14-(Hydroxymethyl)-2,6,10-trimethylhexadeca-2,6,10,14-tetraene-1,16-diol

Details

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Internal ID d955f69e-a30c-4d67-9613-9add3e95d788
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 14-(hydroxymethyl)-2,6,10-trimethylhexadeca-2,6,10,14-tetraene-1,16-diol
SMILES (Canonical) CC(=CCCC(=CCO)CO)CCC=C(C)CCC=C(C)CO
SMILES (Isomeric) CC(=CCCC(=CCO)CO)CCC=C(C)CCC=C(C)CO
InChI InChI=1S/C20H34O3/c1-17(9-5-11-19(3)15-22)7-4-8-18(2)10-6-12-20(16-23)13-14-21/h7,10-11,13,21-23H,4-6,8-9,12,14-16H2,1-3H3
InChI Key FXAGOBAZVGQRIS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O3
Molecular Weight 322.50 g/mol
Exact Mass 322.25079494 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.07
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 14-(Hydroxymethyl)-2,6,10-trimethylhexadeca-2,6,10,14-tetraene-1,16-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9638 96.38%
Caco-2 + 0.6766 67.66%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.4512 45.12%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.9302 93.02%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8143 81.43%
BSEP inhibitior + 0.7928 79.28%
P-glycoprotein inhibitior - 0.7636 76.36%
P-glycoprotein substrate - 0.9076 90.76%
CYP3A4 substrate - 0.5805 58.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.7359 73.59%
CYP2C9 inhibition - 0.8543 85.43%
CYP2C19 inhibition - 0.8685 86.85%
CYP2D6 inhibition - 0.8843 88.43%
CYP1A2 inhibition - 0.8417 84.17%
CYP2C8 inhibition - 0.9506 95.06%
CYP inhibitory promiscuity - 0.8218 82.18%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7123 71.23%
Carcinogenicity (trinary) Non-required 0.6493 64.93%
Eye corrosion - 0.7011 70.11%
Eye irritation + 0.5771 57.71%
Skin irritation - 0.7492 74.92%
Skin corrosion - 0.9728 97.28%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6474 64.74%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation + 0.5680 56.80%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.9479 94.79%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.5760 57.60%
Acute Oral Toxicity (c) IV 0.6382 63.82%
Estrogen receptor binding + 0.6162 61.62%
Androgen receptor binding - 0.7981 79.81%
Thyroid receptor binding + 0.6938 69.38%
Glucocorticoid receptor binding - 0.4914 49.14%
Aromatase binding + 0.6357 63.57%
PPAR gamma + 0.8589 85.89%
Honey bee toxicity - 0.9080 90.80%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9446 94.46%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.86% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.26% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.06% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.42% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.63% 91.11%

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.
Bejaranoa semistriata
Tithonia diversifolia

Cross-Links

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PubChem 74208353
LOTUS LTS0220218
wikiData Q105003793