A database of FDA approved therapeutic peptides and proteins
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1059 details |
| Primary information | |
|---|---|
| ThPP ID | Th1010 |
| Therapeutic Peptide/Protein Name | Interferon alfa-n1 |
| Sequence | CDLPQTHSLGSRRTLMLLAQMRKISLFSCLKDRHDFGFPQEEFGNQFQKA view full sequnce in fasta |
| Functional Classification | Ib |
| Molecular Weight | 19241.1 |
| Chemical Formula | C860H1353N227O255S9 |
| Isoelectric Point | 5.99 |
| Hydrophobicity | -0.336 |
| Melting Point (℃) | 61 |
| Half Life | 1.2 hours (mammalian reticulocytes, in vitro) |
| Description | Purified, natural and glycosylated human interferon alpha proteins of 166 residues. |
| Indication/Disease | Used to treat venereal or genital warts caused by the Human Papiloma Virus. |
| Pharmacodynamics | Upregulates the expression of MHC I proteins, allowing increased presentation of peptides derived from viral antigens. This enhances the activation of CD8+ T cells that are the precursors for cytotoxic T lymphocytes and makes the macrophage a better target for CTL-mediated killing. Interferon alpha also induce the synthesis of several key antiviral mediators, including 2-5-oligoadenylate synthetase (2'-5' A synthetase) and protein kinase R. |
| Mechanism of Action | Interferon alpha binds to type I interferon receptors namely IFNAR1 and IFNAR2c which, upon dimerization, activate two Jak (Janus kinase) tyrosine kinases (Jak1 and Tyk2). These transphosphorylate themselves and phosphorylate the receptors. The phosphorylated INFAR receptors then bind to Stat1 and Stat2 (signal transducers and activators of transcription)which dimerize and activate multiple (~100) immunomodulatory and antiviral proteins. Interferon alpha binds less stably to type I interferon receptors than interferon beta. |
| Toxicity | N.A. |
| Metabolism | N.A. |
| Absorption | N.A. |
| Volume of Distribution | N.A. |
| Clearance | N.A. |
| Categories | Antiviral Agents |
| Patents Number | N.A. |
| Date of Issue | N.A. |
| Date of Expiry | N.A. |
| Drug Interaction | Interferon increases the effect and toxicity of theophylline |
| Target | Interferon alpha/beta receptor 1,Interferon alpha/beta receptor 2 |
| Information of corresponding available drug in the market | |
| Brand Name | Wellferon |
| Company | GlaxoSmithKline |
| Brand Discription | Wellferon is a purified blend of natural human alpha interferons which are obtained from human lympho-blastoid cells following induction with Sendai virus. Wellferon resembles human leukocyte interferon as it is a mixture of natural alpha subtypes but dif |
| Prescribed for | Used for the treatment of patients with hairy cell leukemia, juvenile laryngeal papillomatosis, condylomata acuminata, chronic hepatitis B and chronic hepatitis C infections. |
| Chemical Name | N.A. |
| Formulation | Each vial of clear, colorless solution contains interferon alpha-n1 (lns) [purified human lymphoblastoid interferon] 3, 5 or 10 mega units. 1 mega unit (Mu)=1´10International Units (IU) of lymphoblastoid interferon. Formulated in 1 mL tris-glycine buffere |
| Physcial Appearnce | Solution |
| Route of Administration | Injection |
| Recommended Dosage | N.A. |
| Contraindication | Hypersensitivity |
| Side Effects | Most side/adverse effects, except the flu-like syndrome, are dose-related . They are usually mild to moderate at systemic doses less than 10 million Units per day }; hematologic and hepatic toxicities tend to be more frequent with doses above 10 million |
| Useful Link | http://www.drugs.com/mmx/wellferon.html |
| PubMed ID | 9537453, 9305672, 1861694, 2016626, 3046638, 3170795, 3278186, 3488481, 3016426 |
| 3-D Structure | Th1010 (View) or (Download) |