11-O-Methylisocorniculatolide A

Details

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Internal ID be7b9a3e-4273-44eb-a739-b94eb0da19dc
Taxonomy Lignans, neolignans and related compounds > Lignan lactones
IUPAC Name 4-methoxy-2,11-dioxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),15,18-hexaen-12-one
SMILES (Canonical) COC1=C2C=C(CCCOC(=O)CCC3=CC=C(O2)C=C3)C=C1
SMILES (Isomeric) COC1=C2C=C(CCCOC(=O)CCC3=CC=C(O2)C=C3)C=C1
InChI InChI=1S/C19H20O4/c1-21-17-10-6-15-3-2-12-22-19(20)11-7-14-4-8-16(9-5-14)23-18(17)13-15/h4-6,8-10,13H,2-3,7,11-12H2,1H3
InChI Key OKZFWXLVYRFSKD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H20O4
Molecular Weight 312.40 g/mol
Exact Mass 312.13615911 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.91
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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CHEMBL2012175

2D Structure

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2D Structure of 11-O-Methylisocorniculatolide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 + 0.8791 87.91%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8828 88.28%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.9492 94.92%
OATP1B3 inhibitior + 0.9638 96.38%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9709 97.09%
P-glycoprotein inhibitior + 0.6174 61.74%
P-glycoprotein substrate - 0.8723 87.23%
CYP3A4 substrate + 0.5141 51.41%
CYP2C9 substrate + 0.5853 58.53%
CYP2D6 substrate - 0.7664 76.64%
CYP3A4 inhibition - 0.7934 79.34%
CYP2C9 inhibition - 0.5361 53.61%
CYP2C19 inhibition + 0.7507 75.07%
CYP2D6 inhibition - 0.8687 86.87%
CYP1A2 inhibition + 0.7874 78.74%
CYP2C8 inhibition - 0.7915 79.15%
CYP inhibitory promiscuity - 0.6534 65.34%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5674 56.74%
Eye corrosion - 0.9530 95.30%
Eye irritation - 0.5717 57.17%
Skin irritation - 0.8657 86.57%
Skin corrosion - 0.9888 98.88%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8327 83.27%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8721 87.21%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.6161 61.61%
Acute Oral Toxicity (c) III 0.7029 70.29%
Estrogen receptor binding + 0.8154 81.54%
Androgen receptor binding + 0.6762 67.62%
Thyroid receptor binding + 0.5705 57.05%
Glucocorticoid receptor binding + 0.6584 65.84%
Aromatase binding + 0.7584 75.84%
PPAR gamma - 0.5956 59.56%
Honey bee toxicity - 0.9036 90.36%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9291 92.91%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.89% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.55% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.50% 94.45%
CHEMBL2581 P07339 Cathepsin D 90.54% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.25% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.02% 91.11%
CHEMBL2535 P11166 Glucose transporter 87.60% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.25% 94.00%
CHEMBL4208 P20618 Proteasome component C5 85.62% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.95% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.36% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.55% 93.99%

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.
Aegiceras corniculatum

Cross-Links

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PubChem 57331849
NPASS NPC208608
LOTUS LTS0036083
wikiData Q105193840