1,2,3,4,6,7,8,9-octahydrophenazine

AlkaPlorer ID: AK046492

Synonym: 'SMR000528198', 'MLS000737867'

IUPAC Name: 1,2,3,4,6,7,8,9-octahydrophenazine

Structure

SMILES: C1CCC2=NC3=C(CCCC3)N=C2C1

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InChI: InChI=1S/C12H16N2/c1-2-6-10-9(5-1)13-11-7-3-4-8-12(11)14-10/h1-8H2

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InChIKey: JYYRTWNCBVRKMN-UHFFFAOYSA-N

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Source

Species Genus Family Order Class Phylum Kingdom Domain
Idesia polycarpa Idesia Salicaceae Malpighiales Magnoliopsida Streptophyta Viridiplantae Eukaryota

Properties Information

Molecule Weight: 188.274

TPSA: 25.78

MolLogP: 2.2342000000000004

Number of H-Donors: 0

Number of H-Acceptors: 2

RingCount: 3

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Acinetobacter baumannii Acinetobacter baumannii Inhibition -4.6 % 10.6019/CHEMBL4296182
Candida albicans Candida albicans Inhibition 1.61 % 10.6019/CHEMBL4296182
Cryptococcus neoformans Cryptococcus neoformans Inhibition -2.79 % 10.6019/CHEMBL4296182
Escherichia coli Escherichia coli Inhibition 11.61 % 10.6019/CHEMBL4296182
Homo sapiens DNA-(apurinic or apyrimidinic site) lyase Potency 2511.9 nM None
Klebsiella pneumoniae Klebsiella pneumoniae Inhibition 13.7 % 10.6019/CHEMBL4296182
Macaca fascicularis T-complex protein 1 subunit beta Potency 12589.3 nM None
Plasmodium falciparum Plasmodium falciparum Potency 13115.4 nM None
Pseudomonas aeruginosa Pseudomonas aeruginosa Inhibition 19.99 % 10.6019/CHEMBL4296182
Staphylococcus aureus Staphylococcus aureus Inhibition 13.53 % 10.6019/CHEMBL4296182

Metabolism Information