Isovincamine

HCID 5668

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

IsovincamineDTXSID90274475RefChem:1087856DTXCID6022595418374-18-0Vinca14-EpivincamineMLS00073821216-EpivincamineNSC91998methyl 15-ethyl-17-hydroxy-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene-17-carboxylateMethyl 14-hydroxy-14,15-dihydroeburnamenine-14-carboxylate
Show more names
MinorineVincaminVraapPervalEquipurMonorinNovicetPervone
Methyl (3alpha,14alpha,16alpha)-14,15-dihydro-14-hydroxyeburnamenine-14-carboxylateVincachronVincasaunierVinkametrinDecincanDevinkanMinorinVincapan

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

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

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

Chemistry & industry

Applications · 3 items

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 · 1 item

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.

Suppliers100 total

北京华美互利生物化工010-56205725 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
成都普瑞法科技开发有限公司+86-028-82633397 18982077548 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
北京安司莫森技术有限公司010-82954736 13391601435 · [email protected]
Additional notes · 1 item

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

3 records

Compound notes

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