1. 天然物
  2. Plants Flavonoids
  3. Selaginellaceae Biflavones
  4. Selaginella lepidophylla (Hook. & Grev.) Spring
  5. Robustaflavone

Robustaflavone is a biflavonoid isolated from Doradilla that has natriuretic properties.

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Robustaflavone

Robustaflavone 構造式

CAS 番号 : 49620-13-5

容量 価格(税別) 在庫状況 数量
1 mg $440 在庫あり
5 mg $1012 お問い合わせ
10 mg   お問い合わせ  
50 mg   お問い合わせ  

* アイテムを追加する前、数量をご選択ください

This product is a controlled substance and not for sale in your territory.

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  • 生物活性

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製品説明

Robustaflavone is a biflavonoid isolated from Doradilla that has natriuretic properties[1].

Cellular Effect
Cell Line Type Value Description References
A549 IC50
21.38 3
Compound: 7
Cytotoxicity against human A549 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
A549 IC50
21.38 3
Compound: 7
Cytotoxicity against human A549 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
A549 IC50
21.38 3
Compound: 7
Cytotoxicity against human A549 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human A549 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
Calu-1 IC50
> 100 3
Compound: 5
Cytotoxicity against human Calu1 cells after 3 days
Cytotoxicity against human Calu1 cells after 3 days
[PMID: 10843573]
Calu-1 IC50
>100 3
Compound: 5
Cytotoxicity against human Calu1 cells after 3 days
Cytotoxicity against human Calu1 cells after 3 days
[PMID: 10843573]
Calu-1 IC50
> 100 3
Compound: 5
Cytotoxicity against human Calu1 cells after 3 days
Cytotoxicity against human Calu1 cells after 3 days
[PMID: 10843573]
HeLa IC50
>100 3
Compound: 5
Cytotoxicity against human HeLa cells after 3 days
Cytotoxicity against human HeLa cells after 3 days
[PMID: 10843573]
HeLa IC50
> 100 3
Compound: 5
Cytotoxicity against human HeLa cells after 3 days
Cytotoxicity against human HeLa cells after 3 days
[PMID: 10843573]
HeLa IC50
> 100 3
Compound: 5
Cytotoxicity against human HeLa cells after 3 days
Cytotoxicity against human HeLa cells after 3 days
[PMID: 10843573]
HepG2 EC50
0.25 3
Compound: Robustaflavone (RF)
Effective concentration necessary to decrease extracellular Hepatitis B virus DNA levels by 50% in human hepatoblastoma cell line (2.2.15 cells) in vitro
Effective concentration necessary to decrease extracellular Hepatitis B virus DNA levels by 50% in human hepatoblastoma cell line (2.2.15 cells) in vitro
10.1016/S0960-894X(97)00422-8
HepG2 EC50
0.25 3
Compound: Robustaflavone (RF)
Effective concentration necessary to decrease extracellular Hepatitis B virus DNA levels by 50% in human hepatoblastoma cell line (2.2.15 cells) in vitro
Effective concentration necessary to decrease extracellular Hepatitis B virus DNA levels by 50% in human hepatoblastoma cell line (2.2.15 cells) in vitro
10.1016/S0960-894X(97)00422-8
HepG2 EC50
0.25 3
Compound: Robustaflavone (RF)
Effective concentration necessary to decrease extracellular Hepatitis B virus DNA levels by 50% in human hepatoblastoma cell line (2.2.15 cells) in vitro
Effective concentration necessary to decrease extracellular Hepatitis B virus DNA levels by 50% in human hepatoblastoma cell line (2.2.15 cells) in vitro
10.1016/S0960-894X(97)00422-8
HepG2 IC50
19.15 3
Compound: 7
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
HepG2 IC50
19.15 3
Compound: 7
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
HepG2 IC50
337 3
Compound: Robustaflavone (RF)
Cytotoxicity towards human hepatoblastoma cell line (2.2.15 cells) measured by inhibition of neutral red dye uptake in vitro
Cytotoxicity towards human hepatoblastoma cell line (2.2.15 cells) measured by inhibition of neutral red dye uptake in vitro
10.1016/S0960-894X(97)00422-8
HepG2 IC50
337 3
Compound: Robustaflavone (RF)
Cytotoxicity towards human hepatoblastoma cell line (2.2.15 cells) measured by inhibition of neutral red dye uptake in vitro
Cytotoxicity towards human hepatoblastoma cell line (2.2.15 cells) measured by inhibition of neutral red dye uptake in vitro
10.1016/S0960-894X(97)00422-8
HepG2 IC50
19.15 3
Compound: 7
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human HepG2 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
K562 IC50
>100 3
Compound: 5
Cytotoxicity against human K562 cells after 3 days
Cytotoxicity against human K562 cells after 3 days
[PMID: 10843573]
K562 IC50
> 100 3
Compound: 5
Cytotoxicity against human K562 cells after 3 days
Cytotoxicity against human K562 cells after 3 days
[PMID: 10843573]
HepG2 IC50
337 3
Compound: Robustaflavone (RF)
Cytotoxicity towards human hepatoblastoma cell line (2.2.15 cells) measured by inhibition of neutral red dye uptake in vitro
Cytotoxicity towards human hepatoblastoma cell line (2.2.15 cells) measured by inhibition of neutral red dye uptake in vitro
10.1016/S0960-894X(97)00422-8
MGC-803 IC50
15.57 3
Compound: 7
Cytotoxicity against human MGC803 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human MGC803 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
MGC-803 IC50
15.57 3
Compound: 7
Cytotoxicity against human MGC803 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human MGC803 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
K562 IC50
> 100 3
Compound: 5
Cytotoxicity against human K562 cells after 3 days
Cytotoxicity against human K562 cells after 3 days
[PMID: 10843573]
Neutrophil IC50
0.45 3
Compound: 6
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release pretreated for 5 mins followed by fMLP/CB stimulation using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as substrate
