Nimodipine-d7
For Laboratory Research Only. Not for Clinical or Personal Use.
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Nimodipine-d7
Description :
Nimodipine-d7 is the deuterium labeled Nimodipine. Nimodipine (BAY-e 9736) is an orally active, well-tolerated and light-sensitive dihydropyridine calcium antagonist. Nimodipine can be used for the research of cerebrovascular disorders[1].Product Name Alternative :
BAY-e 9736-d7UNSPSC :
12352005Hazard Statement :
H302, H315, H319, H335Target :
Autophagy; Calcium Channel; Isotope-Labeled CompoundsType :
Isotope-Labeled CompoundsRelated Pathways :
Autophagy; Membrane Transporter/Ion Channel; Neuronal Signaling; OthersField of Research :
Cardiovascular Disease; CancerPurity :
99.35Solubility :
DMSO : 100 mg/mL (ultrasonic; warming)Smiles :
O=C(C1=C(C)NC(C)=C(C(OC(C([2H])([2H])[2H])([2H])C([2H])([2H])[2H])=O)C1C2=CC=CC([N+]([O-])=O)=C2)OCCOCMolecular Formula :
C21H19D7N2O7Molecular Weight :
425.48Precautions :
H302, H315, H319, H335References & Citations :
[1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53 (2) :211-216. |[2]Langley, M.S., et al. Nimodipine. Drugs 37, 669–699 (1989) .|[3] Marbacher S, et al. Prevention of delayed cerebral vasospasm by continuous intrathecal infusion of glyceroltrinitrate and nimodipine in the rabbit model in vivo. Intensive Care Med. 2008;34 (5) :932-938.|[4]Honn KV, et al. Inhibition of tumor cell-platelet interactions and tumor metastasis by the calcium channel blocker, nimodipine. Clin Exp Metastasis. 1984;2 (1) :61-72.Shipping Conditions :
Blue IceStorage Conditions :
-20°C, 3 years (Powder)Scientific Category :
Isotope-Labeled CompoundsClinical Information :
No Development ReportedCAS Number :
[1246815-36-0]

