(E,3R,7S,11S)-3,7,11,15-tetramethylhexadec-1-en-1-ol

Details

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Internal ID 0d26af97-1d26-464a-a00c-aeb3ccad8e5d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name (E,3R,7S,11S)-3,7,11,15-tetramethylhexadec-1-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H40O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h15-21H,6-14H2,1-5H3/b16-15+/t18-,19-,20+/m0/s1
InChI Key BLUHKGOSFDHHGX-CTGNBOAYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H40O
Molecular Weight 296.50 g/mol
Exact Mass 296.307915895 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 8.70
Atomic LogP (AlogP) 7.13
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E,3R,7S,11S)-3,7,11,15-tetramethylhexadec-1-en-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 + 0.7956 79.56%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Lysosomes 0.3120 31.20%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9453 94.53%
OATP1B3 inhibitior + 0.9237 92.37%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.4718 47.18%
P-glycoprotein inhibitior - 0.8652 86.52%
P-glycoprotein substrate - 0.8210 82.10%
CYP3A4 substrate - 0.6293 62.93%
CYP2C9 substrate + 0.6107 61.07%
CYP2D6 substrate - 0.7961 79.61%
CYP3A4 inhibition - 0.9691 96.91%
CYP2C9 inhibition - 0.9101 91.01%
CYP2C19 inhibition - 0.9339 93.39%
CYP2D6 inhibition - 0.9589 95.89%
CYP1A2 inhibition - 0.7089 70.89%
CYP2C8 inhibition - 0.9681 96.81%
CYP inhibitory promiscuity - 0.8378 83.78%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6952 69.52%
Eye corrosion + 0.9279 92.79%
Eye irritation - 0.6370 63.70%
Skin irritation + 0.8188 81.88%
Skin corrosion - 0.9492 94.92%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4289 42.89%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.9631 96.31%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.8626 86.26%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7206 72.06%
Acute Oral Toxicity (c) III 0.8318 83.18%
Estrogen receptor binding - 0.6204 62.04%
Androgen receptor binding - 0.8968 89.68%
Thyroid receptor binding + 0.7468 74.68%
Glucocorticoid receptor binding + 0.5823 58.23%
Aromatase binding + 0.5239 52.39%
PPAR gamma - 0.5785 57.85%
Honey bee toxicity - 0.9723 97.23%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9705 97.05%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.52% 97.29%
CHEMBL2581 P07339 Cathepsin D 88.29% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.83% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 86.43% 87.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.02% 93.56%
CHEMBL226 P30542 Adenosine A1 receptor 84.04% 95.93%
CHEMBL1907 P15144 Aminopeptidase N 83.19% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.11% 99.17%

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 162912223
LOTUS LTS0149270
wikiData Q104938179