| Weight | 225.204 g/mol |
|---|---|
| Formula | C9H11N3O4 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
ANCITABINE (31698-14-3, 10212-25-6)
Cyclocytidine · Anhydro-Ara-C · U 33,624A
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- Cyclocytidine-induced release of nerve growth factor from mouse submandibular glands enhances regeneration of sympathetic fibers in adult mice (Brain Research, 1985)
- Stimulation of secretion of epidermal growth factor and amylase by cyclocytidine (Cell and Tissue Research, 1978)
- Studies on the Vilsmeier-Haack reaction. IV. Convenient synthesis of 2,2'-anhydro-1- -D-arabinofuranosylcytosine (2,2'-cyclocytidine) and its derivatives. (Journal of Organic Chemistry, 1972)
- Drug Stability in Liposomal Suspensions: Hydrolysis of Indomethacin, Cyclocytidine, and p-Nitrophenyl Acetate (Journal of Pharmaceutical Sciences, 1982)
- 2,2'-O-cyclocytidine, an antitumor cytidine analog resistant to cytidine deaminase. (GANN Japanese Journal of Cancer Research, 1971)
- Molecular structure of 2,2-anhydro-1--D-arabinofuranosyl cytosine hydrochloride (cyclo ARA-C): A highly rigid nucleoside (Biochemical and Biophysical Research Communications, 1973)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Cyclocytidine
- Anhydro-Ara-C
- U 33,624A
- NSC 145668
- NSC-145668
- NSC-145,668
- NSC 145,668
- U-33,624A
- U-33624A
- U33,624A
- Cyclo-C
- Cyclo C
- CycloC
- U 33624A
- U33624A
- NSC145,668
- NSC145668
-
SMILESC1=CN2C3C(C(C(O3)CO)O)OC2=NC1=N
-
InChIKeyBBDAGFIXKZCXAH-UHFFFAOYSA-N
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