9-Eicosyne

Details

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Internal ID bde8e6e6-d2c7-4d1f-b7c6-7d074f0b5c3f
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Acetylenes > Alkynes > Terminal alkynes
IUPAC Name icos-9-yne
SMILES (Canonical) CCCCCCCCCCC#CCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCC#CCCCCCCCC
InChI InChI=1S/C20H38/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-17,19H2,1-2H3
InChI Key ARULVMGJDAAVBD-UHFFFAOYSA-N
Popularity 12 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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9-Icosyne
71899-38-2
icos-9-yne
9-Icosyne #
DTXSID40339568
ARULVMGJDAAVBD-UHFFFAOYSA-N

2D Structure

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2D Structure of 9-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 + 0.8793 87.93%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.5933 59.33%
OATP2B1 inhibitior - 0.8511 85.11%
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 - 0.6484 64.84%
P-glycoprotein inhibitior - 0.8749 87.49%
P-glycoprotein substrate - 0.9294 92.94%
CYP3A4 substrate - 0.7110 71.10%
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 - 0.9082 90.82%
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 + 0.9905 99.05%
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 - 0.7084 70.84%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.8711 87.11%
skin sensitisation + 0.9468 94.68%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.7118 71.18%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.7205 72.05%
Acute Oral Toxicity (c) III 0.7164 71.64%
Estrogen receptor binding - 0.6261 62.61%
Androgen receptor binding - 0.6934 69.34%
Thyroid receptor binding - 0.5602 56.02%
Glucocorticoid receptor binding - 0.8768 87.68%
Aromatase binding - 0.7107 71.07%
PPAR gamma - 0.6661 66.61%
Honey bee toxicity - 0.9823 98.23%
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 86.76% 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%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.60% 99.17%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 80.35% 85.40%

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
Portulaca oleracea

Cross-Links

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PubChem 557019
NPASS NPC255514
LOTUS LTS0129820
wikiData Q82108677