Phenaziterpene A

Details

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Internal ID 24a01a40-927d-4cc2-81ab-972223f43f85
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name 6-[(2E)-3,7-dimethylocta-2,6-dienoxy]phenazin-1-ol
SMILES (Canonical) CC(=CCCC(=CCOC1=CC=CC2=NC3=C(C=CC=C3O)N=C21)C)C
SMILES (Isomeric) CC(=CCC/C(=C/COC1=CC=CC2=NC3=C(C=CC=C3O)N=C21)/C)C
InChI InChI=1S/C22H24N2O2/c1-15(2)7-4-8-16(3)13-14-26-20-12-6-10-18-22(20)24-17-9-5-11-19(25)21(17)23-18/h5-7,9-13,25H,4,8,14H2,1-3H3/b16-13+
InChI Key GTZWCZPREISNMM-DTQAZKPQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H24N2O2
Molecular Weight 348.40 g/mol
Exact Mass 348.183778013 g/mol
Topological Polar Surface Area (TPSA) 55.20 Ų
XlogP 5.60
Atomic LogP (AlogP) 5.56
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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CHEMBL3092700

2D Structure

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2D Structure of Phenaziterpene A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 - 0.6273 62.73%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7703 77.03%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.9479 94.79%
OATP1B3 inhibitior + 0.9288 92.88%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.9796 97.96%
P-glycoprotein inhibitior + 0.6771 67.71%
P-glycoprotein substrate - 0.8287 82.87%
CYP3A4 substrate + 0.5411 54.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7034 70.34%
CYP3A4 inhibition + 0.6020 60.20%
CYP2C9 inhibition - 0.6443 64.43%
CYP2C19 inhibition + 0.5880 58.80%
CYP2D6 inhibition - 0.7972 79.72%
CYP1A2 inhibition + 0.7271 72.71%
CYP2C8 inhibition + 0.6302 63.02%
CYP inhibitory promiscuity + 0.6270 62.70%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9630 96.30%
Carcinogenicity (trinary) Non-required 0.6896 68.96%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.8740 87.40%
Skin irritation - 0.7978 79.78%
Skin corrosion - 0.9363 93.63%
Ames mutagenesis + 0.5346 53.46%
Human Ether-a-go-go-Related Gene inhibition + 0.8283 82.83%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.7819 78.19%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.6209 62.09%
Acute Oral Toxicity (c) III 0.7377 73.77%
Estrogen receptor binding + 0.8730 87.30%
Androgen receptor binding + 0.7303 73.03%
Thyroid receptor binding + 0.7319 73.19%
Glucocorticoid receptor binding + 0.8435 84.35%
Aromatase binding + 0.7575 75.75%
PPAR gamma + 0.8707 87.07%
Honey bee toxicity - 0.9101 91.01%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9409 94.09%

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
CHEMBL1937 Q92769 Histone deacetylase 2 94.73% 94.75%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 93.43% 93.10%
CHEMBL3401 O75469 Pregnane X receptor 93.34% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.28% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.22% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.04% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.67% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.02% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.14% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.87% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.64% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.57% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.33% 95.50%
CHEMBL3891 P07384 Calpain 1 82.21% 93.04%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.30% 95.56%
CHEMBL2039 P27338 Monoamine oxidase B 80.18% 92.51%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 136264440
LOTUS LTS0265562
wikiData Q77564720