(-)-Streptophenazine N

Details

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Internal ID f81d01ab-c120-4224-9755-61e87678c56d
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name (2R)-2-[(S)-hydroxy-(6-methoxycarbonylphenazin-1-yl)methyl]-7-methyloctanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H28N2O5/c1-14(2)8-4-5-9-17(23(28)29)22(27)15-10-6-12-18-20(15)25-19-13-7-11-16(21(19)26-18)24(30)31-3/h6-7,10-14,17,22,27H,4-5,8-9H2,1-3H3,(H,28,29)/t17-,22-/m1/s1
InChI Key FNSRQTYQIYLNST-VGOFRKELSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H28N2O5
Molecular Weight 424.50 g/mol
Exact Mass 424.19982200 g/mol
Topological Polar Surface Area (TPSA) 110.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.52
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (-)-Streptophenazine N

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8185 81.85%
Caco-2 - 0.8012 80.12%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7243 72.43%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.9425 94.25%
OATP1B3 inhibitior + 0.9125 91.25%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9252 92.52%
P-glycoprotein inhibitior + 0.6754 67.54%
P-glycoprotein substrate - 0.5127 51.27%
CYP3A4 substrate + 0.5818 58.18%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.8925 89.25%
CYP3A4 inhibition - 0.8777 87.77%
CYP2C9 inhibition - 0.7804 78.04%
CYP2C19 inhibition - 0.7739 77.39%
CYP2D6 inhibition - 0.8950 89.50%
CYP1A2 inhibition - 0.6546 65.46%
CYP2C8 inhibition + 0.4846 48.46%
CYP inhibitory promiscuity - 0.7745 77.45%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6751 67.51%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9476 94.76%
Skin irritation - 0.8153 81.53%
Skin corrosion - 0.9501 95.01%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5663 56.63%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8883 88.83%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6406 64.06%
Acute Oral Toxicity (c) III 0.6711 67.11%
Estrogen receptor binding + 0.6494 64.94%
Androgen receptor binding + 0.6756 67.56%
Thyroid receptor binding - 0.5349 53.49%
Glucocorticoid receptor binding + 0.6629 66.29%
Aromatase binding + 0.5527 55.27%
PPAR gamma + 0.5182 51.82%
Honey bee toxicity - 0.9392 93.92%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.9118 91.18%

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
CHEMBL2581 P07339 Cathepsin D 98.56% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.73% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.08% 85.14%
CHEMBL3359 P21462 Formyl peptide receptor 1 94.58% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 94.29% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.35% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.16% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.40% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.32% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 87.85% 90.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.36% 99.23%
CHEMBL3891 P07384 Calpain 1 84.71% 93.04%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.51% 81.11%
CHEMBL2535 P11166 Glucose transporter 84.47% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 84.18% 90.20%
CHEMBL1907 P15144 Aminopeptidase N 84.04% 93.31%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.29% 100.00%
CHEMBL5028 O14672 ADAM10 83.09% 97.50%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.86% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.72% 91.11%

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 139591600
LOTUS LTS0129855
wikiData Q104998497