Hexadecane

Details

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Internal ID 81827e7d-eaa2-481f-a971-506ecd0552dd
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes
IUPAC Name hexadecane
SMILES (Canonical) CCCCCCCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCCC
InChI InChI=1S/C16H34/c1-3-5-7-9-11-13-15-16-14-12-10-8-6-4-2/h3-16H2,1-2H3
InChI Key DCAYPVUWAIABOU-UHFFFAOYSA-N
Popularity 12,716 references in papers

Physical and Chemical Properties

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Molecular Formula C16H34
Molecular Weight 226.44 g/mol
Exact Mass 226.266051085 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 8.30
Atomic LogP (AlogP) 6.49
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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n-Hexadecane
544-76-3
Cetane
n-Cetane
Hexadekan
Cetan
hexadecan
Pentadecane, methyl-
Zetan
CCRIS 5833
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Hexadecane

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 + 0.9629 96.29%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5981 59.81%
OATP2B1 inhibitior - 0.8462 84.62%
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 - 0.6493 64.93%
P-glycoprotein inhibitior - 0.9287 92.87%
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 + 0.9945 99.45%
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 - 0.5926 59.26%
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 - 0.8167 81.67%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.7568 75.68%
Glucocorticoid receptor binding - 0.9110 91.10%
Aromatase binding - 0.8696 86.96%
PPAR gamma - 0.6555 65.55%
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.
Agave decipiens
Alstonia muelleriana
Angelica acutiloba
Angelica gigas
Angelica sinensis
Armoracia rusticana
Arum maculatum
Atractylodes lancea
Atractylodes macrocephala
Bellis perennis
Brassica juncea
Camptotheca acuminata
Cannabis sativa
Cirsium dipsacolepis
Cistus monspeliensis
Citrullus lanatus
Coreopsis nodosa
Cornus officinalis
Dacrydium cupressinum
Daphne odora
Digitalis purpurea
Diplotaxis harra
Dryopteris filix-mas
Elaeis guineensis
Endopappus macrocarpus subsp. macrocarpus
Etlingera elatior
Eucommia ulmoides
Glycine tomentella
Hamamelis virginiana
Helianthus tuberosus
Juglans nigra
Lantana camara
Lavandula angustifolia
Leonurus japonicus
Litchi chinensis
Malus domestica
Mandragora officinarum
Manilkara bidentata
Melia azedarach
Melissa officinalis
Mosla chinensis
Nelumbo lutea
Nicotiana undulata
Ophrys sphegodes
Panax ginseng
Panax notoginseng
Passiflora incarnata
Persea americana
Piper auritum
Piper longum
Piper nigrum
Pistacia vera
Plantago ovata
Plectranthus glabratus
Rhodiola crenulata
Rhododendron dauricum
Rosa multiflora
Rosa rugosa
Salvia fruticosa
Sauromatum venosum
Scutellaria baicalensis
Senecio cerberoanus
Senecio paludaffinis
Senegalia catechu
Seriphidium cinum
Sideritis hispida
Sideritis taurica
Tagetes erecta
Terminalia chebula
Trigonella foenum-graecum
Trigonella grandiflora
Tripolium pannonicum
Typhonium flagelliforme
Uvaria calamistrata
Vanilla madagascariensis
Vincetoxicum glaucescens
Vincetoxicum stauntonii
Vitis rotundifolia
Vitis vinifera
Xylopia sericea
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 11006
NPASS NPC154477
LOTUS LTS0134950
wikiData Q150843