| Weight | 354.45 g/mol |
|---|---|
| Formula | C21H26N2O3 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
vincamine (1617-90-9)
Vincapront · Devincan · Pervincamine
Score:
#506 in Neuroscience
,
#878 in Biochemistry
,
#2350 in Biology
,
#2913 in Chemistry
"What do you need help with?"
LabBot
- Sigma-Aldrich - vincamine81.90 - 125.50 USD
- Fisher Scientific - Search for vincamine
- TCI - Search for vincamine
- 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. - Vincapront
- Devincan
- Pervincamine
- Cerebroxine
- Vincimax
-
SMILESCCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)(C(=O)OC)O
-
InChIKeyRXPRRQLKFXBCSJ-UHFFFAOYSA-N
- Pubchem - vincamine
- Wikipedia - vincamine
Vincamine is a monoterpenoid indole alkaloid found in the leaves of Vinca minor (lesser periwinkle), comprising about 25-65% of the indole alkaloids found in Vinca minor by weight. It can be synthesized from related alkaloids.
Suppliers
Most-cited Publications
Areas of Application
Safety
Trends
Alternate Names
External Links
Similar Compounds
Acequinocyl
(57960-19-7)
6 alternate names
3 safety hazards
3 suppliers
BENZILIC ACID
(76-93-7)
6 alternate names
1 safety hazard
3 suppliers
Tetrahydrodeoxycorticosterone
(567-03-3, 567-02-2)
6 alternate names
3 suppliers
BUTACHLOR
(23184-66-9)
6 alternate names
5 safety hazards
3 suppliers
2-DODECYLBENZENESULFONIC ACID
(47221-31-8, 27176-87-0, 68584-22-5, 85536-14-7, 27176-87-0)
6 alternate names
3 suppliers
Methyl ricinoleate
(141-24-2)
6 alternate names
3 suppliers
methyl 12-hydroxyoctadec-9-enoate
(141-24-2)
6 alternate names
3 suppliers
Cinchophen
(132-60-5)
6 alternate names
3 suppliers
Sultopride
(53583-79-2)
6 alternate names
3 suppliers
2-METHOXYESTRONE
(362-08-3)
6 alternate names
3 suppliers
53-00-9
(53-00-9)
6 alternate names
3 suppliers
Methyl 12-hydroxyoctadecanoate
(141-23-1)
6 alternate names
3 suppliers
6052-68-2
(42438-90-4, 6052-68-2)
6 alternate names
3 suppliers
Benzo[b]fluoranthene
(205-99-2)
6 alternate names
2 safety hazards
3 suppliers
ERUCIC ACID
(1072-39-5, 112-86-7)
6 alternate names
3 suppliers
N,N'-Diacetylbenzidine
(613-35-4)
6 alternate names
4 safety hazards
3 suppliers
Ethylan
(72-56-0)
6 alternate names
3 suppliers
12-Hydroxystearic acid
(106-14-9, 36377-33-0, 18417-00-0, 27924-99-8, 5762-36-7)
6 alternate names
3 suppliers
Phenmedipham
(13684-63-4)
6 alternate names
3 safety hazards
3 suppliers
ZEARALENONE
(17924-92-4, 36455-70-6)
6 alternate names
3 suppliers
CP 47497
(70434-82-1)
6 alternate names
3 suppliers
ZERANOL
(26538-44-3, 55331-29-8)
6 alternate names
3 suppliers
2-HYDROXYESTRONE
(362-06-1)
6 alternate names
3 suppliers
retinal
(116-31-4)
6 alternate names
3 suppliers
Milrinone lactate
(100286-97-3)
6 alternate names
3 suppliers
FLUENETIL
(4301-50-2)
6 alternate names
1 safety hazard
3 suppliers
Amineptine
(57574-09-1)
6 alternate names
3 suppliers
9-cis-Retinal
(514-85-2)
6 alternate names
3 suppliers
Methenamine hippurate
(5714-73-8)
6 alternate names
3 suppliers
hydroquinidine
(1435-55-8, 522-66-7)
6 alternate names
3 suppliers
91-48-5
(91-48-5, 3368-16-9)
6 alternate names
3 suppliers
vincamine
CAS Directory
