6-deoxocastasterone
campestan-2alpha,3alpha,22R,23R-tetrol
 
Notes:
None found
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CAS Number: 87833-54-3Picture of molecule3D/inchi
Nikkaji Web: J146.605D
XlogP3: 6.30 (est)
Molecular Weight: 450.70330000
Formula: C28 H50 O4
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 0.07423 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
 None found
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for 6-deoxocastasterone usage levels up to:
 not for fragrance use.
 
Recommendation for 6-deoxocastasterone flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
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EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 13870433
National Institute of Allergy and Infectious Diseases: Data
 (2R,3S,5S,8R,9S,10S,13S,14S,17R)-17-[(2S,3R,4R,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-2,3-diol
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References:
 (2R,3S,5S,8R,9S,10S,13S,14S,17R)-17-[(2S,3R,4R,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-2,3-diol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 13870433
Pubchem (cas): 87833-54-3
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
KEGG (GenomeNet): C15802
HMDB (The Human Metabolome Database): HMDB33984
FooDB: FDB012216
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 camellia sinensis
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 cupressus arizonica pollen
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 phaseolus vulgaris
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 terminalia chebula
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Synonyms:
 campestan-2alpha,3alpha,22R,23R-tetrol
(2R,3S,5S,8R,9S,10S,13S,14S,17R)-17-[(2S,3R,4R,5S)-3,4-dihydroxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-2,3-diol
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Articles:
PubMed: Overexpression of Arabidopsis thaliana brassinosteroid-related acyltransferase 1 gene induces brassinosteroid-deficient phenotypes in creeping bentgrass.
PubMed: Occurrence of brassinosteroids in non-flowering land plants, liverwort, moss, lycophyte and fern.
PubMed: Effects of 24-epibrassinolide and green light on plastid gene transcription and cytokinin content of barley leaves.
PubMed: Mild Potassium Chloride Stress Alters the Mineral Composition, Hormone Network, and Phenolic Profile in Artichoke Leaves.
PubMed: Homeostasis of brassinosteroids regulated by DRL1, a putative acyltransferase in Arabidopsis.
PubMed: Arabidopsis PIZZA has the capacity to acylate brassinosteroids.
PubMed: BAT1, a putative acyltransferase, modulates brassinosteroid levels in Arabidopsis.
PubMed: Isolation and characterization of brassinosteroids from algal cultures of Chlorella vulgaris Beijerinck (Trebouxiophyceae).
PubMed: Castasterone is a likely end product of brassinosteroid biosynthetic pathway in rice.
PubMed: Characterization of two brassinosteroid C-6 oxidase genes in pea.
PubMed: Tomato cytochrome P450 CYP734A7 functions in brassinosteroid catabolism.
PubMed: Brassinosteroids are inherently biosynthesized in the primary roots of maize, Zea mays L.
PubMed: shk1-D, a dwarf Arabidopsis mutant caused by activation of the CYP72C1 gene, has altered brassinosteroid levels.
PubMed: The last reaction producing brassinolide is catalyzed by cytochrome P-450s, CYP85A3 in tomato and CYP85A2 in Arabidopsis.
PubMed: Brassinosteroid deficiency due to truncated steroid 5alpha-reductase causes dwarfism in the lk mutant of pea.
PubMed: Cytochrome P450-catalyzed brassinosteroid pathway activation through synthesis of castasterone and brassinolide in Phaseolus vulgaris.
PubMed: Hormone levels and response during de-etiolation in pea.
PubMed: Synthesis and biological activity of 26-norbrassinolide, 26-norcastasterone and 26-nor-6-deoxocastasterone.
PubMed: Brassinosteroid-6-oxidases from Arabidopsis and tomato catalyze multiple C-6 oxidations in brassinosteroid biosynthesis.
PubMed: Accumulation of 6-deoxocathasterone and 6-deoxocastasterone in Arabidopsis, pea and tomato is suggestive of common rate-limiting steps in brassinosteroid biosynthesis.
PubMed: Brassinosteroid levels increase drastically prior to morphogenesis of tracheary elements.
PubMed: Biosynthetic pathways of brassinolide in Arabidopsis.
PubMed: Biosynthesis of brassinosteroids in cultured cells of Catharanthus roseus.
PubMed: The tomato DWARF enzyme catalyses C-6 oxidation in brassinosteroid biosynthesis.
PubMed: Brassinosteroids in Arabidopsis thaliana.
PubMed: Blockage of Brassinosteroid Biosynthesis and Sensitivity Causes Dwarfism in Garden Pea.
PubMed: Identification of castasterone, 6-deoxocastasterone, typhasterol and 6-deoxotyphasterol from the shoots of Arabidopsis thaliana.
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