| Weight | 354.45 g/mol |
|---|---|
| Formula | C21H26N2O3 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Isovincamine (6835-99-0)
Vincamine · Vincapront · Devincan
Score:
#545 in Neuroscience
,
#929 in Biochemistry
,
#2464 in Biology
,
#3072 in Chemistry
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- Disposition Kinetics and Oral Bioavailability of Vincamine-Loaded Polyalkyl Cyanoacrylate Nanoparticles (Journal of Pharmaceutical Sciences, 1986)
- An efficient and practical total synthesis of (+)-vincamine from L-aspartic acid (Journal of Organic Chemistry, 1990)
- The Total Synthesis of Vincamine (Journal of the American Chemical Society, 1964)
- Reactions with indole derivatives-LV. : An enantiodivergent route to both vincamine enantiomers (Tetrahedron, 1983)
- Therapeutic efficacy of vincamine in dementia (Neuropsychobiology, 1996)
- Effects of aging and vincamine derivatives on pericapillary microenvironment: stereological characterization of the cerebral capillary network. (Neurobiology of Aging, 1990)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Vincamine
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-
SMILESCCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)(C(=O)OC)O
-
InChIKeyRXPRRQLKFXBCSJ-UHFFFAOYSA-N
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