BRASSININ
- CAS NO.：105748-59-2
- Empirical Formula: C11H12N2S2
- Molecular Weight: 236.36
- MDL number: MFCD01632490
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-05-18 11:31:17
What is BRASSININ?
Chemical properties
Off-White to Pale Yellow Solid
The Uses of BRASSININ
Brassinin is a plant metabolite of great significance due to its dual role both as an effective phytoalexin and as an early biosynthetic precursor of the majority of the phytoalexins produced by plants of the family Brassicaceae (Cruciferae).
The Uses of BRASSININ
A biosynthetic precursor of Brassilexin
What are the applications of Application
Brassinin is An effective inhibitor against two stage skin carcinogenesis. An inducer of Phase II enzymes and inhibitor of chemically induced carcinogenesis
Definition
ChEBI: Brassinin is a dithiocarbamic ester and an indole phytoalexin.
Properties of BRASSININ
| Melting point: | 142-144°C |
| storage temp. | -20°C Freezer, Under Inert Atmosphere |
| solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly, Heated) |
| form | Solid |
| color | Off-White to Pale Yellow |
Safety information for BRASSININ
Computed Descriptors for BRASSININ
New Products
Tubulysin C Tubulysin G 2,2-diethoxyethanethioamide Tubulysin E Tubulysin I Tubulysin F Potassium HMDS (1.0 M in THF) 3-METHYLAZETIDIN-3-OL HYDROCHLORIDE 2,2,6,6-tetramethyl-2H-3,5,6-trihydropyran-4-one tetrahydro-4-methyl-2H-pyran 4-(Benzyloxy)-3-bromophenylacetic Acid Isoxazole, 3-[[[5-(difluoromethoxy)-1-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]methyl]thio]-4,5-dihydro-5,5-dimethyl- Cyclobutanamine, 3,3-difluoro- (9CI) (2,3-Dihydro- benzofuran-5-yl)- ethanol (6-Nitro-2,3- dichlorobenzylamino) acetic acid ethylester.HCl 2-Bromo-6- nitroanisole Magnesium Trisilicate Lubiprostone Latanoprostene Bunod 1H-Imidazole-4-carbonitrile 7-Methoxyquinoline-4-carboxylic acid 7-Methoxyquinoline-4-carbonitrile Montelukast (3S)-Hydroxy Benzoate Sertraline EP Impurity G / Sertraline BP Impurity G / Sertraline Enantiomer / Sertraline (1R,4R)-cis-IsomerRelated products of tetrahydrofuran
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