Isradipine

CAS No. 75695-93-1

Isradipine( PN 200-110 )

Catalog No. M15878 CAS No. 75695-93-1

Isradipine is a potent and selective L-type voltage-gated calcium channel blocker, used to treat high blood pressure.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 30 In Stock
10MG 49 In Stock
25MG 88 In Stock
50MG 146 In Stock
100MG 243 In Stock
500MG 601 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Isradipine
  • Note
    Research use only, not for human use.
  • Brief Description
    Isradipine is a potent and selective L-type voltage-gated calcium channel blocker, used to treat high blood pressure.
  • Description
    Isradipine is a potent and selective L-type voltage-gated calcium channel blocker, used to treat high blood pressure.(In Vitro):Isradipine has much higher (>40 fold) affinity for Cav1.3 channels as well as good brain bioavailability. Isradipine has nearly equal potency at Cav1.2 and Cav1.3 channels.(In Vivo):Isradipine (0.1~3 mg/kg; p.o.) makes sodium excretion increase in a dose-dependent manner.Isradipine pre-treatment reduces 6-hydroxydopamine induced neurotoxicity at the striatal level. Protective effect of isradipine at the striatal level is dose-dependent as shown from 6 mice. Isradipine pre-treatment increases the number of surviving SNc DA cells after 6-hydroxydopamine induced degeneration. Isradipine is capable of protecting striatal dopaminergic terminals and SNc dopaminergic cell bodies against a slow, progressive insult created by intrastriatal injection of 6-hydroxydopamine.
  • In Vitro
    Isradipine has much higher (>40 fold) affinity for Cav1.3 channels as well as good brain bioavailability. Isradipine has nearly equal potency at Cav1.2 and Cav1.3 channels.
  • In Vivo
    Isradipine (0.1~3 mg/kg; p.o.) makes sodium excretion increase in a dose-dependent manner.Isradipine pre-treatment reduces 6-hydroxydopamine induced neurotoxicity at the striatal level. Protective effect of isradipine at the striatal level is dose-dependent as shown from 6 mice. Isradipine pre-treatment increases the number of surviving SNc DA cells after 6-hydroxydopamine induced degeneration. Isradipine is capable of protecting striatal dopaminergic terminals and SNc dopaminergic cell bodies against a slow, progressive insult created by intrastriatal injection of 6-hydroxydopamine. Animal Model:Rats Dosage:0.1~3 mg/kg Administration:P.o.Result:Sodium excretion increased in a dose-dependent manner. ?
  • Synonyms
    PN 200-110
  • Pathway
    GPCR/G Protein
  • Target
    Calcium Channel
  • Recptor
    Calcium Channel
  • Research Area
    Cardiovascular Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    75695-93-1
  • Formula Weight
    371.39
  • Molecular Formula
    C19H21N3O5
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 74 mg/mL warmed (199.25 mM); DMSO: 74 mg/mL (199.25 mM)
  • SMILES
    CC1=C(C(OC)=O)C(C2=CC=CC3=NON=C32)C(C(OC(C)C)=O)=C(C)N1
  • Chemical Name
    3-isopropyl 5-methyl 4-(benzo[c][1,2,5]oxadiazol-4-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Ilijic E, et al. Neurobiol Dis. 2011 Aug;43(2):364-7
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