7-AMINO-3-BETA-D-RIBOFURANOSYL-1H-PYRAZOLO[4,3-D]PYRIMIDINE MONOHYDRATE
7-AMINO-3-BETA-D-RIBOFURANOSYL-1H-PYRAZOLO[4,3-D]PYRIMIDINE MONOHYDRATE Basic information
- Product Name:
- 7-AMINO-3-BETA-D-RIBOFURANOSYL-1H-PYRAZOLO[4,3-D]PYRIMIDINE MONOHYDRATE
- Synonyms:
-
- 3-d)pyrimidin-3-yl)-1,4-anhydro-1-c-(7-amino-1h-pyrazolo((s)-d-ribito
- 3-d)pyrimidine,7-amino-3-beta-d-ribofuranosyl-1h-pyrazolo(
- 7-amino-3-beta-d-ribofuranosyl-1h-pyrazolo(4,3-d)pyrimidine
- formycin
- 8-AZA-9-DEAZAADENOSINE MONOHYDRATE
- 7-AMINO-3-BETA-D-RIBOFURANOSYL-1H-PYRAZOLO[4,3-D]PYRIMIDINE MONOHYDRATE
- FORMYCIN MONOHYDRATE
- FORMYCIN A MONOHYDRATE
- CAS:
- 6742-12-7
- MF:
- C10H13N5O4
- MW:
- 267.25
- Mol File:
- 6742-12-7.mol
7-AMINO-3-BETA-D-RIBOFURANOSYL-1H-PYRAZOLO[4,3-D]PYRIMIDINE MONOHYDRATE Chemical Properties
- Melting point:
- 141-144 °C (decomp)
- Boiling point:
- 709.5±60.0 °C(Predicted)
- Density
- 1.771±0.06 g/cm3(Predicted)
- storage temp.
- −20°C
- solubility
- DMSO: soluble1mg/mL
- form
- powder
- pka
- 8.37±0.50(Predicted)
- color
- white to off-white
- BRN
- 624229
7-AMINO-3-BETA-D-RIBOFURANOSYL-1H-PYRAZOLO[4,3-D]PYRIMIDINE MONOHYDRATE Usage And Synthesis
Description
Formycin (Formycin A) is isolated from Nocardia interforma and from Streptomyces lavendulae , . The antibiotic is effective against Xanthomonas oryzae and Pellicularia filamentosa. Its activity against Yoshida rat sarcoma cell is enhanced by coformycin. Formycin B inhibits Xanthomonas oryzae and interferes with multiplication of influenza A virus in the cells of chick chorioallantoic membrane . Oxoformycin B shows no activity against Xanthomonas oryzae .
Uses
Formycin A (NSC 102811), a purine nucleoside antibiotic, is a potent human immunodeficiency virus type 1 (HIV-1) inhibitor with an EC50 of 10 μM. Formycin A shows antitumor and antiviral activities[1][2].
Definition
ChEBI: Formycin A is a formycin. It has a role as an antineoplastic agent.
IC 50
HIV-1: 10 μM (EC50)
References
[1] Dapp MJ , et al. Discovery of novel ribonucleoside analogs with activity against human immunodeficiency virus type 1.J Virol. 2014 Jan;88(1):354-63. DOI:10.1128/JVI.02444-13
[2] Zhang M, et al. Comparative Investigation into Formycin A and Pyrazofurin A Biosynthesis Reveals Branch Pathways for the Construction of C-Nucleoside Scaffolds. Appl Environ Microbiol. 2020 Jan 7;86(2). DOI:10.1128/AEM.01971-19
7-AMINO-3-BETA-D-RIBOFURANOSYL-1H-PYRAZOLO[4,3-D]PYRIMIDINE MONOHYDRATESupplier
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