(4E,8Z,12Z,16E)-5,9,13,17,21-pentamethyl-2-prop-1-en-2-yldocosa-4,8,12,16,20-pentaen-1-ol

Details

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Internal ID fbe07931-9b0f-4b58-a34c-12419a393a31
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids
IUPAC Name (4E,8Z,12Z,16E)-5,9,13,17,21-pentamethyl-2-prop-1-en-2-yldocosa-4,8,12,16,20-pentaen-1-ol
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCC(CO)C(=C)C)C)C)C)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CC/C(=C\CC/C(=C\CC/C(=C/CC(CO)C(=C)C)/C)/C)/C)/C)C
InChI InChI=1S/C30H50O/c1-24(2)13-9-14-26(5)15-10-16-27(6)17-11-18-28(7)19-12-20-29(8)21-22-30(23-31)25(3)4/h13,15,17,19,21,30-31H,3,9-12,14,16,18,20,22-23H2,1-2,4-8H3/b26-15+,27-17-,28-19-,29-21+
InChI Key OMSQHPKNHFHAKB-NVRDDEHMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O
Molecular Weight 426.70 g/mol
Exact Mass 426.386166214 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 10.50
Atomic LogP (AlogP) 9.43
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4E,8Z,12Z,16E)-5,9,13,17,21-pentamethyl-2-prop-1-en-2-yldocosa-4,8,12,16,20-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 + 0.9893 98.93%
Caco-2 - 0.6209 62.09%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.5603 56.03%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.9359 93.59%
OATP1B3 inhibitior + 0.9358 93.58%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8667 86.67%
P-glycoprotein inhibitior + 0.7726 77.26%
P-glycoprotein substrate - 0.9272 92.72%
CYP3A4 substrate - 0.5717 57.17%
CYP2C9 substrate - 0.6591 65.91%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.8433 84.33%
CYP2C9 inhibition - 0.8796 87.96%
CYP2C19 inhibition - 0.8932 89.32%
CYP2D6 inhibition - 0.9268 92.68%
CYP1A2 inhibition - 0.8604 86.04%
CYP2C8 inhibition - 0.9504 95.04%
CYP inhibitory promiscuity - 0.8407 84.07%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.6577 65.77%
Eye corrosion + 0.4745 47.45%
Eye irritation - 0.8562 85.62%
Skin irritation + 0.6887 68.87%
Skin corrosion - 0.9332 93.32%
Ames mutagenesis - 0.7764 77.64%
Human Ether-a-go-go-Related Gene inhibition + 0.7700 77.00%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6412 64.12%
skin sensitisation + 0.8621 86.21%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.9830 98.30%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.5212 52.12%
Acute Oral Toxicity (c) III 0.7872 78.72%
Estrogen receptor binding + 0.6522 65.22%
Androgen receptor binding - 0.7612 76.12%
Thyroid receptor binding + 0.5637 56.37%
Glucocorticoid receptor binding + 0.5855 58.55%
Aromatase binding + 0.5553 55.53%
PPAR gamma + 0.7576 75.76%
Honey bee toxicity - 0.7993 79.93%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9786 97.86%

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 92.74% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.86% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.25% 92.08%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 85.18% 93.10%
CHEMBL2581 P07339 Cathepsin D 82.62% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.26% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.82% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 81.15% 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.
Eucommia ulmoides

Cross-Links

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PubChem 5315119
NPASS NPC42999