(8-Acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl) acetate

Details

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Internal ID dde7d438-1a91-4556-9c26-482e29c08af4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (8-acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl) acetate
SMILES (Canonical) CC(=CC(CC(=CC(CC(C)(C=C)O)OC(=O)C)C)OC(=O)C)C
SMILES (Isomeric) CC(=CC(CC(=CC(CC(C)(C=C)O)OC(=O)C)C)OC(=O)C)C
InChI InChI=1S/C19H30O5/c1-8-19(7,22)12-18(24-16(6)21)11-14(4)10-17(9-13(2)3)23-15(5)20/h8-9,11,17-18,22H,1,10,12H2,2-7H3
InChI Key ZWCHRIPZSGWZAL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H30O5
Molecular Weight 338.40 g/mol
Exact Mass 338.20932405 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8-Acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9605 96.05%
Caco-2 + 0.5082 50.82%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7323 73.23%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.9229 92.29%
OATP1B3 inhibitior + 0.9264 92.64%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.7213 72.13%
P-glycoprotein substrate - 0.9028 90.28%
CYP3A4 substrate + 0.5479 54.79%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8754 87.54%
CYP3A4 inhibition - 0.6930 69.30%
CYP2C9 inhibition - 0.8071 80.71%
CYP2C19 inhibition - 0.7558 75.58%
CYP2D6 inhibition - 0.9496 94.96%
CYP1A2 inhibition - 0.9169 91.69%
CYP2C8 inhibition - 0.7728 77.28%
CYP inhibitory promiscuity - 0.9412 94.12%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) + 0.5285 52.85%
Carcinogenicity (trinary) Non-required 0.6255 62.55%
Eye corrosion - 0.7756 77.56%
Eye irritation - 0.4857 48.57%
Skin irritation + 0.5807 58.07%
Skin corrosion - 0.9581 95.81%
Ames mutagenesis - 0.6528 65.28%
Human Ether-a-go-go-Related Gene inhibition - 0.7184 71.84%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5407 54.07%
skin sensitisation + 0.7162 71.62%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.8309 83.09%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6450 64.50%
Acute Oral Toxicity (c) III 0.6019 60.19%
Estrogen receptor binding - 0.6662 66.62%
Androgen receptor binding - 0.6269 62.69%
Thyroid receptor binding - 0.5497 54.97%
Glucocorticoid receptor binding + 0.5426 54.26%
Aromatase binding - 0.5067 50.67%
PPAR gamma - 0.5173 51.73%
Honey bee toxicity - 0.6977 69.77%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9596 95.96%

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
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 95.01% 90.93%
CHEMBL2581 P07339 Cathepsin D 94.97% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 93.00% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 92.68% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.15% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 91.71% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.40% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.68% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 86.05% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.61% 94.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.40% 93.56%

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.
Achillea nobilis
Santolina oblongifolia

Cross-Links

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PubChem 163040517
LOTUS LTS0009661
wikiData Q105384820