erysodine
 
Notes:
None found
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CAS Number: 7290-03-1Picture of molecule3D/inchi
FDA UNII: 6WZ3T41Y11
Nikkaji Web: J15.487C
XlogP3-AA: 1.80 (est)
Molecular Weight: 299.36997000
Formula: C18 H21 N O3
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
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Google Scholar: with word "odor"Search
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Soluble in:
 water, 2953 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 erysodine usage levels up to:
 not for fragrance use.
 
Recommendation for erysodine flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 169017
National Institute of Allergy and Infectious Diseases: Data
 (2R,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-ol
Chemidplus: 0007290031
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References:
 (2R,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-ol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 169017
Pubchem (cas): 7290-03-1
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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
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB30255
FooDB: FDB002079
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
 erythrina fusca
Search Trop  Picture
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Synonyms:
(2R,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-ol
 erythrinan-16-ol, 1,2,6,7-tetradehydro-3,15-dimethoxy-, (3beta)-
1,2,6,7-tetradehydro-3,15-dimethoxyerythrinan-16-ol
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Articles:
PubMed: Bioassay-guided isolation of potent aphicidal Erythrina alkaloids against Aphis gossypii from the seed of Erythrina crista-galli L.
PubMed: Acetylcholine induces GABA release onto rod bipolar cells through heteromeric nicotinic receptors expressed in A17 amacrine cells.
PubMed: Functional expression of the α7 and α4-containing nicotinic acetylcholine receptors on the neonatal rat carotid body.
PubMed: Anti-HIV-1 and cytotoxicity of the alkaloids of Erythrina abyssinica Lam. growing in Sudan.
PubMed: Molecular determinants for competitive inhibition of alpha4beta2 nicotinic acetylcholine receptors.
PubMed: A new Erythrinan alkaloid from the seed of Erythrina addisoniae.
PubMed: High-performance liquid chromatography-mass spectrometric analysis of alkaloids extracted from seeds of Erythrina herbacea.
PubMed: Erythrinaline alkaloids and antimicrobial flavonoids from Erythrina latissima.
PubMed: Effects of the competitive nicotinic antagonist erysodine on behavior occasioned or maintained by nicotine: comparison with mecamylamine.
PubMed: Two novel glucodienoid alkaloids from Erythrina latissima seeds.
PubMed: Erysodine, a competitive antagonist at neuronal nicotinic acetylcholine receptors.
PubMed: Isolation of erysodine, erysotrine and hypaphorine from Erythrina suberosa Roxb. seeds.
PubMed: Erythrina alkaloids; studies on the constitution of erysodine erysovine and erysopine.
PubMed: Studies on Argentine plants; the alkaloids of Erythrina crista galli; chromatographic separation of erythratine and erysodine.
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