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N149

Nimodipine

≥98% (HPLC), L-type Ca2+ channel antagonist, powder

Synonym(s):

1,4-Dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylic acid 2-methoxyethyl 1-methylethyl ester, Isopropyl 2-methoxyethyl 1,4-dihydro-2,6-dimethyl-4-(m-nitrophenyl)-3,5-pyridinedicarboxylate

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Size/SKUAvailabilityPrice
100 mg
Please contact Customer Service for Availability
2 660,00 CZK
500 mg
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10 600,00 CZK

About This Item

Empirical Formula (Hill Notation):
C21H26N2O7
CAS Number:
Molecular Weight:
418.44
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
266-127-0
MDL number:
Assay:
≥98% (HPLC)
Form:
powder

2 660,00 CZK


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Product Name

Nimodipine,

assay

≥98% (HPLC)

Quality Segment

form

powder

color

off-white to yellow

solubility

methanol: 62.5 mg/mL, 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: insoluble, H2O: insoluble

originator

Bayer

SMILES string

COCCOC(=O)C1=C(C)NC(C)=C(C1c2cccc(c2)[N+]([O-])=O)C(=O)OC(C)C

InChI

1S/C21H26N2O7/c1-12(2)30-21(25)18-14(4)22-13(3)17(20(24)29-10-9-28-5)19(18)15-7-6-8-16(11-15)23(26)27/h6-8,11-12,19,22H,9-10H2,1-5H3

InChI key

UIAGMCDKSXEBJQ-UHFFFAOYSA-N

Application

Nimodipine has been used:
  • as a L-type calcium channel (LTCC) inhibitor, to evaluate its neuroprotective activity in the vibrosections
  • as a standard, in the enantioseparation of chiral drugs by high performance liquid chromatography (HPLC)
  • in the pharmacological studies for the measurement of spine voltage escape

Biochem/physiol Actions

Nimodipine is a potent L-type Ca2+ channel antagonist.
Nimodipine enhances the survival of dopaminergic substantia nigra neurons.

Features and Benefits

This compound is featured on the Calcium Channels page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by Bayer. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

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This Item
1463858482200N0850000
description

-

description

United States Pharmacopeia (USP) Reference Standard

description

An L-type Ca2+ channel blocker.

description

European Pharmacopoeia (EP) Reference Standard

form

powder

form

-

form

solid

form

-

assay

≥98% (HPLC)

assay

-

assay

>98% (HPLC)

assay

-

Quality Level

200

Quality Level

-

Quality Level

100

Quality Level

-

solubility

45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: insoluble, methanol: 62.5 mg/mL, H2O: insoluble

solubility

-

solubility

DMSO: 25 mg/mL, methanol: soluble

solubility

-

color

off-white to yellow

color

-

color

yellow

color

-

Gene Information

human ... ADORA3(140), CACNA1C(775), CACNA1D(776), CACNA1F(778), CACNA1S(779), CACNG1(786), NR3C2(4306)
rat ... Adora1(29290), Adora2a(25369)

Gene Information

human ... CACNA1C(775), CACNA1D(776), CACNA1F(778), CACNA1S(779), NR3C2(4306)

Gene Information

-

Gene Information

human ... CACNA1C(775), CACNA1D(776), CACNA1F(778), CACNA1S(779), NR3C2(4306)


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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Codes

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

PPE (personal protective equipment)

dust mask type N95 (US), Eyeshields, Gloves



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