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1g Pack Size. Group: Biochemicals, Building Blocks. Formula: C9H11FN2O5. CAS No. 50-91-9. Prepack ID 27134875-1g. Molecular Weight 246.19. See USA prepack pricing.
5-Fluoro-2'-deoxyuridine, 99+%
5-Fluoro-2'-deoxyuridine, 99+%. Group: Biochemicals. Alternative Names: 5-Fluoro-2'-deoxy-D-uridine; Floxuridine; 2'-Deoxy-5-fluorouridine; 1-(2-Deoxy--D-ribofuranosyl)-5-fluorouracil; NSC-27640; FUDR. Grades: Reagent Grade. CAS No. 50-91-9. Pack Sizes: 250mg, 1g, 5g, 25g. Molecular Formula: C9H11FN2O5, Molecular Weight: 246.19. US Biological Life Sciences.
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Floxuridine
Floxuridine (5-Fluorouracil 2'-deoxyriboside) is a pyrimidine analog and known as an oncology antimetabolite. Floxuridine inhibits Poly(ADP-Ribose) polymerase and induces DNA damage by activating the ATM and ATR checkpoint signaling pathways in vitro. Floxuridine is a extreamly potent inhibitor for S. aureus infection and induces cell apoptosis [1] [2]. Floxuridine has antiviral effects against HSV and CMV [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 5-Fluorouracil 2'-deoxyriboside. CAS No. 50-91-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 200 mg; 500 mg. Product ID: HY-B0097.
Floxuridine
Floxuridine (5-Fluorouracil 2'-deoxyriboside) is a pyrimidine analog and known as an oncology antimetabolite. Floxuridine inhibits Poly(ADP-Ribose) polymerase and induces DNA damage by activating the ATM and ATR checkpoint signaling pathways in vitro. Floxuridine is a extreamly potent inhibitor for S. aureus infection and induces cell apoptosis. Floxuridine has antiviral effects against HSV and CMV. Group: Inhibitors. Alternative Names: 1-beta-d-2'-deoxyribofuranosyl-5-flurouracil;1beta-D-2-Deoxyribofuranosyl-5-fluorouracil;2'-deoxy-5-fluoro-uridin;5-fluor-1-(beta-2'-deoxyribofuranosyl)pyrimidin-2,4(1h,3h)-dion;5-Fluor-1-(beta-2-deoxyribofuranosyl)pyrimidin-2,4(1H,3H)-dion;5-Fluoro-2-deoxyiridine;5-Fluorouracil 2-deoxyriboside;5-Fluorouracil deoxyriboside. CAS No. 50-91-9. Molecular formula: C9H11FN2O5. Mole weight: 246.19. Purity: 0.9995. Catalog: ACM50919.
Floxuridine
Floxuridine is an antineoplastic antimetabolite, used in the treatment of colon carcinoma and colorectal cancer that has metastasized to the liver. Synonyms: Deoxyfluorouridine; FDUR; NSC 27640; NSC27640; NSC-27640; 2'-Deoxy-5-fluorouridine; 1-(2-Deoxy-β-D-ribofuranosyl)-5-fluorouracil; 5-Fluoro-2'-deoxy-uridine; 5-Fluorodeoxyuridine; 5-Fluorouracil 2'-Deoxyriboside; FdUrd. Grades: ≥95%. CAS No. 50-91-9. Molecular formula: C9H11FN2O5. Mole weight: 246.19.
An intermediate for the preparation of (3R,5S)-Fluvastatin. Group: Biochemicals. Alternative Names: (4R,6S)-6-[(1E)-2-[3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]ethenyl]-2,2-dimethyl-1,3-dioxane-4-acetic Acid 1,1-Dimethylethyl Ester. Grades: Highly Purified. CAS No. 500731-91-9. Pack Sizes: 5mg. US Biological Life Sciences.
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(S)-Albuterol Hydrochloride
The S-enantiomer of Albuterol. A β2-adrenoceptor agonist. Bronchodilator; tocolytic. Group: Biochemicals. Alternative Names: (α 1S) -α 1-[[ (1, 1-Dimethylethyl) amino]methyl]-4-hydroxy-1, 3-benzenedimethanol Hydrochloride; (+)-Salbutamol Hydrochloride; (S)-Salbutamol Hydrochloride. Grades: Highly Purified. CAS No. 50293-91-9. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
(S)-Salbutamol Hydrochloride
(S)-Salbutamol Hydrochloride. Uses: For analytical and research use. Group: Impurity standards. CAS No. 50293-91-9. Molecular Formula: C13H22ClNO3. Mole Weight: 275.77. Catalog: APB50293919.
(S)- Salbutamol ((S)-Albuterol)
(S)-Salbutamol.Salbutamol is a short-acting, selective beta2-adrenergic receptor agonist used in the treatment of asthma and COPD. It is 29 times more selective for beta2 receptors than beta1 receptors giving it higher specificity for pulmonary beta receptors versus beta1-adrenergic receptors located in the heart. Synonyms: (α1S)-α1-[[(1,1-Dimethylethyl)amino]methyl]-4-hydroxy-1,3-benzenedimethanol Hydrochloride; (+)-Salbutamol Hydrochloride; (S)-Salbutamol Hydrochloride. Grades: > 95%. CAS No. 50293-91-9. Molecular formula: C13H21NO3 HCl. Mole weight: 275.78.
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