3,7,11,15-Tetramethylhexadeca-2,6,10,13,15-pentaen-1-ol

Details

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Internal ID 0c97e6ba-d82b-484f-99ab-5db12fb7078e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 3,7,11,15-tetramethylhexadeca-2,6,10,13,15-pentaen-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h6,9,11,13,15,21H,1,7-8,10,12,14,16H2,2-5H3
InChI Key JEMJHGRVHLIJQH-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O
Molecular Weight 288.50 g/mol
Exact Mass 288.245315640 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.70
Atomic LogP (AlogP) 5.90
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7,11,15-Tetramethylhexadeca-2,6,10,13,15-pentaen-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 + 0.9769 97.69%
Caco-2 + 0.8381 83.81%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.6614 66.14%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.9035 90.35%
OATP1B3 inhibitior + 0.9502 95.02%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7750 77.50%
P-glycoprotein inhibitior - 0.7076 70.76%
P-glycoprotein substrate - 0.9164 91.64%
CYP3A4 substrate - 0.5549 55.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7664 76.64%
CYP3A4 inhibition - 0.8176 81.76%
CYP2C9 inhibition - 0.8922 89.22%
CYP2C19 inhibition - 0.8768 87.68%
CYP2D6 inhibition - 0.9159 91.59%
CYP1A2 inhibition - 0.8476 84.76%
CYP2C8 inhibition - 0.8848 88.48%
CYP inhibitory promiscuity - 0.7908 79.08%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6635 66.35%
Eye corrosion + 0.5446 54.46%
Eye irritation + 0.6455 64.55%
Skin irritation + 0.7302 73.02%
Skin corrosion - 0.9538 95.38%
Ames mutagenesis - 0.6964 69.64%
Human Ether-a-go-go-Related Gene inhibition + 0.8565 85.65%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation + 0.8449 84.49%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6319 63.19%
Acute Oral Toxicity (c) III 0.8544 85.44%
Estrogen receptor binding - 0.6083 60.83%
Androgen receptor binding - 0.8217 82.17%
Thyroid receptor binding + 0.6658 66.58%
Glucocorticoid receptor binding - 0.4913 49.13%
Aromatase binding + 0.5832 58.32%
PPAR gamma + 0.8182 81.82%
Honey bee toxicity - 0.9018 90.18%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9694 96.94%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.44% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.45% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.27% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.07% 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 72727948
LOTUS LTS0003967
wikiData Q105126210