5-Eicosyne

Details

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Internal ID bb3fa4c4-c031-4d7a-b285-982ad628c809
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Acetylenes > Alkynes > Terminal alkynes
IUPAC Name icos-5-yne
SMILES (Canonical) CCCCCCCCCCCCCCC#CCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCC#CCCCC
InChI InChI=1S/C20H38/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-9,11,13-20H2,1-2H3
InChI Key ZPJDHJXVUOPHKD-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C20H38
Molecular Weight 278.50 g/mol
Exact Mass 278.297351212 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 9.90
Atomic LogP (AlogP) 7.27
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

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5-Icosyne
icos-5-yne
74685-31-7
5-Icosyne #
LZZ7Y85KYJ
CHEBI:184689
ZPJDHJXVUOPHKD-UHFFFAOYSA-N
DTXSID001318430

2D Structure

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2D Structure of 5-Eicosyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9900 99.00%
Caco-2 + 0.8309 83.09%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.5933 59.33%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9273 92.73%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5281 52.81%
P-glycoprotein inhibitior - 0.8780 87.80%
P-glycoprotein substrate - 0.9172 91.72%
CYP3A4 substrate - 0.6964 69.64%
CYP2C9 substrate - 0.8281 82.81%
CYP2D6 substrate - 0.7406 74.06%
CYP3A4 inhibition - 0.9743 97.43%
CYP2C9 inhibition - 0.8901 89.01%
CYP2C19 inhibition - 0.9305 93.05%
CYP2D6 inhibition - 0.9377 93.77%
CYP1A2 inhibition - 0.5370 53.70%
CYP2C8 inhibition - 0.8966 89.66%
CYP inhibitory promiscuity - 0.7321 73.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6027 60.27%
Eye corrosion + 0.9791 97.91%
Eye irritation + 0.9856 98.56%
Skin irritation + 0.8072 80.72%
Skin corrosion - 0.9765 97.65%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7260 72.60%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.8332 83.32%
skin sensitisation + 0.9468 94.68%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.7118 71.18%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.7095 70.95%
Acute Oral Toxicity (c) III 0.7164 71.64%
Estrogen receptor binding - 0.5939 59.39%
Androgen receptor binding - 0.6934 69.34%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.8611 86.11%
Aromatase binding - 0.7098 70.98%
PPAR gamma - 0.7326 73.26%
Honey bee toxicity - 0.9809 98.09%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.8921 89.21%
Fish aquatic toxicity + 0.9839 98.39%

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
CHEMBL230 P35354 Cyclooxygenase-2 96.46% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 94.62% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.16% 92.08%
CHEMBL2581 P07339 Cathepsin D 89.75% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 89.15% 90.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.55% 91.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.91% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 87.00% 87.45%
CHEMBL2996 Q05655 Protein kinase C delta 86.14% 97.79%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 85.40% 85.94%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.21% 97.29%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 83.49% 85.40%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.60% 99.17%

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.
Basella alba

Cross-Links

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PubChem 557014
LOTUS LTS0160747
wikiData Q105380957