16-Hydroxy-2,6,10,14-tetramethylhexadeca-2,6,10,14-tetraen-4-one

Details

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Internal ID aadb91c9-fa61-4d48-860e-44c5b305ff44
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 16-hydroxy-2,6,10,14-tetramethylhexadeca-2,6,10,14-tetraen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O2/c1-16(2)14-20(22)15-19(5)11-7-9-17(3)8-6-10-18(4)12-13-21/h8,11-12,14,21H,6-7,9-10,13,15H2,1-5H3
InChI Key HJFXJURSUUYZPR-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O2
Molecular Weight 304.50 g/mol
Exact Mass 304.240230259 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.50
Atomic LogP (AlogP) 5.30
H-Bond Acceptor 2
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 16-Hydroxy-2,6,10,14-tetramethylhexadeca-2,6,10,14-tetraen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 + 0.8112 81.12%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6492 64.92%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.9385 93.85%
OATP1B3 inhibitior + 0.9363 93.63%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.8279 82.79%
P-glycoprotein inhibitior - 0.6679 66.79%
P-glycoprotein substrate - 0.8914 89.14%
CYP3A4 substrate - 0.5427 54.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8661 86.61%
CYP3A4 inhibition - 0.8678 86.78%
CYP2C9 inhibition - 0.8717 87.17%
CYP2C19 inhibition - 0.8688 86.88%
CYP2D6 inhibition - 0.9022 90.22%
CYP1A2 inhibition - 0.7213 72.13%
CYP2C8 inhibition - 0.9572 95.72%
CYP inhibitory promiscuity - 0.8106 81.06%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6968 69.68%
Eye corrosion - 0.6200 62.00%
Eye irritation + 0.5386 53.86%
Skin irritation + 0.6573 65.73%
Skin corrosion - 0.9727 97.27%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7498 74.98%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation + 0.7936 79.36%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6400 64.00%
Acute Oral Toxicity (c) III 0.7668 76.68%
Estrogen receptor binding - 0.6635 66.35%
Androgen receptor binding - 0.6982 69.82%
Thyroid receptor binding + 0.5742 57.42%
Glucocorticoid receptor binding - 0.5839 58.39%
Aromatase binding - 0.4824 48.24%
PPAR gamma + 0.7655 76.55%
Honey bee toxicity - 0.9398 93.98%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.8209 82.09%

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 90.85% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.77% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.41% 89.34%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.40% 94.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.75% 91.11%
CHEMBL2581 P07339 Cathepsin D 82.84% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 80.69% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 80.16% 91.19%

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 128931
LOTUS LTS0088622
wikiData Q105029225