Weight | 98.08 g/mol |
---|---|
Formula | C4H3FN2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2-fluoropyrimidine (31575-35-6)
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- 2-Fluoropyrimidine RNA-based Aptamers to the 165-Amino Acid Form of Vascular Endothelial Growth Factor (VEGF165) INHIBITION OF RECEPTOR BINDING AND VEGF-INDUCED VASCULAR PERMEABILITY THROUGH INTERACTIONS REQUIRING THE EXON 7-ENCODED DOMAIN (Journal of Biological Chemistry, 1998)
- Acquisition of Human Concentrative Nucleoside Transporter 2 (hCNT2) Activity by Gene Transfer Confers Sensitivity to Fluoropyrimidine Nucleosides in Drug-Resistant Leukemia Cells (Molecular Pharmacology, 2001)
- Safety and efficacy of bevacizumab (Bev) when added to oxaliplatin/fluoropyrimidine (O/F) regimens as first-line treatment of metastatic colorectal cancer (mCRC): TREE 1 & 2 Studies (Journal of Clinical Oncology, 2005)
- Novel cytostatic 2',3'-dideoxy-3'-fluoropyrimidine-nucleosides (1969)
- Intratumoral COX-2 Gene Expression Is a Predictive Factor for Colorectal Cancer Response to Fluoropyrimidine-Based Chemotherapy (Clinical Cancer Research, 2005)
- Comparative anti-herpesvirus activities of 9-(1,3-dihydroxy-2-propoxymethyl)guanine, acyclovir, and two 2'-fluoropyrimidine nucleosides. (Antiviral Research, 1985)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN=C(N=C1)F
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InChIKeyWAVYAFBQOXCGSZ-UHFFFAOYSA-N
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Similar Compounds
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(675-12-7)
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(17180-93-7)
1 alternate name
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(38353-06-9)
1 alternate name
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2,5-Diaminopyrimidine
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1 alternate name
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(32779-38-7)
1 alternate name
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(32779-36-5)
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(35231-56-2)
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1 alternate name
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(7752-82-1)
1 alternate name
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(5428-89-7)
1 alternate name
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(2434-56-2, 77709-02-5)
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39889-94-6
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(156-81-0)
1 alternate name
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1 alternate name
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(108-79-2)
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(19808-30-1)
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(38275-56-8)
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(1004-38-2)
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(675-14-9)
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1 alternate name
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(693-98-1)
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