Weight | 279.189 g/mol |
---|---|
Formula | C8H14N3O6P |
Hydrogen Acceptors | 7 |
Hydrogen Donors | 4 |
Aromatic Rings | 1 |
Rotatable Bonds | 6 |
Cidofovir (113852-37-2)
Score:
#145 in Microbiology
,
#1500 in Biology
,
#1761 in Chemistry
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- The Antiviral Nucleotide Analogs Cidofovir and Adefovir Are Novel Substrates for Human and Rat Renal Organic Anion Transporter 1 (Molecular Pharmacology, 1999)
- Intravenous Cidofovir for Peripheral Cytomegalovirus Retinitis in Patients with AIDS: A Randomized, Controlled Trial (Annals of Internal Medicine, 1997)
- Cytotoxicity of Antiviral Nucleotides Adefovir and Cidofovir Is Induced by the Expression of Human Renal Organic Anion Transporter 1 (Journal of The American Society of Nephrology, 2000)
- Clinical Potential of the Acyclic Nucleoside Phosphonates Cidofovir, Adefovir, and Tenofovir in Treatment of DNA Virus and Retrovirus Infections (Clinical Microbiology Reviews, 2003)
- Clinical Pharmacokinetics of the Antiviral Nucleotide Analogues Cidofovir and Adefovir (Clinical Pharmacokinectics, 1999)
- Treatment of Severe Laryngeal Papillomatosis With Intralesional Injections of Cidofovir ((S)-1-(3-Hydroxy-2-Phosphonylmethoxypropyl) Cytosine) (Journal of Medical Virology, 1998)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN(C(=O)N=C1N)CC(CO)OCP(=O)(O)O
-
InChIKeyVWFCHDSQECPREK-UHFFFAOYSA-N
- Pubchem - Cidofovir
- Wikipedia - cidofovir anhydrous
Cidofovir (brand name Vistide) is an injectable antiviral medication primarily used as a treatment for cytomegalovirus (CMV) retinitis (an infection of the retina of the eye) in people with AIDS. Cidofovir was approved for medical use in 1996.
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