16-Hydroxy-2,6,10,14-tetramethyl-2,6,10,14-hexadecatetraenoic acid

Details

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Internal ID 75315005-1deb-4bca-b078-f6a01302d72e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 16-hydroxy-2,6,10,14-tetramethylhexadeca-2,6,10,14-tetraenoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O3/c1-16(10-6-11-18(3)14-15-21)8-5-9-17(2)12-7-13-19(4)20(22)23/h9-10,13-14,21H,5-8,11-12,15H2,1-4H3,(H,22,23)
InChI Key CUIQJFFRKSRGBO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O3
Molecular Weight 320.50 g/mol
Exact Mass 320.23514488 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 5.30
Atomic LogP (AlogP) 5.19
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 11

Synonyms

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16-hydroxy-2,6,10,14-tetramethyl-2,6,10,14-hexadecatetraenoic acid

2D Structure

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2D Structure of 16-Hydroxy-2,6,10,14-tetramethyl-2,6,10,14-hexadecatetraenoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9724 97.24%
Caco-2 + 0.6706 67.06%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6215 62.15%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.9143 91.43%
OATP1B3 inhibitior + 0.9185 91.85%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.8667 86.67%
P-glycoprotein inhibitior - 0.6849 68.49%
P-glycoprotein substrate - 0.9704 97.04%
CYP3A4 substrate - 0.6090 60.90%
CYP2C9 substrate - 0.5754 57.54%
CYP2D6 substrate - 0.9111 91.11%
CYP3A4 inhibition - 0.8449 84.49%
CYP2C9 inhibition - 0.8242 82.42%
CYP2C19 inhibition - 0.8925 89.25%
CYP2D6 inhibition - 0.8735 87.35%
CYP1A2 inhibition - 0.7592 75.92%
CYP2C8 inhibition - 0.9535 95.35%
CYP inhibitory promiscuity - 0.8236 82.36%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6923 69.23%
Carcinogenicity (trinary) Non-required 0.6949 69.49%
Eye corrosion - 0.7307 73.07%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.5425 54.25%
Skin corrosion - 0.9788 97.88%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6942 69.42%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.5291 52.91%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.9034 90.34%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.5792 57.92%
Acute Oral Toxicity (c) III 0.7048 70.48%
Estrogen receptor binding + 0.5310 53.10%
Androgen receptor binding - 0.7154 71.54%
Thyroid receptor binding + 0.7304 73.04%
Glucocorticoid receptor binding + 0.5558 55.58%
Aromatase binding + 0.5538 55.38%
PPAR gamma + 0.8701 87.01%
Honey bee toxicity - 0.9734 97.34%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9782 97.82%

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 86.24% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.94% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.53% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.31% 91.11%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.08% 93.00%
CHEMBL340 P08684 Cytochrome P450 3A4 82.88% 91.19%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.66% 92.08%

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 53740698
LOTUS LTS0005025
wikiData Q104970291