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release pretreated for 5 mins followed by fMLP/CB stimulation using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as substrate
[PMID: 29381070]
Neutrophil IC50
0.45 3
Compound: 6
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release pretreated for 5 mins followed by fMLP/CB stimulation using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as substrate
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release pretreated for 5 mins followed by fMLP/CB stimulation using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as substrate
[PMID: 29381070]
MGC-803 IC50
15.57 3
Compound: 7
Cytotoxicity against human MGC803 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human MGC803 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
Neutrophil IC50
1.01 3
Compound: 6
Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation pretreated for 5 mins followed by cytochalasin B addition for 3 mins and subsequent fMLP stimulation for 10 mins by superoxide dismutase
Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation pretreated for 5 mins followed by cytochalasin B addition for 3 mins and subsequent fMLP stimulation for 10 mins by superoxide dismutase
[PMID: 29381070]
Neutrophil IC50
0.45 3
Compound: 6
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release pretreated for 5 mins followed by fMLP/CB stimulation using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as substrate
Antiinflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release pretreated for 5 mins followed by fMLP/CB stimulation using MeO-Suc-Ala-Ala-Pro-Val-p-nitroanilide as substrate
[PMID: 29381070]
Neutrophil IC50
1.01 3
Compound: 6
Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation pretreated for 5 mins followed by cytochalasin B addition for 3 mins and subsequent fMLP stimulation for 10 mins by superoxide dismutase
Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation pretreated for 5 mins followed by cytochalasin B addition for 3 mins and subsequent fMLP stimulation for 10 mins by superoxide dismutase
[PMID: 29381070]
PBMC IC50
77 3
Compound: 3
Cytotoxicity against uninfected PHA-stimulated human PBMC assessed as thymidine incorporation after 24 hrs by trypan blue exclusion method
Cytotoxicity against uninfected PHA-stimulated human PBMC assessed as thymidine incorporation after 24 hrs by trypan blue exclusion method
[PMID: 9322359]
PBMC IC50
77 3
Compound: 3
Cytotoxicity against uninfected PHA-stimulated human PBMC assessed as thymidine incorporation after 24 hrs by trypan blue exclusion method
Cytotoxicity against uninfected PHA-stimulated human PBMC assessed as thymidine incorporation after 24 hrs by trypan blue exclusion method
[PMID: 9322359]
Neutrophil IC50
1.01 3
Compound: 6
Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation pretreated for 5 mins followed by cytochalasin B addition for 3 mins and subsequent fMLP stimulation for 10 mins by superoxide dismutase
Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation pretreated for 5 mins followed by cytochalasin B addition for 3 mins and subsequent fMLP stimulation for 10 mins by superoxide dismutase
[PMID: 29381070]
Raji IC50
> 100 3
Compound: 5
Cytotoxicity against human Raji cells after 3 days
Cytotoxicity against human Raji cells after 3 days
[PMID: 10843573]
Raji IC50
>100 3
Compound: 5
Cytotoxicity against human Raji cells after 3 days
Cytotoxicity against human Raji cells after 3 days
[PMID: 10843573]
T-24 IC50
21.09 3
Compound: 7
Cytotoxicity against human T24 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human T24 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
T-24 IC50
21.09 3
Compound: 7
Cytotoxicity against human T24 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human T24 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
Vero IC50
>100 3
Compound: 5
Cytotoxicity against african green monkey Vero cells after 3 days
Cytotoxicity against african green monkey Vero cells after 3 days
[PMID: 10843573]
Vero IC50
> 100 3
Compound: 5
Cytotoxicity against african green monkey Vero cells after 3 days
Cytotoxicity against african green monkey Vero cells after 3 days
[PMID: 10843573]
PBMC IC50
77 3
Compound: 3
Cytotoxicity against uninfected PHA-stimulated human PBMC assessed as thymidine incorporation after 24 hrs by trypan blue exclusion method
Cytotoxicity against uninfected PHA-stimulated human PBMC assessed as thymidine incorporation after 24 hrs by trypan blue exclusion method
[PMID: 9322359]
WISH IC50
> 100 3
Compound: 5
Cytotoxicity against human Wish cells after 3 days
Cytotoxicity against human Wish cells after 3 days
[PMID: 10843573]
WISH IC50
>100 3
Compound: 5
Cytotoxicity against human Wish cells after 3 days
Cytotoxicity against human Wish cells after 3 days
[PMID: 10843573]
Raji IC50
> 100 3
Compound: 5
Cytotoxicity against human Raji cells after 3 days
Cytotoxicity against human Raji cells after 3 days
[PMID: 10843573]
T-24 IC50
21.09 3
Compound: 7
Cytotoxicity against human T24 cells assessed as reduction in cell viability after 48 hrs by MTT assay
Cytotoxicity against human T24 cells assessed as reduction in cell viability after 48 hrs by MTT assay
[PMID: 29921475]
Vero IC50
> 100 3
Compound: 5
Cytotoxicity against african green monkey Vero cells after 3 days
Cytotoxicity against african green monkey Vero cells after 3 days
[PMID: 10843573]
WISH IC50
> 100 3
Compound: 5
Cytotoxicity against human Wish cells after 3 days
Cytotoxicity against human Wish cells after 3 days
[PMID: 10843573]
分子量

