| Weight | 352.434 g/mol |
|---|---|
| Formula | C21H24N2O3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Tetrahydroalstonine (6474-90-4)
ajmalicine · raubasine · 19-epiajmalicine
Score:
#2626 in Biochemistry
,
#5064 in Biology
,
#6544 in Chemistry
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- Formation of the Indole Alkaloids Serpentine and Ajmalicine in Cell Suspension Cultures of Catharanthus roseus (1977)
- Triadimefon induced changes in the antioxidant metabolism and ajmalicine production in Catharanthus roseus (L.) G. Don. (Plant Science, 2006)
- Stimulation of ajmalicine production and excretion from Catharanthus roseus: effects of adsorption in situ, elicitors and alginate immobilization (Applied Microbiology and Biotechnology, 1989)
- Pseudomonas fluorescens enhances biomass yield and ajmalicine production in Catharanthus roseus under water deficit stress (Colloids and Surfaces B: Biointerfaces, 2007)
- Water deficit stress effects on reactive oxygen metabolism in Catharanthus roseus; impacts on ajmalicine accumulation (Colloids and Surfaces B: Biointerfaces, 2008)
- Uptake and accumulation of ajmalicine into isolated vacuoles of cultured cells of Catharanthus roseus (L.) G. Don. and its conversion into serpentine (Planta, 1991)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - ajmalicine
- raubasine
- 19-epiajmalicine
- ajmalicine, (hydrochloride(19beta,20alpha))-isomer
- ajmalicine, (3-beta,19beta)-isomer
- ajmalicine, (19beta,20alpha)-isomer
- Lamuran
- ajmalicine, (19beta)-isomer
- tetrahydro-alstonine
- ajmalicine, (3beta,19alpha,20alpha)-isomer
- ajmalicine, PO4(19alpha)-isomer
- ajmalicine, hydrochloride(19alpha)-isomer
- ajmalicine, (19alpha,20alpha)-isomer
- delta-yohimbine
- akuammigine
- ajmalicine, (3beta,19alpha)-isomer
- rauvasan
-
SMILESCC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45
-
InChIKeyGRTOGORTSDXSFK-UHFFFAOYSA-N
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