Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C20H26N2O3 · 2HCl
CAS Number:
Molecular Weight:
415.35
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.77
SMILES string
O[C@@]1(CC[C@@H](N)[C@]2([H])OC3=C4O)[C@]52C3=C(C=C4)C[C@H]1N(CC6CC6)CC5
InChI
1S/C20H26N2O3/c21-13-5-6-20(24)15-9-12-3-4-14(23)17-16(12)19(20,18(13)25-17)7-8-22(15)10-11-1-2-11/h3-4,11,13,15,18,23-24H,1-2,5-10,21H2/t13-,15-,18+,19+,20-/m1/s1
InChI key
SPPAUICKSNQRNC-GNUVVZJLSA-N
assay
≥98% (HPLC)
form
powder
Quality Level
color
white to beige
solubility
H2O: 25 mg/mL, clear
storage temp.
2-8°C
Biochem/physiol Actions
β-naltrexamine is obtained from naltrexone.
β-Naltrexamine is a potent opioid antagonist.
β-Naltrexamine is a potent orally available, long lasting opioid antagonist.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Morgan Le Naour et al.
Journal of medicinal chemistry, 55(2), 670-677 (2011-12-06)
Using the selective mu-kappa agonist, N-naphthoyl-β-naltrexamine 1, as the prototype ligand, a series of closely related naphthalene analogues were synthesized to study the chemical space around the naphthalene moiety in an effort to evaluate how receptor selectivity is affected by
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service