Date published: 2025-9-26

1-800-457-3801

SCBT Portrait Logo
Seach Input

7-Aminoflavone (CAS 15847-18-4)

0.0(0)
Write a reviewAsk a question

See product citations (1)

CAS Number:
15847-18-4
Purity:
97%
Molecular Weight:
237.25
Molecular Formula:
C15H11NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

7-Aminoflavone (7-AF) is a flavonoid compound derived from various plants. Studies have explored the inhibitory effects of 7-Aminoflavone on the growth of specific bacteria, fungi, and viruses. The precise mechanism of action behind 7-Aminoflavone′s biological activities is not yet fully elucidated. However, it is postulated that 7-Aminoflavone exerts its effects by modulating the activity of key enzymes and proteins involved in cellular growth regulation, apoptosis, and the expression of genes.


7-Aminoflavone (CAS 15847-18-4) References

  1. Cytotoxic properties of titanocenyl amides on breast cancer cell line mcf-7.  |  Gao, LM. and Meléndez, E. 2010. Met Based Drugs. 2010: 286298. PMID: 20454639
  2. Synthesis and biological activity assays of some new N1-(flavon-7-yl)amidrazone derivatives and related congeners.  |  Abu-Aisheh, MN., et al. 2012. Eur J Med Chem. 54: 65-74. PMID: 22677031
  3. Evaluation of the structure-activity relationship of flavonoids as antioxidants and toxicants of zebrafish larvae.  |  Chen, YH., et al. 2012. Food Chem. 134: 717-24. PMID: 23107683
  4. Triazine-based mesoporous covalent imine polymers as solid supports for copper-mediated Chan-Lam cross-coupling N-arylation reactions.  |  Puthiaraj, P. and Pitchumani, K. 2014. Chemistry. 20: 8761-70. PMID: 24938420
  5. Insect Antifeedant Potential of Xanthohumol, Isoxanthohumol, and Their Derivatives.  |  Stompor, M., et al. 2015. J Agric Food Chem. 63: 6749-56. PMID: 26176501
  6. Chromenone-conjugated magnetic iron oxide nanoparticles. Toward conveyable DNA binders.  |  Yousuf, S., et al. 2015. Colloids Surf B Biointerfaces. 135: 448-457. PMID: 26280819
  7. Stepwise conversion of flavonoids by engineered dioxygenases and dehydrogenase: Characterization of novel biotransformation products.  |  Overwin, H., et al. 2015. Enzyme Microb Technol. 81: 63-71. PMID: 26453473
  8. The synthesis, lipophilicity and cytotoxic effects of new ruthenium(II) arene complexes with chromone derivatives.  |  Pastuszko, A., et al. 2016. J Inorg Biochem. 159: 133-41. PMID: 26986980
  9. Synthesis of fused pyrroles containing 4-hydroxycoumarins by regioselective metal-free multicomponent reactions.  |  Mishra, R., et al. 2018. Org Biomol Chem. 16: 3289-3302. PMID: 29667668
  10. Synthesis and biological evaluation of novel flavone/triazole/benzimidazole hybrids and flavone/isoxazole-annulated heterocycles as antiproliferative and antimycobacterial agents.  |  Rao, YJ., et al. 2018. Mol Divers. 22: 803-814. PMID: 29869169
  11. Biotransformations of Flavones and an Isoflavone (Daidzein) in Cultures of Entomopathogenic Filamentous Fungi.  |  Dymarska, M., et al. 2018. Molecules. 23: PMID: 29874813
  12. Synthesis and cytotoxic activities of organometallic Ru(II) diamine complexes.  |  Kavukcu, SB., et al. 2020. Bioorg Chem. 99: 103793. PMID: 32278205
  13. Shortwave infrared polymethine fluorophores matched to excitation lasers enable non-invasive, multicolour in vivo imaging in real time.  |  Cosco, ED., et al. 2020. Nat Chem. 12: 1123-1130. PMID: 33077925
  14. The Roles of HIF-1α in Radiosensitivity and Radiation-Induced Bystander Effects Under Hypoxia.  |  Zhang, J., et al. 2021. Front Cell Dev Biol. 9: 637454. PMID: 33869184
  15. Cytotoxic effect, generation of reactive oxygen/nitrogen species and electrochemical properties of Cu(ii) complexes in comparison to half-sandwich complexes of Ru(ii) with aminochromone derivatives.  |  Mucha, P., et al. 2019. RSC Adv. 9: 31943-31952. PMID: 35530753

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

7-Aminoflavone, 1 g

sc-227111
1 g
$41.00