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

Details

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Internal ID 90d6654d-4186-475a-ace5-bfbba040c61d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (5-acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl) acetate
SMILES (Canonical) CC(=CC(C(C(=CCCC(C)(C=C)O)C)OC(=O)C)OC(=O)C)C
SMILES (Isomeric) CC(=CC(C(C(=CCCC(C)(C=C)O)C)OC(=O)C)OC(=O)C)C
InChI InChI=1S/C19H30O5/c1-8-19(7,22)11-9-10-14(4)18(24-16(6)21)17(12-13(2)3)23-15(5)20/h8,10,12,17-18,22H,1,9,11H2,2-7H3
InChI Key HRCVDYKTTYCITA-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 (5-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 + 0.9640 96.40%
Caco-2 + 0.6420 64.20%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.6399 63.99%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9197 91.97%
OATP1B3 inhibitior + 0.9330 93.30%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5316 53.16%
P-glycoprotein inhibitior - 0.6333 63.33%
P-glycoprotein substrate - 0.8512 85.12%
CYP3A4 substrate + 0.5878 58.78%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8754 87.54%
CYP3A4 inhibition - 0.6754 67.54%
CYP2C9 inhibition - 0.8170 81.70%
CYP2C19 inhibition - 0.8610 86.10%
CYP2D6 inhibition - 0.9330 93.30%
CYP1A2 inhibition - 0.8528 85.28%
CYP2C8 inhibition - 0.7262 72.62%
CYP inhibitory promiscuity - 0.9446 94.46%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6215 62.15%
Carcinogenicity (trinary) Non-required 0.6872 68.72%
Eye corrosion - 0.8419 84.19%
Eye irritation - 0.6431 64.31%
Skin irritation + 0.6462 64.62%
Skin corrosion - 0.9349 93.49%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5603 56.03%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.5737 57.37%
skin sensitisation + 0.7635 76.35%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.8309 83.09%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.6472 64.72%
Acute Oral Toxicity (c) IV 0.5654 56.54%
Estrogen receptor binding - 0.5053 50.53%
Androgen receptor binding - 0.6342 63.42%
Thyroid receptor binding - 0.5571 55.71%
Glucocorticoid receptor binding + 0.5435 54.35%
Aromatase binding - 0.5622 56.22%
PPAR gamma - 0.5000 50.00%
Honey bee toxicity - 0.6544 65.44%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9354 93.54%

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
CHEMBL2581 P07339 Cathepsin D 93.04% 98.95%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 90.72% 90.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.52% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.72% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.82% 97.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.64% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 85.71% 94.73%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 85.24% 97.47%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.10% 96.47%
CHEMBL3437 Q16853 Amine oxidase, copper containing 80.22% 94.00%

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.
Hedychium coronarium

Cross-Links

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PubChem 85101661
LOTUS LTS0110881
wikiData Q105032576