Basic information
- CAS
1617-90-9- Standard SMILES
CCC12CCCN3CCc4c(n(c5ccccc45)C(O)(C(=O)OC)C1)C32- InChIKey
RXPRRQLKFXBCSJ-UHFFFAOYSA-N- Molecular formula
- C21H26N2O3
- Average molar mass
- 354.4 g/mol
- Monoisotopic mass
- 354.1943427
Names & identifiers
- Preferred name
- Isovincamine
- IUPAC
- methyl 15-ethyl-17-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene-17-carboxylate
- English name
- Vincamine
- Molecular formula
- C21H26N2O3
- Molecular weight
- 354.44
Names & synonyms
Show more names
Database identifiers
- CAS
1617-90-9、18374-18-0、6835-99-0- PubChem CID
- 5668
- ChEMBL
CHEMBL1604925- ChEBI
CHEBI:107202
Properties
Computed structural properties
- XLogP
- 2.9
- Topological polar surface area
- 54.7 Ų
- Hydrogen bond donors
- 1
- Hydrogen bond acceptors
- 4
- Rotatable bonds
- 3
- Heavy atoms
- 26
- Formal charge
- 0
- Complexity
- 598
Physicochemical properties
- Melting point
- 232 °C · 232 °C (dec.)(lit.)
- alpha
- 42.8 · 42.8 º (c=1 in pyridine)
- Boiling point
- 487.66 °C · 487.66°C (rough estimate)
- Density
- 1.164 · 1.1640 (rough estimate)
- refractive index
- 1.65 · 1.6500 (estimate)
- storage temp.
- 2 · Keep in dark place,Inert atmosphere,2-8°C
- solubility
- Chloroform (Slightly), DMSO (Slightly)
- form
- Solid
- pka
- 12.13 · 12.13±0.40(Predicted)
- color
- White to Off-White
- optical activity
- 23 · [α]23/D +42.8°, c = 1 in pyridine
- Merck
- 14 · 14,9983
- Stability
- Hygroscopic
- Major Application
- food and beverages
- InChI
- 1S/C21H26N2O3/c1-3-20-10-6-11-22-12-9-15-14-7-4-5-8-16(14)23(17(15)18(20)22)21(25,13-20)19(24)26-2/h4-5,7-8,18,25H,3,6,9-13H2,1-2H3/t18-,20+,21+/m1/s1
- InChIKey
- RXPRRQLKFXBCSJ-GIVPXCGWSA-N
- SMILES
- CC[C@@]12CCCN3CCc4c(C13)n(c5ccccc45)[C@](O)(C2)C(=O)OC
- LogP
- 3.1 · 3.100 (est)
- EWG's Food Scores
- 1 · 1
- FDA UNII
- 996 XVD0JHT · 996XVD0JHT
- ATC code
- 4 AX07 · C04AX07
- NIST Chemistry Reference
- Vincamine(1617-90-9)
- UNSPSC Code
- 12352200 · 12352200
- NACRES
- 24 · NA.24
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 302 · H302
- Precautionary statements
- 264 · P264-P270-P301+P312-P501
- Hazard Codes
- Xn
- Risk Statements
- 22 · 22
- Safety Statements
- 36 · 36-26
- WGK Germany
- 3 · 3
- RTECS
- 8575000 · YY8575000
- HS Code
- 29399990 · 29399990
- Storage Class
- 11 · 11 - Combustible Solids
- Hazard Classifications
- 4 Oral · Acute Tox. 4 Oral
- Hazardous Substances Data
- 1617 · 1617-90-9(Hazardous Substances Data)
- Toxicity
- 50 in · LD50 in mice (mg/kg): 75 i.v.; >1000 s.c. (Szporny, Szász); 1000 orally (Szabo, Nagy)
Safety & regulation
Safety data
- wgk
- 3
- rtecs
- YY8575000
- hs_code
- 29399990
- Toxicity
- LD50 in mice (mg/kg): 75 i.v.; >1000 s.c. (Szporny, Szász); 1000 orally (Szabo, Nagy)
- risk_code
- 22
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xn
- safety_code
- 36-26
- Storage Class
- 11 - Combustible Solids
- Hazard statements
- H302
- Hazard Classifications
- Acute Tox. 4 Oral
- Precautionary statements
- P264-P270-P301+P312-P501
- Hazardous Substances Data
- 1617-90-9(Hazardous Substances Data)
Chemistry & industry
Applications
DescriptionVincamine is an alkaloid extracted from the leaves of the Vinca minor and is a related synthetic ethyl ester of vincaminic acid. It has spasmolytic effects similar to reserpine and can potentially improve blood flow in the brain.
UsesVincamine is often used as a nootropic agent to combat the effects of aging, or in conjunction with other nootropics (such as piracetam) for a variety of purposes. Vincamine is a peripheral vasodilator that increases blood flow to the brain.
General DescriptionVincamine is a monoterpenoid indole alkaloid found in the leaves of Vinca minor L., belonging to the Apocynaceae family.
Preparation methods
PreparationA method for preparing Vincamine, the method comprising the following steps: 1) Preparation of taponin: Taponin hydrochloride is freed in petroleum ether using concentrated ammonia, and then an acid salt solution is added to remove the remaining ammonia. After the reaction is completed, the aqueous layer is extracted with petroleum ether, the organic phases are combined, the organic phases are dried with a drying agent, filtered, and the filtrate is distilled under reduced pressure to obtain taponin; 2) Preparation of Vincamine: Taponin obtained in step (1) is dissolved in an organic solvent, Pd/C is added under stirring, and the reaction is carried out under a hydrogen atmosphere and normal pressure at a certain temperature. The reaction endpoint is monitored by TLC, filtered, and the filtrate is distilled under reduced pressure to obtain Vincamine; 3) Preparation of monoperoxymaleic acid: Maleic anhydride is dissolved in N,N-dimethylformamide, 30% hydrogen peroxide is added dropwise, and the reaction is carried out after the addition is complete. After the reaction is completed, the temperature is lowered, and the solution is diluted with cold methanol for later use; 4) Preparation of Vincamine: The Vincamine obtained in step (2) was dissolved in methanol, cooled, and a certain amount of monoperoxymaleic acid obtained in step (3) was added dropwise. After the oxidation reaction was carried out for a period of time, a certain amount of monoperoxymaleic acid was added dropwise. After the addition was completed, the oxidation reaction was continued for a period of time. After the reaction was completed, a reducing agent solution was added dropwise until the starch KI test paper no longer changed color. The temperature was raised to carry out the rearrangement reaction. After the reaction was completed, the temperature was lowered to 20-30℃, and a certain amount of water and concentrated ammonia were added to adjust the pH to a certain range. The temperature was lowered to crystallize, filtered, and the filter cake was washed with methanol and water. Then, it was pulped with water at a certain temperature, filtered, and the filter cake was dried under reduced pressure to obtain Vincamine.
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers100 total
Additional notes
DefinitionChEBI: Vincamine is a vinca alkaloid, an alkaloid ester, an organic heteropentacyclic compound, a methyl ester and a hemiaminal. It has a role as an antihypertensive agent, a vasodilator agent and a metabolite. It is functionally related to an eburnamenine.
Related reactions
Compound notes
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