Campesterol structure
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Common Name | Campesterol | ||
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CAS Number | 474-62-4 | Molecular Weight | 400.680 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 489.5±14.0 °C at 760 mmHg | |
Molecular Formula | C28H48O | Melting Point | 156-160ºC | |
MSDS | Chinese USA | Flash Point | 214.3±12.4 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of CampesterolCampesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. |
Name | campesterol |
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Synonym | More Synonyms |
Description | Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. |
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Related Catalog | |
In Vitro | Campesterol shows a weak cytotoxicity in non-proliferating human umbilical vein endothelial cells (HUVECs). Within the non-cytotoxic concentration range, campesterol significantly inhibits the bFGF-induced proliferation and tube formation of HUVECs in a concentration-dependent manner, while it does not affect the motility of HUVECs. 50 μg/mL of campesterol decreases the cell viability up to about 56% of control(IC50 of over 50 μg/mL)[1]. |
In Vivo | Campesterol effectively disrupts the bFGF-induced neovascularization in chick chorioallantoic membrane (CAM) in vivo[1]. |
Cell Assay | The effect of campesterol on the viable cell number was assessed by XTT assay. HUVECs were treated with various concentrations (10, 20, 30, 40 and 50 μg/mL) of campesterol and incubated at 37 °C in a humidified incubator for 24 h, a XTT working solution was added to each well. The cells were incubated at 37 °C for 2 h and the optical density was measured using a microplate reader at 450 nm[1]. |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 489.5±14.0 °C at 760 mmHg |
Melting Point | 156-160ºC |
Molecular Formula | C28H48O |
Molecular Weight | 400.680 |
Flash Point | 214.3±12.4 °C |
Exact Mass | 400.370514 |
PSA | 20.23000 |
LogP | 10.20 |
Vapour Pressure | 0.0±2.8 mmHg at 25°C |
Index of Refraction | 1.522 |
Storage condition | -20°C |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H312-H315-H319-H332-H335 |
Precautionary Statements | P261-P280-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn: Harmful;T: Toxic; |
Risk Phrases | R20/21/22 |
Safety Phrases | 26-36-45-36/37/39-23 |
RIDADR | UN 1888 6.1/PG 3 |
Phytochemical Characterization of Veronica officinalis L., V. teucrium L. and V. orchidea Crantz from Romania and Their Antioxidant and Antimicrobial Properties.
Int. J. Mol. Sci. 16 , 21109-27, (2015) Aerial parts of Veronica species are used in Romanian traditional medicine for the treatment of various conditions like kidney diseases, cough, and catarrh, and are known for their wound-healing prope... |
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Sterol Composition in Infant Formulas and Estimated Intake.
J. Agric. Food Chem. 63 , 7245-51, (2015) Sterol contents in infant formulas (IFs) from the European market were determined, and their intakes by infants between 0 and 6 months were evaluated. Total animal sterols (mg/100 mL) ranged from 1.71... |
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On-line liquid chromatography-gas chromatography: A novel approach for the analysis of phytosterol oxidation products in enriched foods.
J. Chromatogr. A. 1396 , 98-108, (2015) A novel methodology for the automated qualitative and quantitative determination of phytosterol oxidation products in enriched foods via on-line liquid chromatography-gas chromatography (LC-GC) was es... |
Ergost-5-en-3β-ol, (24R)- |
(24R)-Ergost-5-en-3b-ol |
(24R)-5-Ergosten-3β-ol |
EINECS 207-484-4 |
(3β,24R)-Ergost-5-en-3-ol |
(24R)-5-Ergosten-3-β-ol |
(3b,24R)-Ergost-5-en-3-ol |
MFCD00010475 |
(24R)-Ergost-5-en-3β-ol |
(24R)-5-Ergosten-3b-ol |
Ergost-5-en-3-ol, (3β)- |
Ergost-5-en-3β-ol |
Campesterol |
(24R)-Ergost-5-en-3-β-ol |
(3β)-Ergost-5-en-3-ol |
Ergost-5-en-3-β-ol |
Ergost-5-en-3-ol, (3β,24R)- |