Daucosterol [474-58-8]

Katalog-Nummer HY-N0410-5mg

Size : 5mg

Marke : MedChemExpress


Beschreibung

Daucosterol is an orally active natural sterol compound, which has anti-inflammatory, anticancer and immunomodulatory activities. Daucosterol inhibits cancer cell proliferation by inducing autophagy through ROS-dependent manner. Daucosterol also inhibits colon cancer growth by inducing apoptosis, inhibiting cell migration and invasion and targeting caspase signalling pathway[1][2][3].

Cellular Effect
Cell Line Type Value Description References
A2780 IC50
>10 μg/mL
Compound: page 1629, R26C1
Cytotoxicity against human A2780 cells after 96 hrs by MTT assay
Cytotoxicity against human A2780 cells after 96 hrs by MTT assay
[PMID: 17125236]
A549 ED50
4.73 μg/mL
Compound: beta-sitosterol-beta-D-glucopyranoside
Cytotoxicity against human A549 cells after 7 days
Cytotoxicity against human A549 cells after 7 days
[PMID: 1453182]
A549 GI50
35.5 μM
Compound: 6
Growth inhibition of human A549 cells by MTT assay
Growth inhibition of human A549 cells by MTT assay
[PMID: 20153184]
A549 IC50
>10 μg/mL
Compound: page 1629, R26C1
Cytotoxicity against human A549 cells after 96 hrs by MTT assay
Cytotoxicity against human A549 cells after 96 hrs by MTT assay
[PMID: 17125236]
A549 IC50
>20 μg/mL
Compound: 10
Cytotoxicity against human A549 cells by MTT assay
Cytotoxicity against human A549 cells by MTT assay
[PMID: 22413887]
Bel-7402 IC50
>10 μg/mL
Compound: page 1629, R26C1
Cytotoxicity against human Bel-7402 cells after 96 hrs by MTT assay
Cytotoxicity against human Bel-7402 cells after 96 hrs by MTT assay
[PMID: 17125236]
BGC-823 IC50
>10 μg/mL
Compound: page 1629, R26C1
Cytotoxicity against human BGC-823 cells after 96 hrs by MTT assay
Cytotoxicity against human BGC-823 cells after 96 hrs by MTT assay
[PMID: 17125236]
Ca9-22 IC50
>20 μg/mL
Compound: 10
Cytotoxicity against human Ca9-22 cells by MTT assay
Cytotoxicity against human Ca9-22 cells by MTT assay
[PMID: 22413887]
HCT-8 IC50
>10 μg/mL
Compound: page 1629, R26C1
Cytotoxicity against human HCT8 cells after 96 hrs by MTT assay
Cytotoxicity against human HCT8 cells after 96 hrs by MTT assay
[PMID: 17125236]
Hep 3B2 IC50
>20 μg/mL
Compound: 10
Cytotoxicity against human Hep3B cells by MTT assay
Cytotoxicity against human Hep3B cells by MTT assay
[PMID: 22413887]
HepG2 IC50
>20 μg/mL
Compound: 10
Cytotoxicity against human HepG2 cells by MTT assay
Cytotoxicity against human HepG2 cells by MTT assay
[PMID: 22413887]
HL-60 GI50
50.8 μM
Compound: 6
Growth inhibition of human HL60 cells by MTT assay
Growth inhibition of human HL60 cells by MTT assay
[PMID: 20153184]
HT-1080 ED50
>100 μM
Compound: 15
Antiproliferative activity against human HT1080 cells by MTT assay
Antiproliferative activity against human HT1080 cells by MTT assay
[PMID: 11277741]
HT-29 ED50
0.444 μg/mL
Compound: beta-sitosterol-beta-D-glucopyranoside
Cytotoxicity against human HT-29 cells after 7 days
Cytotoxicity against human HT-29 cells after 7 days
[PMID: 1453182]
HT-29 ED50
4.44 x 10-1μg/mL
Compound: beta-sitosterol-beta-D-glucopyranoside
Cytotoxicity against human HT-29 cells after 7 days
Cytotoxicity against human HT-29 cells after 7 days
[PMID: 1453182]
HT-29 GI50
46.8 μM
Compound: 6
Growth inhibition of human HT-29 cells by MTT assay
Growth inhibition of human HT-29 cells by MTT assay
[PMID: 20153184]
HUVEC ED50
>5 μg/mL
Compound: beta-sitosterol glucoside
Cytotoxicity against HUVEC
Cytotoxicity against HUVEC
[PMID: 15043409]
LNCaP ED50
>5 μg/mL
Compound: beta-sitosterol glucoside
Cytotoxicity against human LNCAP cells
Cytotoxicity against human LNCAP cells
[PMID: 15043409]
Lu1 ED50
>5 μg/mL
Compound: beta-sitosterol glucoside
Cytotoxicity against human Lu1 cells
Cytotoxicity against human Lu1 cells
[PMID: 15043409]
MCF7 ED50
>5 μg/mL
Compound: beta-sitosterol glucoside
Cytotoxicity against human MCF7 cells
Cytotoxicity against human MCF7 cells
[PMID: 15043409]
MCF7 ED50
44.39 μg/mL
Compound: beta-sitosterol-beta-D-glucopyranoside
Cytotoxicity against human MCF7 cells after 7 days
Cytotoxicity against human MCF7 cells after 7 days
[PMID: 1453182]
MCF7 IC50
>20 μg/mL
Compound: 10
Cytotoxicity against human MCF7 cells by MTT assay
Cytotoxicity against human MCF7 cells by MTT assay
[PMID: 22413887]
MDA-MB-231 IC50
>20 μg/mL
Compound: 10
Cytotoxicity against human MDA-MB-231 cells by MTT assay
Cytotoxicity against human MDA-MB-231 cells by MTT assay
[PMID: 22413887]
NCI-H460 IC50
>50 μM
Compound: 3
Cytotoxicity against human NCI-H460 cells incubated for 24 hrs by MTT assay
Cytotoxicity against human NCI-H460 cells incubated for 24 hrs by MTT assay
[PMID: 28606759]
P388 ED50
53 μg/mL
Compound: Beta-sitosterol glycoside
Cytotoxicity against mouse P388 cells
Cytotoxicity against mouse P388 cells
[PMID: 3404159]
RAW264.7 IC50
77.4 μM
Compound: 116
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production
[PMID: 31255927]
SK-OV-3 GI50
29.8 μM
Compound: 6
Growth inhibition of human SKOV3 cells by MTT assay
Growth inhibition of human SKOV3 cells by MTT assay
[PMID: 20153184]
In Vitro