538.46

分子式

C30H18O10

CAS 番号
Appearance

Solid

Color

Light yellow to yellow

SMILES

O=C1C=C(C2=CC=C(O)C=C2)OC3=CC(O)=C(C4=CC(C5=CC(C6=C(O)C=C(O)C=C6O5)=O)=CC=C4O)C(O)=C13

Structure Classification
Initial Source
輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶剤 & 溶解度
体外: 

DMSO : 10 mg/mL (18.57 mM; Need ultrasonic and warming; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.8571 mL 9.2857 mL 18.5715 mL
5 mM 0.3714 mL 1.8571 mL 3.7143 mL
10 mM 0.1857 mL 0.9286 mL 1.8571 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molarity Calculator

  • Dilution Calculator

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

Mass
=
Concentration
×
Volume
×
Molecular Weight *

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

一般には略語で表示されます:C1V1 = C2V2

濃度 (開始)

C1

×
体積 (開始)

V1

=
濃度 (終了)

C2

×
体積 (終了)

V2

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

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Animal weight
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g

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(per animal)

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Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
純度とドキュメンテーション
参考文献

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.8571 mL 9.2857 mL 18.5715 mL 46.4287 mL
5 mM 0.3714 mL 1.8571 mL 3.7143 mL 9.2857 mL
10 mM 0.1857 mL 0.9286 mL 1.8571 mL 4.6429 mL
15 mM 0.1238 mL 0.6190 mL 1.2381 mL 3.0952 mL
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  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

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

質量   濃度   体積   分子量 *
= × ×

The dilution calculator equation

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

一般には略語で表示されます:C1V1 = C2V2

濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
× = ×
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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Inquiry Information

製品名:
Robustaflavone
製品番号:
HY-N5013
数量:
MCE 日本正規代理店: