2,12,16-Trihydroxy-2,6,10,14-tetramethylhexadeca-3,6,10,14-tetraen-5-one

Details

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Internal ID 5782f8b4-c4cc-466e-b884-8cd26151ad76
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 2,12,16-trihydroxy-2,6,10,14-tetramethylhexadeca-3,6,10,14-tetraen-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32O4/c1-15(13-18(22)14-16(2)10-12-21)7-6-8-17(3)19(23)9-11-20(4,5)24/h8-11,13,18,21-22,24H,6-7,12,14H2,1-5H3
InChI Key JHKUZYXDLVTBBJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O4
Molecular Weight 336.50 g/mol
Exact Mass 336.23005950 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.25
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,12,16-Trihydroxy-2,6,10,14-tetramethylhexadeca-3,6,10,14-tetraen-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9674 96.74%
Caco-2 + 0.5968 59.68%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7016 70.16%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.9143 91.43%
OATP1B3 inhibitior + 0.9371 93.71%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.8235 82.35%
P-glycoprotein inhibitior - 0.7030 70.30%
P-glycoprotein substrate - 0.6902 69.02%
CYP3A4 substrate + 0.5651 56.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8781 87.81%
CYP3A4 inhibition - 0.7440 74.40%
CYP2C9 inhibition - 0.8514 85.14%
CYP2C19 inhibition - 0.8955 89.55%
CYP2D6 inhibition - 0.9079 90.79%
CYP1A2 inhibition - 0.8047 80.47%
CYP2C8 inhibition - 0.8175 81.75%
CYP inhibitory promiscuity - 0.8494 84.94%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.7301 73.01%
Eye corrosion - 0.9385 93.85%
Eye irritation - 0.8393 83.93%
Skin irritation + 0.4892 48.92%
Skin corrosion - 0.9835 98.35%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4473 44.73%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation + 0.5695 56.95%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.5822 58.22%
Acute Oral Toxicity (c) III 0.7205 72.05%
Estrogen receptor binding + 0.6696 66.96%
Androgen receptor binding - 0.7301 73.01%
Thyroid receptor binding + 0.6841 68.41%
Glucocorticoid receptor binding + 0.6691 66.91%
Aromatase binding + 0.5399 53.99%
PPAR gamma + 0.7880 78.80%
Honey bee toxicity - 0.8568 85.68%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8619 86.19%

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
CHEMBL2581 P07339 Cathepsin D 94.97% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.83% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.18% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.20% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.62% 97.25%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 85.54% 98.75%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.43% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.31% 91.19%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.69% 85.14%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.92% 94.33%

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.
Ophryosporus floribundus

Cross-Links

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PubChem 163045824
LOTUS LTS0154658
wikiData Q105128040