
CAS Number80483-89-2
SynonymsCholest-5-ene-3|A,22-diol; 22R-hydroxycholesterol; (22R)-22-hydroxycholesterol; cholest-5-en-3beta,22-diol; 22S,23S-28-homobrassinolide; 22S,23S-homobrassinolide; 22(S)-hydroxycholesterol; Cholest-5-ene-3beta,22-diol; 22-Hydroxycholesterol; (22S)-22-Hydroxycholesterol; Isohomobrassinolide
Molecular FormulaC29H50O6
Molecular Weight494.70
Density1.1±0.1 g/cm3
Boiling Point643.0±55.0 °C at 760 mmHg
Melting Point193-194ºC
Appearancesolid
Symbol
Signal WordWarning
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 80483-89-2 |
| Catalog No. | 2A-2187300 |
| Chinese Name | 芸苔素内酯 |
| Synonyms | Cholest-5-ene-3|A,22-diol; 22R-hydroxycholesterol; (22R)-22-hydroxycholesterol; cholest-5-en-3beta,22-diol; 22S,23S-28-homobrassinolide; 22S,23S-homobrassinolide; 22(S)-hydroxycholesterol; Cholest-5-ene-3beta,22-diol; 22-Hydroxycholesterol; (22S)-22-Hydroxycholesterol; Isohomobrassinolide |
| Molecular Formula | C29H50O6 |
| Molecular Weight | 494.70 |
| Density | 1.1±0.1 g/cm3 |
| Boiling Point | 643.0±55.0 °C at 760 mmHg |
| Melting Point | 193-194ºC |
| Appearance | solid |
| Storage Condition | room temperature |
| Application | (22S,23S)-Homobrassinosteroid is one of the most active brassinosteroids inducing plant growth in various plant bioassay systems. (22S,23S)-homobrasinolide exhibits Akt-dependent anabolic activity in |
| PubChem ID | 24895446 |
| MDL Number | MFCD04973608 |
| SMILES | CCC(C(C)C)C(O)C(O)C(C)C1CCC2C3COC(=O)C4CC(O)C(O)CC4(C)C3CCC12C |
| InChI | InChI=1S/C29H50O6/c1-7-18(14(2)3)25(32)24(31)15(4)28-23-22(20-13-17(30)10-11-19(20)16(5)35-28)27(34)26(33)21-9-8-12-29(21,23)6/h14-16,18-28,31-34H,7-13H2,1-6H3/t15?,16-,18-,19+,20?,21?,22?,23?,24-,25-,26+,27-,28-,29-/m0/s1 |
| InChI Key | HJIKODJJEORHMZ-DNVPGCTHSA-N |
| NACRES Code | NA.77 |
| UNSPSC | 12352202 |
| Hazard Symbols | transportation |
| Bioactivity | (22S,23S)-Homobrassinolide is one of the most active brassinosteroids in inducing plant growth in various plant bioassay systems. (22S,23S)-Homobrassinolide shows Akt-dependent anabolic activity in rat skeletal muscle cells. Orally active[1]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Metabolic Disease In Vitro (22S,23S)-Homobrassinolide slightly stimulates ferricyanide reduction and promotes uptake of sucrose and alpha-aminoisobutyric acid [2]. References [1]. Esposito D, et al. Akt-dependent anabolic activity of natural and synthetic brassinosteroids in rat skeletal muscle cells. J Med Chem. 2011;54(12):4057-4066. [2]. Dahse I, et al. Effects of (22S,23S)-Homobrassinolide and Related Compounds on Membrane Potential and Transport of Egeria Leaf Cells. Plant Physiol. 1990;93(3):1268-1271. Chemical & Physical Properties Density 1.1±0.1 g/cm3 Boiling Point 643.0±55.0 °C at 760 mmHg Melting Point 193-194ºC Molecular Formula C29H50O6 Molecular Weight 494.704 Flash Point 203.2±25.0 °C Exact Mass 494.360748 PSA 107.22000 LogP 3.65 Vapour Pressure 0.0±4.3 mmHg at 25°C Index of Refraction 1.533 InChIKey HJIKODJJEORHMZ-DNVPGCTHSA-N SMILES CCC(C(C)C)C(O)C(O)C(C)C1CCC2C3COC(=O)C4CC(O)C(O)CC4(C)C3CCC12C |
| Use of | (22S,23S)-Homobrassinolide is one of the most active brassinosteroids in inducing plant growth in various plant bioassay systems. (22S,23S)-Homobrassinolide shows Akt-dependent anabolic activity in rat skeletal muscle cells. Orally active[1]. Properties Articles27 Name (2R,3S,22S,24S)-2,3,22,23-TETRAHYDROXY-24-ETHYL-β-HOMO-7-OXA-5A-CHOLESTAN-6-ONE Synonym More Synonyms Isohomobrassinolide Biological Activity Description (22S,23S)-Homobrassinolide is one of the most active brassinosteroids in inducing plant growth in various plant bioassay systems. (22S,23S)-Homobrassinolide shows Akt-dependent anabolic activity in rat skeletal muscle cells. Orally active[1]. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Metabolic Disease In Vitro (22S,23S)-Homobrassinolide slightly stimulates ferricyanide reduction and promotes uptake of sucrose and alpha-aminoisobutyric acid [2]. References [1]. Esposito D, et al. Akt-dependent anabolic activity of natural and synthetic brassinosteroids in rat skeletal muscle cells. J Med Chem. 2011;54(12):4057-4066. [2]. Dahse I, et al. Effects of (22S,23S)-Homobrassinolide and Related Compounds on Membrane Potential and Transport of Egeria Leaf Cells. Plant Physiol. 1990;93(3):1268-1271. Chemical & Physical Properties Molecular Formula C29H50O6 Exact Mass 494.360748 PSA 107.22000 Index of Refraction 1.533 InChIKey HJIKODJJEORHMZ-DNVPGCTHSA-N |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available |
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