16-Hydroxy-2,10,14-trimethyl-6-methylidenehexadeca-2,10,14-triene-4,7-dione

Details

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Internal ID 6a85ae9f-9fc6-4cb4-aaa6-87c806158451
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 16-hydroxy-2,10,14-trimethyl-6-methylidenehexadeca-2,10,14-triene-4,7-dione
SMILES (Canonical) CC(=CC(=O)CC(=C)C(=O)CCC(=CCCC(=CCO)C)C)C
SMILES (Isomeric) CC(=CC(=O)CC(=C)C(=O)CCC(=CCCC(=CCO)C)C)C
InChI InChI=1S/C20H30O3/c1-15(2)13-19(22)14-18(5)20(23)10-9-16(3)7-6-8-17(4)11-12-21/h7,11,13,21H,5-6,8-10,12,14H2,1-4H3
InChI Key KCBUEVHZHDNVJS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O3
Molecular Weight 318.40 g/mol
Exact Mass 318.21949481 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.48
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 16-Hydroxy-2,10,14-trimethyl-6-methylidenehexadeca-2,10,14-triene-4,7-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9747 97.47%
Caco-2 + 0.7623 76.23%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7736 77.36%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.9235 92.35%
OATP1B3 inhibitior + 0.9435 94.35%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.8079 80.79%
P-glycoprotein inhibitior - 0.6913 69.13%
P-glycoprotein substrate - 0.8365 83.65%
CYP3A4 substrate + 0.5091 50.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8661 86.61%
CYP3A4 inhibition - 0.5425 54.25%
CYP2C9 inhibition - 0.7640 76.40%
CYP2C19 inhibition - 0.8088 80.88%
CYP2D6 inhibition - 0.8668 86.68%
CYP1A2 inhibition - 0.7113 71.13%
CYP2C8 inhibition - 0.9108 91.08%
CYP inhibitory promiscuity - 0.8707 87.07%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6623 66.23%
Carcinogenicity (trinary) Non-required 0.7121 71.21%
Eye corrosion - 0.7940 79.40%
Eye irritation - 0.7386 73.86%
Skin irritation + 0.5932 59.32%
Skin corrosion - 0.9690 96.90%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7488 74.88%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation + 0.6443 64.43%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.6174 61.74%
Acute Oral Toxicity (c) III 0.7537 75.37%
Estrogen receptor binding - 0.7248 72.48%
Androgen receptor binding - 0.5983 59.83%
Thyroid receptor binding - 0.4914 49.14%
Glucocorticoid receptor binding - 0.5366 53.66%
Aromatase binding - 0.5576 55.76%
PPAR gamma + 0.7846 78.46%
Honey bee toxicity - 0.8976 89.76%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9623 96.23%

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 88.81% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.48% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 87.06% 94.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.67% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 84.10% 83.82%
CHEMBL2581 P07339 Cathepsin D 83.85% 98.95%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.73% 91.24%
CHEMBL340 P08684 Cytochrome P450 3A4 83.33% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 81.66% 94.73%

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 163043027
LOTUS LTS0150183
wikiData Q105138663