BRASSICASTEROL structure, CAS 474-67-9

BRASSICASTEROL

CAS Number474-67-9

SynonymsEINECS 207-486-5; Ergosta-5,22-dien-3β-ol; (3β,22E)-Ergosta-5,22-dien-3-ol

Molecular FormulaC28H46O

Molecular Weight398.664

Purity98.00%

Density1.0±0.1 g/cm3

Boiling Point488.7±14.0 °C at 760 mmHg

Melting Point

Flash Point

Appearance

EINECS

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Symbol

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Cat. No.: 2A-1172148 Purity: 98.00%
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Quality Control of [ 474-67-9 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number474-67-9
Catalog No.2A-1172148
Chinese Name菜籽甾醇
SynonymsEINECS 207-486-5; Ergosta-5,22-dien-3β-ol; (3β,22E)-Ergosta-5,22-dien-3-ol
Molecular FormulaC28H46O
Molecular Weight398.664
Purity98.00
Density1.0±0.1 g/cm3
Boiling Point488.7±14.0 °C at 760 mmHg
Storage ConditionStore sealed at 2-8°C, placed in a ventilated, dry
ApplicationBrassinosterol is a metabolite of ergosterol and plays a role in inhibiting the development and promotion of bladder cancer through androgen signaling [1]. Brassinosterol has dual anti-infectious prop
PubChem ID11006
SMILESCC(C)C(C)C=CC(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C
InChIInChI=1S/C28H46O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-9,18-20,22-26,29H,10-17H2,1-6H3/b8-7+/t19-,20+,22-,23-,24+,25-,26-,27-,28+/m0/s1
InChI KeyOILXMJHPFNGGTO-ZAUYPBDWSA-N
MSDSmsds/172372_2_474_67_9.pdf
BioactivityBrassicasterol, a metabolite of Ergosterol, plays a role in the inhibitory effect on bladder carcinogenesis promotion via androgen signaling[1]. Brassicasterol shows dual anti-infective properties against HSV-1 (IC50=1.2 µM) and Mycobacterium tuberculosis, and cardiovascular protective effect[2]. Brassicasterol exerts an anti-cancer effect by dual-targeting AKT and androgen receptor signaling in prostate cancer[3]. Related Catalog Research Areas >> Cancer Signaling Pathways >> Anti-infection >> HSV Research Areas >> Infection Signaling Pathways >> Others >> Androgen Receptor Signaling Pathways >> Anti-infection >> Bacterial References [1]. Yasuharu Yazawa, et al. Inhibitory effect of ergosterol on bladder carcinogenesis is due to androgen signaling inhibition by brassicasterol, a metabolite of ergosterol. J Nat Med. 2020 Sep;74(4):680-688. [2]. Sherif T S Hassan. Brassicasterol with Dual Anti-Infective Properties against HSV-1 and Mycobacterium tuberculosis, and Cardiovascular Protective Effect: Nonclinical In Vitro and In Silico Assessments. Biomedicines. 2020 May 24;8(5):132. [3]. Yinzhu Xu, et al. Brassicasterol from Edible Aquacultural Hippocampus abdominalis Exerts an Anti-Cancer Effect by Dual-Targeting AKT and AR Signaling in Prostate Cancer. Biomedicines. 2020 Sep 22;8(9):370. Chemical & Physical Properties Density 1.0±0.1 g/cm3 Boiling Point 488.7±14.0 °C at 760 mmHg Molecular Formula C28H46O Molecular Weight 398.664 Flash Point 213.3±12.4 °C Exact Mass 398.354858 PSA 20.23000 LogP 9.68 Vapour Pressure 0.0±2.8 mmHg at 25°C Index of Refraction 1.532 InChIKey OILXMJHPFNGGTO-ZAUYPBDWSA-N SMILES CC(C)C(C)C=CC(C)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C Storage condition 2-8°C
Use ofBrassicasterol, a metabolite of Ergosterol, plays a role in the inhibitory effect on bladder carcinogenesis promotion via androgen signaling[1]. Brassicasterol shows dual anti-infective properties against HSV-1 (IC50=1.2 µM) and Mycobacterium tuberculosis, and cardiovascular protective effect[2]. Brassicasterol exerts an anti-cancer effect by dual-targeting AKT and androgen receptor signaling in prostate cancer[3]. Properties Name Brassicasterol Synonym More Synonyms Ergosta-5,22-dien-3β-ol Biological Activity Description Brassicasterol, a metabolite of Ergosterol, plays a role in the inhibitory effect on bladder carcinogenesis promotion via androgen signaling[1]. Brassicasterol shows dual anti-infective properties against HSV-1 (IC50=1.2 µM) and Mycobacterium tuberculosis, and cardiovascular protective effect[2]. Brassicasterol exerts an anti-cancer effect by dual-targeting AKT and androgen receptor signaling in prostate cancer[3]. Related Catalog Research Areas >> Cancer Signaling Pathways >> Anti-infection >> HSV Research Areas >> Infection Signaling Pathways >> Others >> Androgen Receptor Signaling Pathways >> Anti-infection >> Bacterial References [1]. Yasuharu Yazawa, et al. Inhibitory effect of ergosterol on bladder carcinogenesis is due to androgen signaling inhibition by brassicasterol, a metabolite of ergosterol. J Nat Med. 2020 Sep;74(4):680-688. [2]. Sherif T S Hassan. Brassicasterol with Dual Anti-Infective Properties against HSV-1 and Mycobacterium tuberculosis, and Cardiovascular Protective Effect: Nonclinical In Vitro and In Silico Assessments. Biomedicines. 2020 May 24;8(5):132. [3]. Yinzhu Xu, et al. Brassicasterol from Edible Aquacultural Hippocampus abdominalis Exerts an Anti-Cancer Effect by Dual-Targeting AKT and AR Signaling in Prostate Cancer. Biomedicines. 2020 Sep 22;8(9):370. Chemical & Physical Properties Molecular Formula C28H46O Exact Mass 398.354858 PSA 20.23000 Index of Refraction 1.532 InChIKey OILXMJHPFNGGTO-ZAUYPBDWSA-N
Transport InfoProduct name: Rapeseed sterol
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