2,6-Dimethylnaphthalene-d12
Based on 1 Customer Validation
2,6-Dimethylnaphthalene-d12 is the deuterated-labeled 2,6-Dimethylnaphthalene (HY-W017280). 2,6-Dimethylnaphthalene is a cytochrome P450 1A2 (CYP1A2) inhibitor, with an IC50 of 52 μM and a pIC50 of 4.28 against human targets. 2,6-Dimethylnaphthalene inhibits the 7-ethoxyresorufin O-dealkylation activity catalyzed by CYP1A2.
For research use only. We do not sell to patients.
- Purity: 98.85%
- CAS No.: 350820-12-1
- Formula: C12D12
- Molecular Weight:168.30
-
Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
Biological Activity
|
CYP1A2 52 μM (IC50) |
CYP1A2 4.28 μM (pIC50) |
1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Chemical Information
-
CAS No. 350820-12-1
-
Appearance Solid
-
Molecular Weight 168.30
-
Formula C12D12
-
Color White to off-white
-
SMILES
[2H]C([2H])([2H])C(C([2H])=C1[2H])=C([2H])C(C([2H])=C2[2H])=C1C([2H])=C2C([2H])([2H])[2H]
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Purity & Documentation
-
Data Sheet (273 KB)
-
SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
-
Handling Instructions (2659 KB)
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
- 2,6-Dimethylnaphthalene-d12
- 350820-12-1
- Isotope-Labeled Compounds
- Cytochrome P450
- 2,6-naphthalene dicarboxylic acid
- Pd-zeolite catalysts
- Pd-HBeta
- recombinant human CYP1A2
- 7-ethoxyresorufin O-dealkylation
- PEN
- NH4F and SrO co-modified HZSM-5 catalyst
- CYP1A2
- cytochrome P450 1A2
- poly(ethylene naphthalate)
- Inhibitor
- inhibitor
- inhibit