Cyclopropyldiaminopurine Abacavir

Chemical Name Cyclopropyldiaminopurine Abacavir
Alternate Names Abacavir Impurities, Impurities of Abacavir
CAT No. CS-P-00494
CAS Registry# 120503-69-7
Category Impurities
Stock IN-Stock
Mol. Wt. 190.21 g/mol
Mol. For. C₈H₁₀N₆
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Abacavir
Therapeutic Antiretroviral / Anti-HIV
Canonical Smiles C1CC1NC2=NC(=NC3=C2NC=N3)N
InchIKey IYWUSKBMXQERLH-UHFFFAOYSA-N
Inchl InChI=1S/C8H10N6/c9-8-13-6-5(10-3-11-6)7(14-8)12-4-1-2-4/h3-4H,1-2H2,(H4,9,10,11,12,13,14)
IUPAC 6-N-cyclopropyl-7H-purine-2,6-diamine
Controlled No
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Cyclopropyldiaminopurine Abacavir, commonly known as Abacavir, is an antiviral medication used to treat HIV/AIDS. It belongs to the class of nucleoside reverse transcriptase inhibitors (NRTIs) and works by blocking the reverse transcriptase enzyme, which is essential for the virus to replicate. Abacavir is typically prescribed as part of a combination therapy to treat HIV-1 infection in adults and children over the age of three months. It is available in tablet form and is taken orally, usually twice a day. The chemical formula for Abacavir is C14H18N6O, and it has a molecular weight of 286.33 g/mol. The drug is rapidly absorbed after oral administration and has a bioavailability of approximately 83%. It is predominantly metabolized by the liver and excreted in the urine. Abacavir can cause some side effects, including hypersensitivity reactions, which can be life-threatening. Patients taking Abacavir are advised to carry a warning card with them at all times and to seek immediate medical attention if they experience symptoms such as fever, rash, nausea, or vomiting. In conclusion, Abacavir is a powerful antiviral medication that is used in the treatment of HIV/AIDS. It has a specific chemical structure and mechanism of action that make it effective against the virus. However, patients must be closely monitored for potential side effects and hypersensitivity reactions.

Related Compounds

Abacavir 5-(2,3,4-Tri-O-isobytyryl)-ß-D-glucuronic Acid Methyl Ester | Clorabacavir racemic | Abacavir impurity N-Oxide | Abacavir Lopinavir Methylene Conjugation | Abacavir Impurity 4 | Abacavir Impurity B | Abacavir Nitroso Impurity | O-fomyl Abacavir | Chloro Abacavir | Abacavir EP Impurity D | Abacavir EP Impurity F | Abacavir EP Impurity A Sulfate Salt | ent-abacavir | trans-Abacavir Dihydrochloride |

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