Daucosterol (0.01-100 μM, 48 h) inhibits the proliferation of MCF-7, AGS, MGC803 and BGC823 cells in a dose-dependent manner, with IC50s of 19.96 μM, 3.13 μM, 24.19 μM and 16.95 μM, respectively[1].
Daucosterol (50 μM, 24 h) significantly increases ROS production in MCF-7 and BGC823 cells[1].
Daucosterol (0-80 μM, 48 h) inhibits proliferation and promotes apoptosis in PC3 and LNCap cells[2].

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

Western Blot Analysis[2]

Cell Line: PC3 and LNCap cells
Concentration: 0-80 μM
Incubation Time: 48 h
Result: Increased the expressions of cleaved caspase 3, cleaved caspase 9, Bax protein, LC3II/LC3I ration and Beclin 1.
Decreased the the expressions of Bax protein and p62.
In Vivo

Daucosterol (0.5-2.5 mg/kg, p.o., once per day for 7 days) significantly inhibits the H22 tumor growth in ICR mice inoculated with H22 hepatoma cells[1].

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

Molekulargewicht

576.85

Formel

C35H60O6

CAS. Nr.
Appearance

Solid

Color

White to off-white

SMILES

C[C@H](CC[C@@H](CC)C(C)C)[C@](CC1)(15)[C@]2(C)[C@]1(15)[C@]([C@]3(15)CC2)(15)CC=C([C@]3(C)CC4)C[C@H]4O[C@@]5(15)[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O5

Structure Classification
Initial Source
Versand

Room temperature in continental US; may vary elsewhere.

Speicherung
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 2 years
-20°C 1 year
Lösungsmittel & Löslichkeit
In Vitro: 

DMSO : 3.33 mg/mL (5.77 mM; Need ultrasonic; 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 1.7336 mL 8.6678 mL 17.3355 mL
5 mM 0.3467 mL 1.7336 mL 3.4671 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.

  • Molaritätsrechner

  • Verdünnungsrechner

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

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

This equation is commonly abbreviated as: C1V1 = C2V2

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
Reinheit & Dokumentation
Verweise

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Katalog-Nummer
Beschreibung
Cond.
Preis zzgl. MwSt.
A10867-1000
 1g 
A10867-5000
 5g