Delicial

Details

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Internal ID f37a0ba4-2b16-4429-85fa-7b84f77347ed
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4-methyl-7-prop-1-en-2-yl-6,7-dihydroazulene-1-carbaldehyde
SMILES (Canonical) CC1=CCC(C=C2C1=CC=C2C=O)C(=C)C
SMILES (Isomeric) CC1=CCC(C=C2C1=CC=C2C=O)C(=C)C
InChI InChI=1S/C15H16O/c1-10(2)12-5-4-11(3)14-7-6-13(9-16)15(14)8-12/h4,6-9,12H,1,5H2,2-3H3
InChI Key XFQHUKCOVBABSG-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O
Molecular Weight 212.29 g/mol
Exact Mass 212.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.52
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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113393-58-1
DTXSID30921057
7-Isopropenyl-4-methyl-6,7-dihydro-1-azu
1-Azulenecarboxaldehyde, 6,7-dihydro-4-methyl-7-(1-methylethenyl)-
4-METHYL-7-(PROP-1-EN-2-YL)-6,7-DIHYDROAZULENE-1-CARBALDEHYDE

2D Structure

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2D Structure of Delicial

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.8742 87.42%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.7513 75.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9082 90.82%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5850 58.50%
P-glycoprotein inhibitior - 0.9370 93.70%
P-glycoprotein substrate - 0.8382 83.82%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.8279 82.79%
CYP3A4 inhibition - 0.8575 85.75%
CYP2C9 inhibition - 0.8723 87.23%
CYP2C19 inhibition - 0.7234 72.34%
CYP2D6 inhibition - 0.8611 86.11%
CYP1A2 inhibition - 0.6275 62.75%
CYP2C8 inhibition - 0.9071 90.71%
CYP inhibitory promiscuity - 0.8094 80.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6817 68.17%
Carcinogenicity (trinary) Non-required 0.6142 61.42%
Eye corrosion + 0.5758 57.58%
Eye irritation + 0.8175 81.75%
Skin irritation + 0.6687 66.87%
Skin corrosion - 0.7189 71.89%
Ames mutagenesis - 0.6228 62.28%
Human Ether-a-go-go-Related Gene inhibition + 0.6490 64.90%
Micronuclear - 0.7744 77.44%
Hepatotoxicity + 0.6301 63.01%
skin sensitisation + 0.8577 85.77%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.7571 75.71%
Acute Oral Toxicity (c) III 0.5833 58.33%
Estrogen receptor binding - 0.7307 73.07%
Androgen receptor binding - 0.6863 68.63%
Thyroid receptor binding - 0.6962 69.62%
Glucocorticoid receptor binding - 0.6990 69.90%
Aromatase binding - 0.6695 66.95%
PPAR gamma - 0.6609 66.09%
Honey bee toxicity - 0.8490 84.90%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9604 96.04%

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 90.54% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.74% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.03% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.74% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.24% 94.73%

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 181408
LOTUS LTS0024130
wikiData Q77518125