량 / 단위 변환 / 생체 내 제형 / 용해도

g/mol

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