1. Apoptosis
  2. Apoptosis
  3. Liriodenine

Liriodenine  (Synonyms: Spermatheridine; VLT045)

目录号: HY-N3376
产品使用指南 技术支持

Liriodenine (Spermatheridine;VLT045) 是从植物 Mitrephora sirikitiae 中分离出来的,具有抗癌活性。Liriodenine 诱导细胞凋亡 (apoptosis),通过诱导 caspase-3 和 caspase-9 激活其内在通路。

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Liriodenine Chemical Structure

Liriodenine Chemical Structure

CAS No. : 475-75-2

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Liriodenine (Spermatheridine; VLT045) is an aporphine alkaloid isolated from the plant?Mitrephora sirikitiae?and has anti-cancer activities[1]. Liriodenine induces cell apoptosis, activates the intrinsic pathway by induction of caspase-3 and caspase-9[2].

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
B16-F10 IC50
> 10 μM
Compound: 20
Cytotoxicity against mouse B16-F10 cells assessed as reduction in cell viability incubated for 72 hrs by Alamar blue assay
Cytotoxicity against mouse B16-F10 cells assessed as reduction in cell viability incubated for 72 hrs by Alamar blue assay
[PMID: 27300257]
BV-2 IC50
5 μM
Compound: 13
Antineuroinflammatory activity against mouse BV2 cells assessed as inhibition of LPS-induced NO production incubated for 20 hrs by Griess assay
Antineuroinflammatory activity against mouse BV2 cells assessed as inhibition of LPS-induced NO production incubated for 20 hrs by Griess assay
[PMID: 33822610]
HepG2 IC50
8.3 μM
Compound: 20
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability incubated for 72 hrs by Alamar blue assay
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability incubated for 72 hrs by Alamar blue assay
[PMID: 27300257]
HL-60 IC50
5.5 μM
Compound: 20
Cytotoxicity against human HL-60 cells assessed as reduction in cell viability incubated for 72 hrs by Alamar blue assay
Cytotoxicity against human HL-60 cells assessed as reduction in cell viability incubated for 72 hrs by Alamar blue assay
[PMID: 27300257]
HT-29 IC50
> 10 μM
Compound: 6
Cytotoxicity against human HT-29 cells assessed as inhibition of cell proliferation after 3 days by SRB assay
Cytotoxicity against human HT-29 cells assessed as inhibition of cell proliferation after 3 days by SRB assay
[PMID: 23327794]
K562 IC50
5 μM
Compound: 20
Cytotoxicity against human K562 cells assessed as reduction in cell viability incubated for 72 hrs by Alamar blue assay
Cytotoxicity against human K562 cells assessed as reduction in cell viability incubated for 72 hrs by Alamar blue assay
[PMID: 27300257]
KB IC50
5 μM
Compound: 9
Cytotoxicity against human KB cells after 3 days by sulforhodamine B assay
Cytotoxicity against human KB cells after 3 days by sulforhodamine B assay
[PMID: 19874044]
MCF7 IC50
5 μM
Compound: 9
Cytotoxicity against human MCF7 cells after 3 days by sulforhodamine B assay
Cytotoxicity against human MCF7 cells after 3 days by sulforhodamine B assay
[PMID: 19874044]
NCI-H460 IC50
5 μM
Compound: 9
Cytotoxicity against human NCI-H460 cells after 3 days by sulforhodamine B assay
Cytotoxicity against human NCI-H460 cells after 3 days by sulforhodamine B assay
[PMID: 19874044]
PBMC IC50
34.8 μM
Compound: 20
Cytotoxicity against human PBMC cells assessed as reduction in cell viability incubated for 72 hrs by Alamar blue assay
Cytotoxicity against human PBMC cells assessed as reduction in cell viability incubated for 72 hrs by Alamar blue assay
[PMID: 27300257]
RAW264.7 IC50
1.39 μM
Compound: 129
Inhibition of NO production in LPS-stimulated mouse RAW264.7 cells incubated for 24 hrs by Griess reagent-based assay
Inhibition of NO production in LPS-stimulated mouse RAW264.7 cells incubated for 24 hrs by Griess reagent-based assay
[PMID: 33454546]
RAW264.7 IC50
10.5 μM
Compound: 10
Antiinflammatory activity in mouse RAW264.7 assessed as inhibition of LPS-induced NO production preincubated for 30 mins followed by LPS stimulation measured after 24 hrs by Griess reagent based assay
Antiinflammatory activity in mouse RAW264.7 assessed as inhibition of LPS-induced NO production preincubated for 30 mins followed by LPS stimulation measured after 24 hrs by Griess reagent based assay
[PMID: 33939429]
RAW264.7 IC50
34.7 μM
Compound: 6
Inhibition of LPS-stimulated nitric oxide production in mouse RAW264.7 cells incubated for 24 hrs by Griess reagent-based assay
Inhibition of LPS-stimulated nitric oxide production in mouse RAW264.7 cells incubated for 24 hrs by Griess reagent-based assay
[PMID: 32247751]
SF-268 IC50
5 μM
Compound: 9
Cytotoxicity against human SF268 cells after 3 days by sulforhodamine B assay
Cytotoxicity against human SF268 cells after 3 days by sulforhodamine B assay
[PMID: 19874044]
体外研究
(In Vitro)

Liriodenine is against P-388, KB, HT-29, MCF-7, A549, ASK and Hek-293 cells with IC50 values of 9.60 μM, 11.02 μM, 10.62 μM, 9.20 μM and 8.07μM, respectively.

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

275.26

Formula

C17H9NO3

CAS 号
结构分类
初始来源
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

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

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

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

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
Liriodenine
目录号:
HY-N3376
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