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Antiviral API
- Arenavirus
- Cytomegalovirus (CMV)
- Dengue virus
- Endogenous Metabolite
- Enterovirus (EV)
- Epstein-Barr virus (EBV)
- Filovirus
- Flavivirus
- HCV Protease
- Hepatitis B Virus (HBV)
- Hepatitis C Virus (HCV)
- Herpes simplex Virus (HSV)
- HIF/HIF Prolyl-Hydroxylase
- HIV Integrase
- HIV Protease
- Human immunodeficiency Virus (HIV)
- Human papillomavirus (HPV)
- Influenza Virus
- Nipah virus
- Orthopoxvirus
- Others
- Rabies virus (RABV)
- Respiratory syncytial Virus (RSV)
- Reverse Transcriptases (RTs)
- SARS-CoV
- Tobacco mosaic virus (TMV)
- Vesicular stomatitis virus (VSV)
- Virus Protease
- West Nile virus
- Antiviral intermediates
1-Adamantanamine-[d15]
Category | Influenza Virus |
CAS | 33830-10-3 |
Description | 1-Adamantanamine-[d15] is a labelled form of Amantadine. Amantadine can be used as an antiviral and an antiparkinsonian drug. It is an NMDA receptor antagonist. Amantadine is also a useful building block in organic synthesis, allowing the insertion of an adamantyl group. |
Product Information
Synonyms | (Adamantan-1-yl-d15)amine; 1-Adamant-d15-amine; 1-Adamantyl-d15-amine; 1-Amantadine-d15; 1-Aminoadamantane-d15; Adamantamine-d15; Adamantan-d15-amine; Adamantyl-d15amine; Amantadine-d15; NSC 341865-d15; Tricyclo[3.3.1.13,7]decane-d15-1-amine |
IUPAC Name | 2,2,3,4,4,5,6,6,7,8,8,9,9,10,10-pentadecadeuterioadamantan-1-amine |
Molecular Weight | 166.34 |
Molecular Formula | C10H2D15N |
Canonical SMILES | C1C2CC3CC1CC(C2)(C3)N |
InChI | InChI=1S/C10H17N/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9H,1-6,11H2/i1D2,2D2,3D2,4D2,5D2,6D2,7D,8D,9D |
InChIKey | DKNWSYNQZKUICI-BXSQCBKHSA-N |
Melting Point | >160°C (dec.) |
Purity | 95% |
Solubility | Soluble in DMSO (Slightly), Methanol (Slightly, Sonicated) |
Appearance | White to Light Beige Solid |
Storage | Store at -20°C |
Complexity | 144 |
Exact Mass | 187.112778 |
In Vitro | Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and Metabolic profiles of drugs. |
Target | Influenza Virus |
XLogP3-AA | 2.4 |