3,7,11,15-Tetramethylhexadeca-2,6,10,12,14-pentaen-1-ol

Details

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Internal ID 2235675c-9a33-4827-ad79-0dc26dbfe1d2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 3,7,11,15-tetramethylhexadeca-2,6,10,12,14-pentaen-1-ol
SMILES (Canonical) CC(=CC=CC(=CCCC(=CCCC(=CCO)C)C)C)C
SMILES (Isomeric) CC(=CC=CC(=CCCC(=CCCC(=CCO)C)C)C)C
InChI InChI=1S/C20H32O/c1-17(2)9-6-10-18(3)11-7-12-19(4)13-8-14-20(5)15-16-21/h6,9-11,13,15,21H,7-8,12,14,16H2,1-5H3
InChI Key OTYIYOOKHMFXBC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O
Molecular Weight 288.50 g/mol
Exact Mass 288.245315640 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.70
Atomic LogP (AlogP) 5.90
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7,11,15-Tetramethylhexadeca-2,6,10,12,14-pentaen-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.9198 91.98%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.5576 55.76%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.8994 89.94%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7816 78.16%
P-glycoprotein inhibitior - 0.7011 70.11%
P-glycoprotein substrate - 0.9048 90.48%
CYP3A4 substrate - 0.5164 51.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7664 76.64%
CYP3A4 inhibition - 0.9088 90.88%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.9138 91.38%
CYP inhibitory promiscuity - 0.7650 76.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion + 0.5325 53.25%
Eye irritation + 0.6006 60.06%
Skin irritation + 0.8492 84.92%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7799 77.99%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7051 70.51%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9812 98.12%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6495 64.95%
Acute Oral Toxicity (c) III 0.8552 85.52%
Estrogen receptor binding - 0.5176 51.76%
Androgen receptor binding - 0.8499 84.99%
Thyroid receptor binding + 0.6688 66.88%
Glucocorticoid receptor binding - 0.5568 55.68%
Aromatase binding + 0.6831 68.31%
PPAR gamma + 0.8031 80.31%
Honey bee toxicity - 0.9334 93.34%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9500 95.00%

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
CHEMBL4040 P28482 MAP kinase ERK2 89.37% 83.82%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.96% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.99% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.90% 99.17%
CHEMBL2581 P07339 Cathepsin D 80.55% 98.95%

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.
Saururus cernuus

Cross-Links

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PubChem 85151945
LOTUS LTS0058649
wikiData Q105199927