(E,3S)-icos-4-en-1,14,19-triyn-3-ol

Details

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Internal ID c61b57b9-f4fb-4572-82fc-1793213fcd7c
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (E,3S)-icos-4-en-1,14,19-triyn-3-ol
SMILES (Canonical) C#CCCCC#CCCCCCCCCC=CC(C#C)O
SMILES (Isomeric) C#CCCCC#CCCCCCCCC/C=C/[C@@H](C#C)O
InChI InChI=1S/C20H28O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)4-2/h1-2,18-21H,5-7,10-17H2/b19-18+/t20-/m1/s1
InChI Key HKCQWELWYDDSMN-LNEUUDGLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O
Molecular Weight 284.40 g/mol
Exact Mass 284.214015512 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 6.00
Atomic LogP (AlogP) 4.46
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E,3S)-icos-4-en-1,14,19-triyn-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9694 96.94%
Caco-2 + 0.6537 65.37%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.4289 42.89%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.8719 87.19%
OATP1B3 inhibitior + 0.9472 94.72%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5478 54.78%
P-glycoprotein inhibitior - 0.8295 82.95%
P-glycoprotein substrate - 0.9404 94.04%
CYP3A4 substrate - 0.5771 57.71%
CYP2C9 substrate - 0.8005 80.05%
CYP2D6 substrate - 0.7059 70.59%
CYP3A4 inhibition - 0.9388 93.88%
CYP2C9 inhibition - 0.7612 76.12%
CYP2C19 inhibition - 0.8492 84.92%
CYP2D6 inhibition - 0.9538 95.38%
CYP1A2 inhibition - 0.5178 51.78%
CYP2C8 inhibition - 0.8543 85.43%
CYP inhibitory promiscuity - 0.5963 59.63%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.4994 49.94%
Eye corrosion + 0.9501 95.01%
Eye irritation - 0.7687 76.87%
Skin irritation + 0.7771 77.71%
Skin corrosion - 0.5000 50.00%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3947 39.47%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5446 54.46%
skin sensitisation + 0.8174 81.74%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.6658 66.58%
Acute Oral Toxicity (c) III 0.3283 32.83%
Estrogen receptor binding - 0.4754 47.54%
Androgen receptor binding - 0.8158 81.58%
Thyroid receptor binding + 0.6903 69.03%
Glucocorticoid receptor binding - 0.6402 64.02%
Aromatase binding - 0.5140 51.40%
PPAR gamma + 0.7228 72.28%
Honey bee toxicity - 0.8521 85.21%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.6478 64.78%

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
CHEMBL221 P23219 Cyclooxygenase-1 93.58% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.29% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.32% 99.17%
CHEMBL2581 P07339 Cathepsin D 87.87% 98.95%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 87.54% 92.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.50% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.44% 95.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.11% 97.21%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162817405
LOTUS LTS0024587
wikiData Q105029585