2-(4,8,10,12-Tetramethyltrideca-3,7,11-trienyl)but-2-ene-1,4-diol

Details

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Internal ID a46b7282-222a-45e1-98d1-8f8f15b39744
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 2-(4,8,10,12-tetramethyltrideca-3,7,11-trienyl)but-2-ene-1,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H36O2/c1-17(2)14-20(5)15-19(4)10-6-8-18(3)9-7-11-21(16-23)12-13-22/h9-10,12,14,20,22-23H,6-8,11,13,15-16H2,1-5H3
InChI Key OIMAKPRCKIKPRX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H36O2
Molecular Weight 320.50 g/mol
Exact Mass 320.271530387 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 5.70
Atomic LogP (AlogP) 5.34
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(4,8,10,12-Tetramethyltrideca-3,7,11-trienyl)but-2-ene-1,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9770 97.70%
Caco-2 + 0.6911 69.11%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Lysosomes 0.4632 46.32%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.8997 89.97%
OATP1B3 inhibitior + 0.9353 93.53%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7620 76.20%
P-glycoprotein inhibitior - 0.6161 61.61%
P-glycoprotein substrate - 0.8150 81.50%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6591 65.91%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.8614 86.14%
CYP2C9 inhibition - 0.8689 86.89%
CYP2C19 inhibition - 0.8773 87.73%
CYP2D6 inhibition - 0.9119 91.19%
CYP1A2 inhibition - 0.8663 86.63%
CYP2C8 inhibition - 0.9063 90.63%
CYP inhibitory promiscuity - 0.8063 80.63%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.6428 64.28%
Eye corrosion + 0.4493 44.93%
Eye irritation - 0.7545 75.45%
Skin irritation - 0.5862 58.62%
Skin corrosion - 0.9528 95.28%
Ames mutagenesis - 0.6737 67.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7199 71.99%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation + 0.7769 77.69%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.9420 94.20%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.5507 55.07%
Acute Oral Toxicity (c) IV 0.6402 64.02%
Estrogen receptor binding - 0.4771 47.71%
Androgen receptor binding - 0.7404 74.04%
Thyroid receptor binding + 0.5715 57.15%
Glucocorticoid receptor binding - 0.5416 54.16%
Aromatase binding + 0.5541 55.41%
PPAR gamma + 0.8233 82.33%
Honey bee toxicity - 0.8103 81.03%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9391 93.91%

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 90.35% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.64% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.64% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.92% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.55% 91.11%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 83.08% 93.10%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 81.77% 97.23%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.78% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 80.45% 94.73%

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.
Disynaphia halimifolia

Cross-Links

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PubChem 162914251
LOTUS LTS0269255
wikiData Q105192598