Venezueline C

Details

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Internal ID 7cea3528-c4d8-4775-9ca0-df2ec6060591
Taxonomy Organoheterocyclic compounds > Benzoxazines > Phenoxazines
IUPAC Name [2-acetamido-8-(hydroxymethyl)-10H-phenoxazin-3-yl] 2-hydroxyacetate
SMILES (Canonical) CC(=O)NC1=C(C=C2C(=C1)NC3=C(O2)C=CC(=C3)CO)OC(=O)CO
SMILES (Isomeric) CC(=O)NC1=C(C=C2C(=C1)NC3=C(O2)C=CC(=C3)CO)OC(=O)CO
InChI InChI=1S/C17H16N2O6/c1-9(22)18-12-5-13-15(6-16(12)25-17(23)8-21)24-14-3-2-10(7-20)4-11(14)19-13/h2-6,19-21H,7-8H2,1H3,(H,18,22)
InChI Key OMNPWACYOUMUON-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H16N2O6
Molecular Weight 344.32 g/mol
Exact Mass 344.10083623 g/mol
Topological Polar Surface Area (TPSA) 117.00 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.88
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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Vnezueline C
CHEMBL2311992

2D Structure

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2D Structure of Venezueline C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7959 79.59%
Caco-2 - 0.7529 75.29%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Nucleus 0.3573 35.73%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.8879 88.79%
OATP1B3 inhibitior + 0.9417 94.17%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9054 90.54%
P-glycoprotein inhibitior - 0.8398 83.98%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.5811 58.11%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.7696 76.96%
CYP3A4 inhibition - 0.7650 76.50%
CYP2C9 inhibition - 0.5779 57.79%
CYP2C19 inhibition - 0.6898 68.98%
CYP2D6 inhibition - 0.8946 89.46%
CYP1A2 inhibition - 0.7391 73.91%
CYP2C8 inhibition - 0.5655 56.55%
CYP inhibitory promiscuity + 0.5516 55.16%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6793 67.93%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9277 92.77%
Skin irritation - 0.8456 84.56%
Skin corrosion - 0.9578 95.78%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6649 66.49%
Micronuclear + 0.8700 87.00%
Hepatotoxicity - 0.5603 56.03%
skin sensitisation - 0.9151 91.51%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.6532 65.32%
Acute Oral Toxicity (c) III 0.6550 65.50%
Estrogen receptor binding + 0.9226 92.26%
Androgen receptor binding + 0.5917 59.17%
Thyroid receptor binding + 0.6006 60.06%
Glucocorticoid receptor binding + 0.8848 88.48%
Aromatase binding + 0.7438 74.38%
PPAR gamma + 0.7893 78.93%
Honey bee toxicity - 0.7428 74.28%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5399 53.99%
Fish aquatic toxicity - 0.4653 46.53%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.32% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.97% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.54% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.92% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.01% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.83% 95.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.62% 94.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 88.55% 89.50%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 86.42% 95.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.10% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.00% 89.00%
CHEMBL1255126 O15151 Protein Mdm4 85.05% 90.20%
CHEMBL4208 P20618 Proteasome component C5 84.56% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.02% 96.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.94% 94.80%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.56% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.07% 96.00%
CHEMBL2535 P11166 Glucose transporter 81.60% 98.75%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.35% 96.90%
CHEMBL340 P08684 Cytochrome P450 3A4 80.09% 91.19%

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 71517221
LOTUS LTS0038771
wikiData Q77386901