10212-30-3
- Name: 4(1H)-Pyrimidinone,2-amino-1-b-D-arabinofuranosyl-
- Chemical Name: 2-amino-1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-4-one
- CAS Number: 10212-30-3
- Molecular Formula: C9H13N3O5
- Molecular Weight: 243.22
- Catalog: Signaling Pathways Cell Cycle/DNA Damage Nucleoside Antimetabolite/Analog
- Create Date: 2016-08-08 21:27:16
- Modify Date: 2024-01-10 14:09:40
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2-Amino-1-β-D-arabinofuranosyl-4(1H)-pyrimidinone is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
| Name | 2-amino-1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-4-one |
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| Description | 2-Amino-1-β-D-arabinofuranosyl-4(1H)-pyrimidinone is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1]. |
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| References |
| Density | 1.89g/cm3 |
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| Boiling Point | 545.7ºC at 760mmHg |
| Molecular Formula | C9H13N3O5 |
| Molecular Weight | 243.22 |
| Flash Point | 283.8ºC |
| Exact Mass | 243.08600 |
| PSA | 131.82000 |
| Vapour Pressure | 3.5E-14mmHg at 25°C |
| Index of Refraction | 1.756 |
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10212-30-3 |
| Literature: Ozaki, Hiroaki; Nakajima, Kiyohiro; Tatsui, Kaoru; Izumi, Chieko; Kuwahara, Masayasu; Sawai, Hiroaki Bioorganic and Medicinal Chemistry Letters, 2003 , vol. 13, # 15 p. 2441 - 2443 |
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10212-30-3 |
| Literature: Brown et al. Journal of the Chemical Society, 1956 , p. 2388,2392 Journal of the Chemical Society, 1958 , p. 3028,3032 |
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10212-30-3 |
| Literature: Brown et al. Journal of the Chemical Society, 1958 , p. 3028,3033 Full Text Show Details Brown et al. Journal of the Chemical Society, 1956 , p. 2388,2392 Journal of the Chemical Society, 1958 , p. 3028,3032 |
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10212-30-3 |
| Literature: Brown et al. Journal of the Chemical Society, 1956 , p. 2388,2392 Journal of the Chemical Society, 1958 , p. 3028,3032 |
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10212-30-3 |
| Literature: Brown et al. Journal of the Chemical Society, 1956 , p. 2388,2392 Journal of the Chemical Society, 1958 , p. 3028,3032 |
|
~%
10212-30-3 |
| Literature: Brown et al. Journal of the Chemical Society, 1956 , p. 2388,2392 Journal of the Chemical Society, 1958 , p. 3028,3032 |
|
~%
10212-30-3 |
| Literature: Brown et al. Journal of the Chemical Society, 1956 , p. 2388,2392 Journal of the Chemical Society, 1958 , p. 3028,3032 |
|
~%
10212-30-3 |
| Literature: Brown et al. Journal of the Chemical Society, 1958 , p. 3028,3033 |
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10212-30-3 |
| Literature: Brown et al. Journal of the Chemical Society, 1958 , p. 3028,3033 |
| Precursor 7 | |
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| DownStream 1 | |