Pyocyanin

Details

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Internal ID c1be105c-57d8-443c-9bf8-3fbc4380281e
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name 5-methylphenazin-1-one
SMILES (Canonical) CN1C2=CC=CC=C2N=C3C1=CC=CC3=O
SMILES (Isomeric) CN1C2=CC=CC=C2N=C3C1=CC=CC3=O
InChI InChI=1S/C13H10N2O/c1-15-10-6-3-2-5-9(10)14-13-11(15)7-4-8-12(13)16/h2-8H,1H3
InChI Key YNCMLFHHXWETLD-UHFFFAOYSA-N
Popularity 743 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10N2O
Molecular Weight 210.23 g/mol
Exact Mass 210.079312947 g/mol
Topological Polar Surface Area (TPSA) 32.70 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.04
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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PYOCYANINE
85-66-5
Sanazin
Sanasin
Pyrocyanine
5-methylphenazin-1-one
5-Methyl-1(5H)-phenazinone
5-methylphenazin-1(5H)-one
5-methylphenazin-5-ium-1-olate
1(5H)-Phenazinone, 5-methyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Pyocyanin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9893 98.93%
Caco-2 + 0.8940 89.40%
Blood Brain Barrier + 0.9317 93.17%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8609 86.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9624 96.24%
OATP1B3 inhibitior + 0.9611 96.11%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.8987 89.87%
P-glycoprotein substrate - 0.9432 94.32%
CYP3A4 substrate - 0.5134 51.34%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.8730 87.30%
CYP3A4 inhibition - 0.7457 74.57%
CYP2C9 inhibition - 0.9677 96.77%
CYP2C19 inhibition - 0.9274 92.74%
CYP2D6 inhibition - 0.9214 92.14%
CYP1A2 inhibition + 0.8672 86.72%
CYP2C8 inhibition - 0.9007 90.07%
CYP inhibitory promiscuity - 0.5202 52.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5584 55.84%
Eye corrosion - 0.9795 97.95%
Eye irritation + 0.7252 72.52%
Skin irritation - 0.6997 69.97%
Skin corrosion - 0.9335 93.35%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5968 59.68%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8634 86.34%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6168 61.68%
Acute Oral Toxicity (c) III 0.6970 69.70%
Estrogen receptor binding + 0.6706 67.06%
Androgen receptor binding - 0.5473 54.73%
Thyroid receptor binding + 0.6508 65.08%
Glucocorticoid receptor binding + 0.8495 84.95%
Aromatase binding + 0.7716 77.16%
PPAR gamma + 0.5913 59.13%
Honey bee toxicity - 0.9595 95.95%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity - 0.9225 92.25%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.49% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.38% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.19% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.15% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.32% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.22% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.18% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.60% 96.09%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.05% 96.67%
CHEMBL4072 P07858 Cathepsin B 84.85% 93.67%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 84.23% 92.67%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.15% 93.65%
CHEMBL1781 P11387 DNA topoisomerase I 83.85% 97.00%
CHEMBL1907 P15144 Aminopeptidase N 83.74% 93.31%
CHEMBL255 P29275 Adenosine A2b receptor 82.53% 98.59%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.53% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.18% 82.69%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 80.86% 100.00%
CHEMBL4040 P28482 MAP kinase ERK2 80.51% 83.82%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 6817
LOTUS LTS0226836
wikiData Q410503