10-Ethenyl-2,3,6,10,13,17,20,21-octamethyldocosa-1,6,11,16,21-pentaene

Details

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Internal ID 1d5e23bd-ccc2-47f4-9e63-0ac62b8e98dd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 10-ethenyl-2,3,6,10,13,17,20,21-octamethyldocosa-1,6,11,16,21-pentaene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H54/c1-12-32(11,23-14-17-28(7)19-21-31(10)26(4)5)24-22-29(8)16-13-15-27(6)18-20-30(9)25(2)3/h12,15,17,22,24,29-31H,1-2,4,13-14,16,18-21,23H2,3,5-11H3
InChI Key YIERDWVPDSIPLW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H54
Molecular Weight 438.80 g/mol
Exact Mass 438.422551722 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 12.90
Atomic LogP (AlogP) 10.81
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Ethenyl-2,3,6,10,13,17,20,21-octamethyldocosa-1,6,11,16,21-pentaene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9807 98.07%
Caco-2 - 0.6246 62.46%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.4721 47.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9020 90.20%
OATP1B3 inhibitior + 0.9208 92.08%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9168 91.68%
P-glycoprotein inhibitior + 0.8085 80.85%
P-glycoprotein substrate - 0.7364 73.64%
CYP3A4 substrate + 0.5108 51.08%
CYP2C9 substrate - 0.7980 79.80%
CYP2D6 substrate - 0.7751 77.51%
CYP3A4 inhibition - 0.9213 92.13%
CYP2C9 inhibition - 0.8640 86.40%
CYP2C19 inhibition - 0.8713 87.13%
CYP2D6 inhibition - 0.9430 94.30%
CYP1A2 inhibition - 0.7490 74.90%
CYP2C8 inhibition - 0.8669 86.69%
CYP inhibitory promiscuity - 0.7524 75.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Warning 0.4836 48.36%
Eye corrosion + 0.5816 58.16%
Eye irritation - 0.8995 89.95%
Skin irritation + 0.7547 75.47%
Skin corrosion - 0.9886 98.86%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8651 86.51%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.8993 89.93%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity + 0.5554 55.54%
Nephrotoxicity + 0.6459 64.59%
Acute Oral Toxicity (c) III 0.8895 88.95%
Estrogen receptor binding + 0.5340 53.40%
Androgen receptor binding - 0.5428 54.28%
Thyroid receptor binding + 0.6640 66.40%
Glucocorticoid receptor binding + 0.6122 61.22%
Aromatase binding + 0.5738 57.38%
PPAR gamma + 0.6485 64.85%
Honey bee toxicity - 0.7987 79.87%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9944 99.44%

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 94.90% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.03% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.73% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.18% 94.45%
CHEMBL236 P41143 Delta opioid receptor 82.19% 99.35%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.14% 93.56%
CHEMBL2885 P07451 Carbonic anhydrase III 81.70% 87.45%

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 77908831
LOTUS LTS0264393
wikiData Q105348792