Neocryptotanshinone (Synonyms: 新隐丹参酮)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Neocryptotanshinone  (Synonyms: 新隐丹参酮) 纯度: 98.82%

Neocryptotanshinone 是从丹参 (Salvia Miltiorrhiza) 分离得到的一种丹参二萜,通过抑制 NF-κBiNOS 信号来抑制脂多糖 (LPS) 诱导的炎症。

Neocryptotanshinone                                          (Synonyms: 新隐丹参酮)

Neocryptotanshinone Chemical Structure

CAS No. : 109664-02-0

规格 价格 是否有货 数量
1 mg ¥1400 In-stock
5 mg ¥2800 In-stock
10 mg ¥5000 In-stock
50 mg   询价  
100 mg   询价  

* Please select Quantity before adding items.

Neocryptotanshinone 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Immunology/Inflammation Compound Library
  • NF-κB Signaling Compound Library
  • Stem Cell Signaling Compound Library
  • Natural Product Library
  • Anti-Aging Compound Library
  • Antioxidant Compound Library
  • Differentiation Inducing Compound Library
  • Oxygen Sensing Compound Library
  • Terpenoids Library
  • Pyroptosis Compound Library
  • Traditional Chinese Medicine Active Compound Library
  • Neuroprotective Compound Library
  • Anti-Breast Cancer Compound Library
  • Anti-Pancreatic Cancer Compound Library
  • Anti-Blood Cancer Compound Library
  • Anti-Cancer Metabolism Compound Library
  • Anti-Obesity Compound Library
  • Angiogenesis-Related Compound Library
  • Transcription Factor-Targeted Library
  • Anti-Liver Cancer Compound Library
  • Antidepressant Compound Library
  • Anti-inflammatory Traditional Chinese Medicine Active Compound Library
  • Plant-Sourced Natural Product Library
  • Anti-Prostate Cancer Compound Library
  • Anti-Pulmonary Fibrosis Compound Library
  • Cancer Stem Cells Compound Library
  • Pain-Related Compound Library
  • Mitochondrial Protection Compound Library
  • Metabolic Enzyme Compound Library
  • Membrane Protein-targeted Compound Library
  • Anti-Hematopathy Compound Library
  • Anti-Ovarian Cancer Compound Library
  • Multi-Target Compound Library
  • Radioprotector Library

同靶点产品:

同靶点蛋白产品:

生物活性

Neocryptotanshinone, a fatty diterpenoids from Salvia Miltiorrhiza, inhibits lipopolysaccharide-induced inflammation by suppression of NF-κB and iNOS signaling pathways[1][2].

IC50 & Target

iNOS

 

体外研究
(In Vitro)

Neocryptotanshinone exhibits anti-inflammatory effect by suppression of NF-κB and iNOS signaling pathways[1].
Neocryptotanshinone (10 μM and 20 μM, 24 h) inhibits LPS-induced iNOS protein expression in RAW264.7 cells[1].
Neocryptotanshinone (20 μM, 24 h) shows no obvious cytotoxic effect towards murine RAW264.7 macrophages[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Neocryptotanshinone 相关抗体:

Cell Viability Assay[1]

Cell Line: RAW264.7 cells
Concentration: 5, 10 and 20 μM
Incubation Time: 24 hours
Result: Inhibited LPS-induced cell viability in a dose-dependent manner.

Western Blot Analysis[1]

Cell Line: RAW264.7 cells
Concentration: 20 μM
Incubation Time: 24 hours
Result: Inhibited LPS-induced activation of NF-κB pathway and down-regulated LPS-induced expression of p-NF-κB p65, p-IκBα and p-IKKβ.

体内研究
(In Vivo)

Neocryptotanshinone causes reversals of decreased pain thresholds induced by MSU treatment after 30, 60, and 120 min S. miltiorrhiza Bunge extract treatment (contains single active components)[3].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: MSU-induced pain model in male ICR mice (weighing 20-25 g)[2]
Dosage: 10, 25, 50 or 100 mg/kg
Administration: Oral gavage; for 30, 60, 120 min
Result: Inhibited inflammatory symptoms and nociceptive behaviors in a dose-dependent manner.

分子量

314.38

Formula

C19H22O4

CAS 号

109664-02-0

性状

固体

颜色

Light yellow to yellow

中文名称

新隐丹参酮

结构分类
  • Terpenoids
  • Diterpenoids
  • Quinones
  • Naphthalene Quinones
初始来源
  • 植物
  • 豆科
  • 雨树
  • 植物
  • 唇形科
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性数据
In Vitro: 

DMSO 中的溶解度 : 100 mg/mL (318.09 mM; 超声助溶; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 3.1809 mL 15.9043 mL 31.8086 mL
5 mM 0.6362 mL 3.1809 mL 6.3617 mL
10 mM 0.3181 mL 1.5904 mL 3.1809 mL

查看完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (protect from light)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量

=

浓度

×

体积

×

分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×

体积 (start)

V1

=

浓度 (final)

C2

×

体积 (final)

V2

扫码获得
动物溶解方案

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量

计算结果
工作液所需浓度 : mg/mL

纯度 & 产品资料

纯度: 98.82%

Data Sheet (603 KB) SDS (251 KB)

COA (264 KB) HNMR (154 KB) RP-HPLC (244 KB) MS (78 KB)

产品使用指南 (1538 KB)

参考文献
  • [1]. Chuanhong Wu, et al. Neocryptotanshinone Inhibits Lipopolysaccharide-Induced Inflammation in RAW264.7 Macrophages by Suppression of NF-κB and iNOS Signaling Pathways. Acta Pharm Sin B. 2015 Jul;5(4):323-9.  [Content Brief]

    [2]. H C Lin, et al. Two New Fatty Diterpenoids From Salvia Miltiorrhiza. J Nat Prod. 2001 May;64(5):648-50.  [Content Brief]

    [3]. FENG Jinghui, et al. Effects of Salvia miltiorrhiza Bunge extract and its single components on monosodium urate-induced pain in vivo and lipopolysaccharide-induced inflammation in vitro. J Tradit Chin Med. 2021. 41(2): 219-226.  [Content Brief]

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务