ARANIDIPINE
- CAS No.
- 86780-90-7
- Chemical Name:
- ARANIDIPINE
- Synonyms
- Sapresta;MPC-1304;ARANIDIPINE;Asanidipine;Aranidipine MPC1304;ARANIDIPINE USP/EP/BP;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;2,6-Dimethyl-4-(2-nitrophenyl)-1,4-dihydro-3,5-pyridinedicarboxylic acid methyl 2-oxopropyl ester
- CBNumber:
- CB4386708
- Molecular Formula:
- C19H20N2O7
- Molecular Weight:
- 388.37
- MDL Number:
- MFCD00865813
- MOL File:
- 86780-90-7.mol
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 |
FDA UNII | 4Y7UR6X2PO |
SAFETY
Risk and Safety Statements
Symbol(GHS) | GHS07 |
---|---|
Signal word | Warning |
Hazard statements | H302+H312+H332 |
Precautionary statements | P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P501 |
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) |
ARANIDIPINE price
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
ChemScene | CS-7341 | Aranidipine 99.33% | 86780-90-7 | 5mg | $60 | 2021-12-16 | Buy |
ChemScene | CS-7341 | Aranidipine 99.33% | 86780-90-7 | 10mg | $105 | 2021-12-16 | Buy |
ChemScene | CS-7341 | Aranidipine 99.33% | 86780-90-7 | 50mg | $315 | 2021-12-16 | Buy |
ChemScene | CS-7341 | Aranidipine 99.33% | 86780-90-7 | 100mg | $535 | 2021-12-16 | Buy |
Biorbyt Ltd | orb573449 | Aranidipine (MPC1304) >98% | 86780-90-7 | 100mg | $986 | 2021-12-16 | Buy |
ARANIDIPINE Chemical Properties,Uses,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.
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
ARANIDIPINE Preparation Products And Raw materials
Supplier | Tel | Country | ProdList | Advantage | |
---|---|---|---|---|---|
ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 | ivan@atkchemical.com | China | 32836 | 60 |
Shaanxi Dideu Medichem Co. Ltd | +86-029-89586680 +86-18192503167 | 1026@dideu.com | China | 7730 | 58 |
Dayang Chem (Hangzhou) Co.,Ltd. | 571-88938639 +8617705817739 | info@dycnchem.com | China | 52861 | 58 |
InvivoChem | +1-708-310-1919 +1-13798911105 | sales@invivochem.cn | United States | 6393 | 58 |
TargetMol Chemicals Inc. | +1-781-999-5354 | support@targetmol.com | United States | 19973 | 58 |
PT CHEM GROUP LIMITED | peter68@ptchemgroup.com | China | 35426 | 58 | |
LGM Pharma | 1-(800)-881-8210 | inquiries@lgmpharma.com | United States | 2127 | 70 |
Hangzhou Yuhao Chemical Technology Co., Ltd | 0571-82693216 | info@yuhaochemical.com | China | 9394 | 52 |
Shanghai T&W Pharmaceutical Co., Ltd. | +86 21 61551611 | China | 9900 | 58 | |
MedChemexpress LLC | 021-58955995 | sales@medchemexpress.cn | United States | 4863 | 58 |
View Lastest Price from ARANIDIPINE manufacturers
Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
---|---|---|---|---|---|---|---|---|
2020-05-12 | Aranidipine
86780-90-7
|
US $0.00-0.00 / KG | 1KG | 99.0% | 500 MT | Shaanxi Dideu Medichem Co. Ltd |
- Aranidipine
86780-90-7
- US $0.00-0.00 / KG
- 99.0%
- Shaanxi Dideu Medichem Co. Ltd