Eicosane

Details

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Internal ID c83de9f7-fa96-402f-a275-1f47e7f8a761
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes
IUPAC Name icosane
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCC
InChI InChI=1S/C20H42/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3
InChI Key CBFCDTFDPHXCNY-UHFFFAOYSA-N
Popularity 2,034 references in papers

Physical and Chemical Properties

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Molecular Formula C20H42
Molecular Weight 282.50 g/mol
Exact Mass 282.328651340 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 10.40
Atomic LogP (AlogP) 8.05
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 17

Synonyms

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n-Eicosane
Icosane
112-95-8
n-icosane
Nonadecane, methyl-
CCRIS 663
octyldodecane
UNII-3AYA9KEC48
EINECS 204-018-1
3AYA9KEC48
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Eicosane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.9197 91.97%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5981 59.81%
OATP2B1 inhibitior - 0.8487 84.87%
OATP1B1 inhibitior + 0.9552 95.52%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6474 64.74%
P-glycoprotein inhibitior - 0.8975 89.75%
P-glycoprotein substrate - 0.9516 95.16%
CYP3A4 substrate - 0.7947 79.47%
CYP2C9 substrate - 0.8415 84.15%
CYP2D6 substrate - 0.7215 72.15%
CYP3A4 inhibition - 0.9877 98.77%
CYP2C9 inhibition - 0.9349 93.49%
CYP2C19 inhibition - 0.9540 95.40%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.6175 61.75%
CYP2C8 inhibition - 0.9765 97.65%
CYP inhibitory promiscuity - 0.8149 81.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6328 63.28%
Eye corrosion + 0.9946 99.46%
Eye irritation + 0.9952 99.52%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.9874 98.74%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7566 75.66%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.8836 88.36%
skin sensitisation + 0.9563 95.63%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity - 0.6948 69.48%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6552 65.52%
Acute Oral Toxicity (c) III 0.6143 61.43%
Estrogen receptor binding - 0.7180 71.80%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.7475 74.75%
Glucocorticoid receptor binding - 0.9065 90.65%
Aromatase binding - 0.7032 70.32%
PPAR gamma - 0.7231 72.31%
Honey bee toxicity - 0.9939 99.39%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity + 0.8690 86.90%
Fish aquatic toxicity + 0.9770 97.70%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.23% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.92% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 91.78% 89.63%
CHEMBL2581 P07339 Cathepsin D 89.44% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.64% 91.81%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.59% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.93% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 86.52% 87.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.15% 85.94%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 83.58% 90.24%
CHEMBL2996 Q05655 Protein kinase C delta 83.44% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.77% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 81.78% 93.31%

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.
Ageratum conyzoides
Alstonia muelleriana
Annona squamosa
Aquilaria malaccensis
Aquilaria sinensis
Arabidopsis thaliana
Armoracia rusticana
Arnica montana
Artemisia annua
Azadirachta indica
Cannabis sativa
Carthamus oxyacantha
Castanopsis cuspidata
Cestrum nocturnum
Cirsium dipsacolepis
Cistus ladanifer
Citrus × aurantium
Citrus medica
Clusia spiritu-sanctensis
Coreopsis nodosa
Coriandrum sativum
Cynomorium coccineum subsp. songaricum
Dacrydium cupressinum
Digitalis purpurea
Diplotaxis harra
Echinacea angustifolia
Glycine tomentella
Hamamelis virginiana
Hansenia forbesii
Hansenia weberbaueriana
Helianthus tuberosus
Hyssopus officinalis
Leuzea uniflora
Litchi chinensis
Magnolia obovata
Magnolia officinalis
Mandragora officinarum
Manilkara bidentata
Melicope lunu-ankenda
Melissa officinalis
Mentha spicata
Mikania monagasensis
Nelumbo lutea
Nelumbo nucifera
Nepeta hindostana
Nicotiana undulata
Passiflora incarnata
Persicaria bistorta
Persicaria minor
Piper nigrum
Plantago ovata
Polygonatum odoratum
Prunus laurocerasus
Rehmannia glutinosa
Rosa centifolia
Rosa multiflora
Salvia aethiopis
Salvia fruticosa
Scutellaria baicalensis
Senecio paludaffinis
Senna alexandrina
Seriphidium cinum
Sideritis taurica
Solanum stuckertii
Taraxacum coreanum
Taraxacum mongolicum
Taraxacum officinale
Taraxacum platycarpum
Taraxacum sinicum
Trigonella grandiflora
Tripolium pannonicum
Typhonium flagelliforme
Uvaria calamistrata
Vaccinium corymbosum
Vanilla madagascariensis
Vincetoxicum glaucescens
Vincetoxicum stauntonii
Vitis vinifera

Cross-Links

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PubChem 8222
NPASS NPC96218
LOTUS LTS0125771
wikiData Q105128602