Heneicosane

Details

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Internal ID c523129f-55f2-4bc4-a730-87a3beb79ee0
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes
IUPAC Name henicosane
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCCC
InChI InChI=1S/C21H44/c1-3-5-7-9-11-13-15-17-19-21-20-18-16-14-12-10-8-6-4-2/h3-21H2,1-2H3
InChI Key FNAZRRHPUDJQCJ-UHFFFAOYSA-N
Popularity 794 references in papers

Physical and Chemical Properties

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Molecular Formula C21H44
Molecular Weight 296.60 g/mol
Exact Mass 296.344301404 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 11.00
Atomic LogP (AlogP) 8.44
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 18

Synonyms

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n-Heneicosane
Henicosane
629-94-7
Eicosane, methyl-
UNII-I93S5U5DMP
I93S5U5DMP
EINECS 211-118-9
AI3-36479
DTXSID9047097
CHEBI:32931
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Heneicosane

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 + 0.9023 90.23%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5981 59.81%
OATP2B1 inhibitior - 0.8491 84.91%
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 - 0.6858 68.58%
P-glycoprotein inhibitior - 0.8850 88.50%
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 + 0.9846 98.46%
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 - 0.7041 70.41%
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 - 0.7056 70.56%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.7319 73.19%
Glucocorticoid receptor binding - 0.9020 90.20%
Aromatase binding - 0.7048 70.48%
PPAR gamma - 0.6838 68.38%
Honey bee toxicity - 0.9939 99.39%
Biodegradation + 1.0000 100.00%
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.
Abies sachalinensis
Agave decipiens
Allium ampeloprasum
Aquilaria malaccensis
Aquilaria sinensis
Arabidopsis thaliana
Armoracia rusticana
Arnica montana
Artemisia annua
Aucklandia costus
Cannabis sativa
Castanopsis cuspidata
Cestrum nocturnum
Chrysanthemum indicum
Cistanche deserticola
Cistus ladanifer
Citrullus lanatus
Citrus × aurantium
Cnidium monnieri
Codonopsis pilosula
Crocus sativus
Cupressus nootkatensis
Cynomorium coccineum subsp. songaricum
Dactylanthus taylorii
Daphne odora
Digitalis purpurea
Echinacea angustifolia
Eleutherococcus giraldii
Endopappus macrocarpus subsp. macrocarpus
Ephedra sinica
Erucaria microcarpa
Foeniculum vulgare
Gossypium herbaceum
Hamamelis virginiana
Hippophae rhamnoides
Hypericum perforatum
Leuzea uniflora
Manilkara bidentata
Melissa officinalis
Morina persica
Nelumbo lutea
Nelumbo nucifera
Nepeta hindostana
Origanum vulgare
Panax ginseng
Panax notoginseng
Pelargonium endlicherianum
Persicaria bistorta
Piper nigrum
Plantago ovata
Plumeria rubra
Polygonatum odoratum
Prunus laurocerasus
Pterocarpus indicus
Rosa gallica
Rosa multiflora
Salvia fruticosa
Scutellaria baicalensis
Senna alexandrina
Sideritis hispida
Solanum stuckertii
Symphytum tuberosum
Tilia platyphyllos
Uncaria macrophylla
Vachellia rigidula
Vanilla planifolia
Vincetoxicum glaucescens
Vincetoxicum stauntonii
Vitis vinifera
Zinnia elegans

Cross-Links

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PubChem 12403
NPASS NPC223455
LOTUS LTS0039017
wikiData Q150955