4-(3,7-Dimethylocta-2,6-dienyl)-3,5-dihydroxybenzaldehyde

Details

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Internal ID faade1e4-d813-46fa-a412-064a1dd397d7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name 4-(3,7-dimethylocta-2,6-dienyl)-3,5-dihydroxybenzaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O3/c1-12(2)5-4-6-13(3)7-8-15-16(19)9-14(11-18)10-17(15)20/h5,7,9-11,19-20H,4,6,8H2,1-3H3
InChI Key YMZBLCOCJILVMY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O3
Molecular Weight 274.35 g/mol
Exact Mass 274.15689456 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(3,7-Dimethylocta-2,6-dienyl)-3,5-dihydroxybenzaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.7075 70.75%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8470 84.70%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.8318 83.18%
OATP1B3 inhibitior + 0.9308 93.08%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.5513 55.13%
P-glycoprotein inhibitior - 0.8354 83.54%
P-glycoprotein substrate - 0.9355 93.55%
CYP3A4 substrate - 0.5997 59.97%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7184 71.84%
CYP3A4 inhibition + 0.7019 70.19%
CYP2C9 inhibition + 0.7248 72.48%
CYP2C19 inhibition + 0.6909 69.09%
CYP2D6 inhibition - 0.7856 78.56%
CYP1A2 inhibition + 0.8525 85.25%
CYP2C8 inhibition - 0.8853 88.53%
CYP inhibitory promiscuity + 0.6656 66.56%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8162 81.62%
Carcinogenicity (trinary) Non-required 0.7050 70.50%
Eye corrosion - 0.9693 96.93%
Eye irritation + 0.6509 65.09%
Skin irritation - 0.6522 65.22%
Skin corrosion - 0.9136 91.36%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4114 41.14%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.7007 70.07%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.5588 55.88%
Acute Oral Toxicity (c) III 0.6061 60.61%
Estrogen receptor binding + 0.6993 69.93%
Androgen receptor binding + 0.5689 56.89%
Thyroid receptor binding + 0.5480 54.80%
Glucocorticoid receptor binding + 0.7908 79.08%
Aromatase binding + 0.6875 68.75%
PPAR gamma + 0.9246 92.46%
Honey bee toxicity - 0.9209 92.09%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 1.0000 100.00%

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 96.48% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 95.84% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 93.77% 94.73%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 91.86% 98.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.70% 92.08%
CHEMBL2581 P07339 Cathepsin D 91.58% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.87% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.29% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.12% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.56% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.49% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.20% 86.33%
CHEMBL4208 P20618 Proteasome component C5 81.03% 90.00%

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.
Milicia excelsa

Cross-Links

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PubChem 163005922
LOTUS LTS0008414
wikiData Q105350820