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MW 346.3 Da, Purity >99%. L-type Ca2+ channel blocker. Potent, long-acting vasodilator. Also shown to inhibit vascular inflammation.

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Images

Chemical Structure - Nifedipine, L-type Ca2+ channel blocker (AB120135), expandable thumbnail
  • Functional Studies - Nifedipine, L-type Ca2+ channel blocker (AB120135), expandable thumbnail

Publications

Key facts

CAS number
21829-25-4
Purity
> 99%
Form
Solid
Molecular weight
346.3 Da
Molecular formula
C17H18N2O6
PubChem identifier
4485
Nature
Synthetic

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MW 346.3 Da, Purity >99%. L-type Ca2+ channel blocker. Potent, long-acting vasodilator. Also shown to inhibit vascular inflammation.

Key facts

Purity
> 99%
PubChem identifier
4485
Solubility

Soluble in DMSO to 100 mM.

Biochemical name
Nifedipine
Biological description

L-type Ca2+ channel blocker. Potent, long-acting vasodilator. Also shown to inhibit vascular inflammation.

Canonical SMILES
CC1=C(C(C(=C(N1)C)C(=O)OC)C2=CC=CC=C2[N+](=O)[O-])C(=O)OC
InChI
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
InChIKey
HYIMSNHJOBLJNT-UHFFFAOYSA-N
IUPAC name
dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

Storage

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
Store under desiccating conditions, The product can be stored for up to 12 months

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2 product images

  • Chemical Structure - Nifedipine, L-type Ca2+ channel blocker (ab120135), expandable thumbnail

    Chemical Structure - Nifedipine, L-type Ca2+ channel blocker (ab120135)

    2D chemical structure image of ab120135, Nifedipine, L-type Ca2+ channel blocker

  • Functional Studies - Nifedipine, L-type Ca2+ channel blocker (ab120135), expandable thumbnail

    Functional Studies - Nifedipine, L-type Ca2+ channel blocker (ab120135)

    ab2770 staining aryl hydrocarbon receptor in MDA-MB-231 cells treated with nifedipine (ab120135), by ICC/IF. Increase in aryl hydrocarbon receptor expression correlates with increased concentration of nifedipine, as described in literature.
    The cells were incubated at 37°C for 6h in media containing different concentrations of ab120135 (nifedipine) in DMSO, fixed with 100% methanol for 5 minutes at -20°C and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with ab2770 (1/100 dilution) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight 488 goat anti-mouse polyclonal antibody (Goat Anti-Mouse IgG H&L (DyLight® 488) preadsorbed ab96879) at 1/250 dilution was used as the secondary antibody. Nuclei were counterstained with DAPI and are shown in blue.

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