ARANIDIPINE
- Product Name
- ARANIDIPINE
- CAS No.
- 86780-90-7
- Chemical Name
- ARANIDIPINE
- Synonyms
- Sapresta;MPC-1304;ARANIDIPINE;Asanidipine;Aranidipine MPC1304;ARANIDIPINE USP/EP/BP;Aranidipine, 10 mM in DMSO;ARANIDIPINE MPC1304;MPC-1304;MPC 1304;Calcium Channel,inhibit,MPC 1304,Inhibitor,MPC-1304,Aranidipine,Ca channels,Ca2+ channels;3-Methyl 5-(2-oxopropyl) 2,6-diMethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
- CBNumber
- CB4386708
- Molecular Formula
- C19H20N2O7
- Formula Weight
- 388.37
- MOL File
- 86780-90-7.mol
ARANIDIPINE Property
- Melting point:
- 155°
- Boiling point:
- 530.0±50.0 °C(Predicted)
- Density
- 1.284±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- DMSO : 125 mg/mL (321.86 mM)
- form
- Solid
- pka
- 2.56±0.70(Predicted)
- color
- Light yellow to yellow
Safety
- Toxicity
- LD50 in male, female mice, rats (mg/kg): 143, 193, 1982, 1459 orally; LD50 in male, female mice (mg/kg): 7.3, 9.1 i.p. (Nakano)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- CS-7341
- Product name
- Aranidipine
- Purity
- 99.33%
- Packaging
- 5mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- CS-7341
- Product name
- Aranidipine
- Purity
- 99.33%
- Packaging
- 10mg
- Price
- $105
- Updated
- 2021/12/16
- Product number
- CS-7341
- Product name
- Aranidipine
- Purity
- 99.33%
- Packaging
- 50mg
- Price
- $315
- Updated
- 2021/12/16
- Product number
- CS-7341
- Product name
- Aranidipine
- Purity
- 99.33%
- Packaging
- 100mg
- Price
- $535
- Updated
- 2021/12/16
- Product number
- orb573449
- Product name
- Aranidipine (MPC1304)
- Purity
- >98%
- Packaging
- 100mg
- Price
- $986
- Updated
- 2021/12/16
ARANIDIPINE Chemical Properties,Usage,Production
Description
Aranidipine was launched in Japan as an antihypertensive agent. Its pharmacological effects are similar to other dihydropyridine derivatives, e.g., nefidipine, however, it is more potent and longer lasting. This is partially due to the fact that its initial metabolite (ketone reduction) is just as effective as the parent compound. Aranidipine exerts its activity by blocking Ca+2 entry during depolarization via L-type voltagegated Ca channels. This causes decreased levels of intracellular Ca which leads to enhanced relaxation of smooth and cardiac muscle. It is a selective α2-adrenoreceptor antagonist which inhibits vasoconstrictive responses. As a dihydropyridine derivative, it can be synthesized via a modified Hantsch synthesis. While sold as a racemate, the (S)-enantiomer is 150 times more active than the (R)- antipode.
Chemical Properties
Yellow prismatic crystals from ethyl acetate-hexane, melting point 155°C. Acute toxicity LD50 male and female mice, male and female rats (mg/kg): 143, 193, 1982, 1459 orally. Acute toxicity LD50 male and female mice (mg/kg): 7.3, 9.1 intraperitoneal injection.
Originator
Maruko Seiyaku (Japan)
Definition
ChEBI: Aranidipine is an organic molecular entity.
Manufacturing Process
100.0 mg of 50% sodium hydride was added to a mixture of 20.0 g of 2,2-
ethylenedioxypropanol and 100 ml of benzene, and 20.0 g of diketene was
added dropwise to the mixture while refluxing the mixture. After refluxing the
mixture for 2 h, the solvent was distilled off and the resulting residue was
distilled under reduced pressure to obtain 21.5 g (70% yield) of 2,2-
ethylenedioxypropyl acetoacetate as a colorless oil, boiling point of 90°C (6
mm Hg).
Ammonia gas was passed through a mixture of 19.0 g of 2,2-
ethylenedioxypropyl acetoacetate and 100 ml of methanol for 2.5 h under icecooling
while stirring. The solvent was then distilled off and the residue was
distilled under reduced pressure to obtain 16.0 g (84% yield) of 2,2-
ethylenedioxypropyl 3-aminocrotonate as a pale yellow oil, boiling point of
120°C (5 mm Hg).
A mixture of methyl 2'-nitrobenzylidene acetoacetate, 2,2-ethylenedioxypropyl
3-aminocrotonate and ethanol was refluxed for 10 h. The resulting reaction
solution was allowed to stand overnight, and the precipitated crystals were
collected by filtration and recrystallized from ethanol to obtain methyl 2,2-
ethylenedioxypropyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-
dicarboxylate.
Methyl 2,2-ethylenedioxypropyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-
dihydropyridine-3,5-dicarboxylate was refluxed in an ethanol solution
containing 10% hydrochloric acid for 6 h. The solvent was then distilled off
and the residue was crystallized from diethyl ether to give methyl 2-oxopropyl
2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate as
yellow prisms, melting point 155°C (recrystallized from a mixture of ethyl
acetate and hexane).
brand name
Bec/Sapresta
Therapeutic Function
Antihypertensive
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View Lastest Price from ARANIDIPINE manufacturers
- Product
- Aranidipine 86780-90-7
- Price
- US $0.00-0.00/KG
- Min. Order
- 1KG
- Purity
- 99.0%
- Supply Ability
- 500 MT
- Release date
- 2020-05-11