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N7634

Nifedipine

Name: Nifedipine
Brand: SIGMA

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

Synonyme(s) :

1,4-Dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5-pyridinedicarboxylic acid dimethyl ester

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A propos de cet article

Formule empirique (notation de Hill) :

C₁₇H₁₈N₂O₆

Numéro CAS:

21829-25-4

Poids moléculaire :

346.33

NACRES:

NA.77

PubChem Substance ID:

24277855

UNSPSC Code:

12352200

EC Number:

244-598-3

MDL number:

MFCD00057326

Assay:

≥98% (HPLC)

Form:

powder

Quality level:

200

Service technique

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Propriétés

Nom du produit

Nifedipine, ≥98% (HPLC), powder

Quality Level

200

assay

≥98% (HPLC)

form

powder

color

yellow

solubility

DMSO: soluble, ethanol: soluble

originator

Bayer

storage temp.

2-8°C

SMILES string

COC(=O)C1=C(C)NC(C)=C(C1c2ccccc2[N+]([O-])=O)C(=O)OC

InChI

1S/C17H18N2O6/c1-9-13(16(20)24-3)15(14(10(2)18-9)17(21)25-4)11-7-5-6-8-12(11)19(22)23/h5-8,15,18H,1-4H3

InChI key

HYIMSNHJOBLJNT-UHFFFAOYSA-N

Gene Information

human ... ADORA2A(135), ADORA3(140), CACNA1C(775), CACNA1D(776), CACNA1F(778), CACNA1S(779), CACNA2D1(781), CYP1A2(1544), KCNH1(3756), TTR(7276)
mouse ... Cacna1c(12288)
rat ... Adora1(29290), Adora2a(25369), Cacna1c(24239), Cacna1d(29716), Kcnj1(24521), Kcnn4(65206), Tbxas1(24886)

Description

Application

Nifedipine has been used:

to evaluate its effect on myenteric neuronal calcium current through R-type calcium channel in guinea pig small intestine
to evaluate the neuroprotective effect of L-type calcium channel blockers in cholinergic and dopaminergic neurons
to identify the effect of co-administration of nifedipine (anti-hypertensive drug) along with hypoglycemic drug on human umbilical vein cells (HUVECs)

Biochem/physiol Actions

Nifedipine is a L-type Ca²⁺ channel blocker; and induces apoptosis in human glioblastoma cells. Nifedipine has neuroprotection activity and protects substantia nigra. Nifedipine has antioxidant potential. Nifedipine downregulates inflammatory cytokines like macrophage inflammatory protein-2 (MIP-2), tumor necrosis factor-α (TNF-α). Nifedipine has antihypertensive properties. Nifedipine inhibits extracellular region of adenosine A2a receptor (ADORA2A) gene.

Features and Benefits

This compound is a featured product for ADME Tox and Cyclic Nucleotide research. Discover more featured ADME Tox and Cyclic Nucleotide products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

This compound is featured on the Calcium Channels and Cyclic Nucleotide-Gated (CNG) and Hyperpolarization Activated Cyclic Nucleotide-Gated (HCN) Channels pages 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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pictograms

GHS07

signalword

Warning

hcodes

H302

pcodes

P264 - P270 - P301 + P312 + P330 - P501

Hazard Classifications

Acute Tox. 4 Oral

Classe de stockage

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Contenu apparenté

Product Information Sheet - N7634

Product Information Sheet

Cell-type-specific interrogation of CeA Drd2 neurons to identify targets for pharmacological modulation of fear extinction

McCullough KM, et al.

Translational Psychiatry, 8(1), 164-164 (2018)

Combination therapy of nifedipine and sulphonyl ureas exhibits a mutual antagonistic effect on the endothelial cell dysfunction induced by hyperglycemia linked to vascular disease

Wang LP, et al.

Cellular Physiology and Biochemistry, 38(6), 2337-2347 (2016)

R-type calcium channels in myenteric neurons of guinea pig small intestine

Bian X, et al.

American Journal of Physiology: Gastrointestinal and Liver Physiology, 287(1), G134-G142 (2004)

Afficher tous les articles scientifiques apparentés