Nintedanib [656247-17-5]

Referência HY-50904-100mg

Tamanho : 100mg

Marca : MedChemExpress

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Description

Nintedanib (BIBF 1120) is a potent triple angiokinase inhibitor for VEGFR1/2/3, FGFR1/2/3 and PDGFRα/β with IC50s of 34 nM/13 nM/13 nM, 69 nM/37 nM/108 nM and 59 nM/65 nM, respectively.

IC50 & Target[1]

VEGFR1

34 nM (IC50)

VEGFR2

13 nM (IC50)

VEGFR3

13 nM (IC50)

FGFR1

69 nM (IC50)

FGFR2

37 nM (IC50)

FGFR3

108 nM (IC50)

PDGFRα

59 nM (IC50)

PDGFRβ

65 nM (IC50)

Cellular Effect
Cell Line Type Value Description References
A549 IC50
22.62 μM
Compound: Nintedanib
Antiproliferative activity against human A549 cells after 72 hrs by MTT assay
Antiproliferative activity against human A549 cells after 72 hrs by MTT assay
[PMID: 28826084]
Calu-6 EC50
>1 μM
Compound: 3, BIBF1120
Antiangiogenic activity against human Calu6 cells assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay
Antiangiogenic activity against human Calu6 cells assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay
[PMID: 19522465]
Calu-6 EC50
>3500 nM
Compound: BIBF 1120
Antiangiogenic activity in human Calu6 assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay in presence of fetal calf serum
Antiangiogenic activity in human Calu6 assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay in presence of fetal calf serum
[PMID: 18559524]
FaDu EC50
>1 μM
Compound: 3, BIBF1120
Antiangiogenic activity against human FADU cells assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay
Antiangiogenic activity against human FADU cells assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay
[PMID: 19522465]
FaDu EC50
>4500 nM
Compound: BIBF 1120
Antiangiogenic activity in human FADU assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay in presence of fetal calf serum
Antiangiogenic activity in human FADU assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay in presence of fetal calf serum
[PMID: 18559524]
HeLa EC50
>1 μM
Compound: 3, BIBF1120
Antiangiogenic activity against human HeLa cells assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay
Antiangiogenic activity against human HeLa cells assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay
[PMID: 19522465]
HeLa EC50
>3500 nM
Compound: BIBF 1120
Antiangiogenic activity in human HeLa assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay in presence of fetal calf serum
Antiangiogenic activity in human HeLa assessed as inhibition of cell proliferation by [3H]thymidine incorporation assay in presence of fetal calf serum
[PMID: 18559524]
HeLa IC50
51.65 μM
Compound: Nintedanib
Antiproliferative activity against human HeLa cells after 72 hrs by MTT assay
Antiproliferative activity against human HeLa cells after 72 hrs by MTT assay
[PMID: 28190652]
HT-29 IC50
0.83 μM
Compound: Nintedanib
Antiproliferative activity against human HT-29 cells after 72 hrs by MTT assay
Antiproliferative activity against human HT-29 cells after 72 hrs by MTT assay
[PMID: 28826084]
HT-29 IC50
4.9 μM
Compound: Nintedanib
Antiproliferative activity against human HT-29 cells after 72 hrs by MTT assay
Antiproliferative activity against human HT-29 cells after 72 hrs by MTT assay
[PMID: 28190652]
HUVEC EC50
<10 nM
Compound: BIBF 1120
Antiangiogenic activity in HUVEC assessed as inhibition of VEGF-induced apoptosis by [3H]thymidine incorporation assay
Antiangiogenic activity in HUVEC assessed as inhibition of VEGF-induced apoptosis by [3H]thymidine incorporation assay
[PMID: 18559524]
HUVEC EC50
290 nM
Compound: BIBF 1120
Antiangiogenic activity in HUVEC assessed as inhibition of bFGF-induced cell proliferation by [3H]thymidine incorporation assay
Antiangiogenic activity in HUVEC assessed as inhibition of bFGF-induced cell proliferation by [3H]thymidine incorporation assay
[PMID: 18559524]
HUVEC EC50
9 nM
Compound: BIBF 1120
Antiangiogenic activity in HUVEC assessed as inhibition of VEGF-induced cell proliferation by [3H]thymidine incorporation assay
Antiangiogenic activity in HUVEC assessed as inhibition of VEGF-induced cell proliferation by [3H]thymidine incorporation assay
[PMID: 18559524]
HUVEC IC50
10 nM
Compound: 3, BIBF1120
Antiangiogenic activity in HUVEC assessed as inhibition of VEGF-induced cell proliferation by [3H]thymidine incorporation assay
Antiangiogenic activity in HUVEC assessed as inhibition of VEGF-induced cell proliferation by [3H]thymidine incorporation assay
[PMID: 19522465]
MCF7 IC50
8.28 μM
Compound: Nintedanib
Antiproliferative activity against human MCF7 cells after 72 hrs by MTT assay
Antiproliferative activity against human MCF7 cells after 72 hrs by MTT assay
[PMID: 28826084]
NIH3T3 IC50
2.41 μM
Compound: Nintedanib
Antiproliferative activity against mouse NIH3T3 cells assessed as cell growth inhibition incubated for 24 to 72 hrs by CCK-8 assay
Antiproliferative activity against mouse NIH3T3 cells assessed as cell growth inhibition incubated for 24 to 72 hrs by CCK-8 assay
[PMID: 36463728]
NRK-49F IC50
1.1 μM
Compound: 2
Inhibition of TGF-beta-induced collagen accumulation in rat NRK-49F cells incubated for 2 days by PSR staining based microscopic analysis
Inhibition of TGF-beta-induced collagen accumulation in rat NRK-49F cells incubated for 2 days by PSR staining based microscopic analysis
[PMID: 31699535]
NRK-49F IC50
1.1 μM
Compound: Nintedanib
Inhibition of TGF-beta-induced collagen accumulation in rat NRK-49F cells incubated for 2 days by PSR staining based microscopic analysis
Inhibition of TGF-beta-induced collagen accumulation in rat NRK-49F cells incubated for 2 days by PSR staining based microscopic analysis
[PMID: 32334267]
PC-3 IC50
<30 μM
Compound: Nintedanib
Cytotoxicity against human PC3 cells assessed as reduction in cell viability by CellTiter-Fluor assay
Cytotoxicity against human PC3 cells assessed as reduction in cell viability by CellTiter-Fluor assay
[PMID: 30951312]
Sf9 IC50
1.9 nM
Compound: BIBF 1120
Inhibition of N-terminal GST-tagged human recombinant PDGFRalpha D842I mutant expressed in baculovirus-infected Sf9 cells using FAM-labeled peptide and ATP as substrate preincubated for 10 mins followed by substrate addition measured after 1 hr by mobilit
Inhibition of N-terminal GST-tagged human recombinant PDGFRalpha D842I mutant expressed in baculovirus-infected Sf9 cells using FAM-labeled peptide and ATP as substrate preincubated for 10 mins followed by substrate addition measured after 1 hr by mobilit
[PMID: 32305182]
Sf9 IC50
13 nM
Compound: BIBF 1120
Inhibition of mouse GST-fused VEGFR2 expressed in Sf9 insect cells after 20 mins by scintillation counting
Inhibition of mouse GST-fused VEGFR2 expressed in Sf9 insect cells after 20 mins by scintillation counting
[PMID: 18559524]
Sf9 IC50
21 nM
Compound: BIBF 1120
Inhibition of human GST-fused VEGFR2 expressed in Sf9 insect cells after 20 mins by scintillation counting
Inhibition of human GST-fused VEGFR2 expressed in Sf9 insect cells after 20 mins by scintillation counting
[PMID: 18559524]
Sf9 IC50
5 nM
Compound: 3, BIBF1120
Inhibition of human VEGFR2 expressed in Sf9 cells
Inhibition of human VEGFR2 expressed in Sf9 cells
[PMID: 19522465]
SK-OV-3 IC50
28.76 μM
Compound: Nintedanib
Antiproliferative activity against human SKOV3 cells after 72 hrs by MTT assay
Antiproliferative activity against human SKOV3 cells after 72 hrs by MTT assay
[PMID: 28190652]
In Vitro

