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

Details

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Internal ID 3ab93e60-3398-4938-9dec-eea1dadc6a13
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 2-(4,8,12-trimethyltrideca-3,7,11-trienyl)but-2-ene-1,4-diol
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=CCO)CO)C)C)C
SMILES (Isomeric) CC(=CCCC(=CCCC(=CCCC(=CCO)CO)C)C)C
InChI InChI=1S/C20H34O2/c1-17(2)8-5-9-18(3)10-6-11-19(4)12-7-13-20(16-22)14-15-21/h8,10,12,14,21-22H,5-7,9,11,13,15-16H2,1-4H3
InChI Key GLWZBNMWNIPXEE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O2
Molecular Weight 306.50 g/mol
Exact Mass 306.255880323 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.10
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-(4,8,12-Trimethyltrideca-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 + 0.7773 77.73%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.4632 46.32%
OATP2B1 inhibitior - 0.8500 85.00%
OATP1B1 inhibitior + 0.9340 93.40%
OATP1B3 inhibitior + 0.9353 93.53%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7773 77.73%
P-glycoprotein inhibitior - 0.7566 75.66%
P-glycoprotein substrate - 0.9246 92.46%
CYP3A4 substrate - 0.5733 57.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
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 - 0.9622 96.22%
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 + 0.6405 64.05%
Skin irritation - 0.5862 58.62%
Skin corrosion - 0.9528 95.28%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6443 64.43%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation + 0.7769 77.69%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9420 94.20%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6221 62.21%
Acute Oral Toxicity (c) IV 0.6402 64.02%
Estrogen receptor binding - 0.5223 52.23%
Androgen receptor binding - 0.8008 80.08%
Thyroid receptor binding + 0.6004 60.04%
Glucocorticoid receptor binding - 0.6041 60.41%
Aromatase binding + 0.6174 61.74%
PPAR gamma + 0.8644 86.44%
Honey bee toxicity - 0.8882 88.82%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5800 58.00%
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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.50% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.01% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.13% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.67% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.34% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 81.28% 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.
Bejaranoa semistriata
Brickellia secundiflora

Cross-Links

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PubChem 85321918
LOTUS LTS0061713
wikiData Q105011400