66-71-7

o-Phenanthroline Chemical Structure
66-71-7

Chemical Structure

o-Phenanthroline

Synonym(s): 1,10-Phenanthroline

  • CAS No.: 66-71-7
  • Formula:C12H8N2
  • Molecular Weight:180.21

IUPAC Name: 1,10-phenanthroline

InChIKey: DGEZNRSVGBDHLK-UHFFFAOYSA-N

SMILES: C12=C(N=CC=C3)C3=CC=C1C=CC=N2

Biological Activity: o-Phenanthroline (1,10-Phenanthroline), a metal chelator, prevents the induction of chromosomal aberrations in streptozotocin-treated cells. o-Phenanthroline (1,10-Phenanthroline) forms a red chelate with Fe2+ that absorbs maximally at 510 nm. o-Phenanthroline (1,10-Phenanthroline) is also a MMP inhibitor[1][2].

Cat. No. Product Name Purity Description Pricing
HY-W004544
o-Phenanthroline 99.95% o-Phenanthroline (1,10-Phenanthroline), a metal chelator, prevents the induction of chromosomal aberrations in streptozotocin-treated cells. o-Phenanthroline (1,10-Phenanthroline) forms a red chelate with Fe2+ that absorbs maximally at 510 nm. o-Phenanthroline (1,10-Phenanthroline) is also a MMP inhibitor.
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HY-W004544S
o-Phenanthroline-d8 o-Phenanthroline-d8 is the deuterium labeled o-Phenanthroline. o-Phenanthroline (1,10-Phenanthroline), a metal chelator, prevents the induction of chromosomal aberrations in streptozotocin-treated cells. o-Phenanthroline (1,10-Phenanthroline) forms a red chelate with Fe2+ that absorbs maximally at 510 nm. o-Phenanthroline (1,10-Phenanthroline) is also a MMP inhibitor.
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HY-184810
1,10-Phenanthrolin-2-amine 1,10-Phenanthrolin-2-amine is an antimycoplasmal agent whose anti-mycoplasmal activity depends on the presence of non-toxic copper. 1,10-Phenanthrolin-2-amine forms a complex with copper, thereby transporting copper into mycoplasma cells, where copper inhibits energy-supplying metabolic processes. 1,10-Phenanthrolin-2-amine can be used in studies of Mycoplasma gallisepticum infection.
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HY-59024
δ-Carboline δ-Carboline is a nitrogen-containing heterocyclic compound, and its derivatives all exhibit anti-cancer and antibacterial activities.
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HY-B1005
8-Hydroxyquinoline 99.95% 8-Hydroxyquinoline (8-Quinolinol) is a lipophilic metal chelator that can be used as a fungicide .8-Hydroxyquinoline shows the MIC range of 27.56-55.11 μM (4-8 μg/mL) against the clinical isolates of Neisseria gonorrhoeae. 8-Hydroxyquinoline can bind to copper form complexes and transport copper into cells. 8-Hydroxyquinoline increases in the number of micronucleated polychromatic erythrocytes and can also make hair depigmented in mice.
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HY-W002277
1,8-Naphthyridine 1,8-Naphthyridine is a heterocyclic compound with antibacterial and antitumor activities. 1,8-Naphthyridine is promising for research of antibacterial agents and cancers.
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HY-W004567
5-Chloro-1,10-phenanthroline 5-Chloro-1,10-phenanthroline is a metal-organic framework (MOF).
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HY-W004769
Benzo[h]quinoline 99.86% Benzo[h]quinolone is a widespread environmental pollutant. Benzo[h]quinolone is mutagenic. Benzo(h)quinoline derivatives can serve as G-quadruplex binding agents.
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HY-W007317
8-Aminoquinoline 99.96% 8-Aminoquinoline is a chelating ligand and intermediate. 8-Aminoquinoline assists metal-catalyzed direct C (sp2)-H and unactivated C (sp3)-H bond functionalization, copper-mediated C-H/C-H coupling, as well as copper/silver-catalyzed aryl C (sp2)-H amination reactions. 8-Aminoquinoline forms cationic Pt (II) complexes with anti-tumor activity. 8-Aminoquinoline is used in research related to latent malaria, glioblastoma, pancreatic adenocarcinoma, adenocarcinoma and biphasic mesothelioma.
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HY-W142745
Phenanthridine Phenanthridine is an aldehyde oxidase 1 (AOX1) substrate, with oxidation by hAOX1 yielding phenanthridone when molecular oxygen, ferricyanide, or dichlorophenolindophenol serves as electron acceptor.
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HY-Y1841
o-Phenanthroline monohydrate 99.95% o-Phenanthroline (1,10-Phenanthroline) monohydrate, a metal chelator, prevents the induction of chromosomal aberrations in streptozotocin-treated cells. o-Phenanthroline monohydrate forms a red chelate with Fe2+ that absorbs maximally at 510 nm. o-Phenanthroline (1,10-Phenanthroline) monohydrate is also a MMP inhibitor.
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References