Nintedanib (BIBF 1120) binds to the ATP-binding site in the cleft between the amino and carboxy terminal lobes of the kinase domain. Nintedanib (BIBF 1120) inhibits proliferation of PDGF-BB stimulated BRPs with EC50 of 79 nM in cell assays. Nintedanib (BIBF 1120) (100 nM) blocks activation of MAPK after stimulation with 5% serum plus PDGF-BB. Nintedanib (BIBF 1120) prevents PDGF-BB stimulated proliferation with an EC50 of 69 nM in cultures of human vascular smooth muscle cells (HUASMC)[1].

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

Solvant et solubilité
In Vitro: 

DMSO : 5 mg/mL (9.27 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

H2O : < 0.1 mg/mL (insoluble)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.8532 mL 9.2658 mL 18.5316 mL
5 mM 0.3706 mL 1.8532 mL 3.7063 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  50% PEG300    50% Saline

    Solubility: 10 mg/mL (18.53 mM); Suspended solution; Need ultrasonic

  • Protocol 2

    Add each solvent one by one:  1% CMC/0.5% Tween-80 in Saline water

    Solubility: 10 mg/mL (18.53 mM); Suspended solution; Need ultrasonic

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

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
Pureté et documentation
Références

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Referência
Descrição
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Price Bef. VAT
9042-05
 1.0mL