2-(6-methyl-3-methylidene-2-oxo-7-prop-1-en-2-yl-4,5,7,7a-tetrahydro-3aH-1-benzofuran-6-yl)acetaldehyde

Details

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Internal ID 072bbd14-6da4-47ae-ad27-ecac47d69957
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 2-(6-methyl-3-methylidene-2-oxo-7-prop-1-en-2-yl-4,5,7,7a-tetrahydro-3aH-1-benzofuran-6-yl)acetaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O3/c1-9(2)12-13-11(10(3)14(17)18-13)5-6-15(12,4)7-8-16/h8,11-13H,1,3,5-7H2,2,4H3
InChI Key SXEOWRCPPMKYMP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O3
Molecular Weight 248.32 g/mol
Exact Mass 248.14124450 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(6-methyl-3-methylidene-2-oxo-7-prop-1-en-2-yl-4,5,7,7a-tetrahydro-3aH-1-benzofuran-6-yl)acetaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9946 99.46%
Caco-2 + 0.6017 60.17%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6570 65.70%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.7781 77.81%
OATP1B3 inhibitior + 0.8899 88.99%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.9419 94.19%
P-glycoprotein inhibitior - 0.8637 86.37%
P-glycoprotein substrate - 0.7901 79.01%
CYP3A4 substrate + 0.5599 55.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8808 88.08%
CYP3A4 inhibition - 0.5859 58.59%
CYP2C9 inhibition - 0.9424 94.24%
CYP2C19 inhibition - 0.8384 83.84%
CYP2D6 inhibition - 0.9389 93.89%
CYP1A2 inhibition + 0.6234 62.34%
CYP2C8 inhibition - 0.7191 71.91%
CYP inhibitory promiscuity - 0.7968 79.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5637 56.37%
Eye corrosion - 0.9739 97.39%
Eye irritation - 0.6227 62.27%
Skin irritation + 0.5485 54.85%
Skin corrosion - 0.7682 76.82%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5157 51.57%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6628 66.28%
skin sensitisation + 0.5065 50.65%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.7352 73.52%
Acute Oral Toxicity (c) III 0.7370 73.70%
Estrogen receptor binding + 0.5951 59.51%
Androgen receptor binding + 0.5599 55.99%
Thyroid receptor binding - 0.6675 66.75%
Glucocorticoid receptor binding - 0.6228 62.28%
Aromatase binding - 0.7388 73.88%
PPAR gamma - 0.6344 63.44%
Honey bee toxicity - 0.8189 81.89%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9925 99.25%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.27% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.66% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.85% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.62% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.96% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.75% 100.00%
CHEMBL2581 P07339 Cathepsin D 83.61% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.88% 95.56%
CHEMBL1902 P62942 FK506-binding protein 1A 80.91% 97.05%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.78% 93.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.71% 89.00%

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 14355478
LOTUS LTS0111477
wikiData Q105263089