3,4,5,6-Tetrahydro-2-oxo-2h-1,6-benzoxazocine-8-carboxylic acid

Details

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Internal ID cf5ab48f-d4e9-43f9-b54c-fa688a400618
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Amines > Secondary amines > Secondary alkylarylamines
IUPAC Name 2-oxo-3,4,5,6-tetrahydro-1,6-benzoxazocine-8-carboxylic acid
SMILES (Canonical) C1CC(=O)OC2=C(C=C(C=C2)C(=O)O)NC1
SMILES (Isomeric) C1CC(=O)OC2=C(C=C(C=C2)C(=O)O)NC1
InChI InChI=1S/C11H11NO4/c13-10-2-1-5-12-8-6-7(11(14)15)3-4-9(8)16-10/h3-4,6,12H,1-2,5H2,(H,14,15)
InChI Key QWQBHSVBSAZDQN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H11NO4
Molecular Weight 221.21 g/mol
Exact Mass 221.06880783 g/mol
Topological Polar Surface Area (TPSA) 75.60 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.50
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,4,5,6-Tetrahydro-2-oxo-2h-1,6-benzoxazocine-8-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9848 98.48%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5226 52.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9545 95.45%
OATP1B3 inhibitior + 0.9440 94.40%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9820 98.20%
P-glycoprotein inhibitior - 0.9865 98.65%
P-glycoprotein substrate - 0.9434 94.34%
CYP3A4 substrate - 0.6219 62.19%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.7478 74.78%
CYP3A4 inhibition - 0.9804 98.04%
CYP2C9 inhibition - 0.9334 93.34%
CYP2C19 inhibition - 0.8423 84.23%
CYP2D6 inhibition - 0.9127 91.27%
CYP1A2 inhibition - 0.6500 65.00%
CYP2C8 inhibition - 0.8648 86.48%
CYP inhibitory promiscuity - 0.9933 99.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.7256 72.56%
Eye corrosion - 0.9874 98.74%
Eye irritation + 0.8631 86.31%
Skin irritation - 0.7754 77.54%
Skin corrosion - 0.9412 94.12%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7965 79.65%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8219 82.19%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7635 76.35%
Acute Oral Toxicity (c) III 0.6515 65.15%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.7324 73.24%
Thyroid receptor binding - 0.6532 65.32%
Glucocorticoid receptor binding - 0.7698 76.98%
Aromatase binding + 0.5468 54.68%
PPAR gamma + 0.8047 80.47%
Honey bee toxicity - 0.9665 96.65%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.9052 90.52%
Fish aquatic toxicity - 0.8791 87.91%

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 94.47% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.19% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.91% 91.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 89.62% 87.67%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.12% 93.99%
CHEMBL4208 P20618 Proteasome component C5 86.75% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.60% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.30% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.10% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.71% 90.71%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 81.52% 95.48%

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.
Argania spinosa

Cross-Links

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PubChem 138455241
LOTUS LTS0057700
wikiData Q105229328