Emtricitabine 5-fluorouracil analog

Product Name Emtricitabine 5-fluorouracil analog
Alternate Names Emtricitabine Impurities, Impurities of Emtricitabine
CAT No. CS-O-16331
CAS No. 145986-11-4
Category Impurities
Stock IN-Stock
Mol. Wt. 248.23 g/mol
Mol. For. C₈H₉FN₂O₄S
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Emtricitabine
Therapeutic Antiretroviral / Anti-HIV
Canonical Smiles C1C(OC(S1)CO)N2C=C(C(=O)NC2=O)F
InchIKey KOGYOPLNKQJQFM-NTSWFWBYSA-N
Inchl InChI=1S/C8H9FN2O4S/c9-4-1-11(8(14)10-7(4)13)5-3-16-6(2-12)15-5/h1,5-6,12H,2-3H2,(H,10,13,14)/t5-,6+/m0/s1
IUPAC 5-fluoro-1-[(2R,5S)-2-(hydroxymethyl)-1,3-oxathiolan-5-yl]pyrimidine-2,4-dione
Controlled No
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Emtricitabine 5-fluorouracil analog is a synthetic nucleoside analogue that is primarily used to treat HIV (human immunodeficiency virus) infections. Its chemical structure closely resembles that of 5-fluorouracil, a chemotherapy drug used to treat various types of cancer. Emtricitabine works by inhibiting the reverse transcriptase enzyme, which is responsible for the replication of HIV in the body. By inhibiting this enzyme, emtricitabine prevents the virus from replicating and spreading throughout the body, ultimately reducing the viral load and slowing the progression of the disease. Emtricitabine is typically administered orally in the form of a tablet or capsule. It is often used in combination with other antiretroviral drugs to create a highly active antiretroviral therapy (HAART) regimen. The drug is generally well-tolerated, with few serious side effects reported. However, some individuals may experience mild side effects such as nausea, headache, and diarrhea. In terms of chemical information, emtricitabine is a cytidine analogue that is structurally similar to zalcitabine and lamivudine. It has a molecular weight of 247.25 g/mol and a chemical formula of C8H10FN3O3S. Emtricitabine is a white to off-white crystalline powder that is soluble in water and ethanol. Overall, emtricitabine 5-fluorouracil analog is a highly effective antiretroviral drug that has revolutionized the treatment of HIV infections. Its ability to inhibit the replication of the virus has made it a cornerstone of HIV therapy, and its relative safety and tolerability make it a popular choice among healthcare providers.

Related Compounds

Emtricitabine Menthyl Ester(2S,5R Isomer) | Emtricitabine+Tenofovir FT1 | N-Acetyl O-Benzoyl 5-Epi Emtricitabine | Emtricitabine lactose adduct | Emtricitabine Disulfide | ent-Emtricitabine | Emtricitabine Impurity 6 | Emtricitabine Dimer Impurity | Emtricitabine diastereomer(mixture) | Emtricitabine F6 Impurity | Emtricitabine Glycosamine | Emtricitabine+Tenofovir FT5 | Emtricitabine Racemic Mixture | Desamino Emtricitabine | Emtricitabine (R)-sulphoxide | conjugate Impurity of Tenofovir+Emtricitabine | Emtricitabine+Tenofovir FT4 | Emtricitabine FTU Impurity | Emtricitabine methyl ester | Emtricitabine+Tenofovir FT6 | Cis-cyclo-Emtricitabine | Emtricitabine 6-Disulfide | Emtricitabine Tenofovir Monosoproxil Dimer | Emtricitabine Impurity 8 | Trans-cyclo-Emtricitabine | Emtricitabine+Tenofovir FT2 | Emtricitabine Impurity | Emtricitabine+Tenofovir FT3 | Emtricitabine Impurity 9 | Emtricitabine+Des-Phenol Tenofovir Alfenamide Mixed Dimer | Emtricitabine Impurity 11 | Cyclic Diastereomeric Impurity Isomer-2 | Emtricitabine Tenofovir Disoproxil Dimer | Emtricitabine Diastereomer | Emtricitabine dioxolane | Emtricitabine (S)-sulphoxide |

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