Nonadecane

Details

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Internal ID cefd63cc-be8e-4895-a497-28ae23c444c8
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes
IUPAC Name nonadecane
SMILES (Canonical) CCCCCCCCCCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCC
InChI InChI=1S/C19H40/c1-3-5-7-9-11-13-15-17-19-18-16-14-12-10-8-6-4-2/h3-19H2,1-2H3
InChI Key LQERIDTXQFOHKA-UHFFFAOYSA-N
Popularity 1,004 references in papers

Physical and Chemical Properties

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Molecular Formula C19H40
Molecular Weight 268.50 g/mol
Exact Mass 268.313001276 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 9.90
Atomic LogP (AlogP) 7.66
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 16

Synonyms

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n-Nonadecane
629-92-5
Nonadekan
UNII-NMY21D3Y5T
NMY21D3Y5T
ISTD
NONADECANE, N-
EINECS 211-116-8
NSC 77136
NSC-77136
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Nonadecane

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 + 0.9309 93.09%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5981 59.81%
OATP2B1 inhibitior - 0.8480 84.80%
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 - 0.6921 69.21%
P-glycoprotein inhibitior - 0.8976 89.76%
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 + 0.9966 99.66%
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 - 0.7086 70.86%
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 - 0.7710 77.10%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.7703 77.03%
Glucocorticoid receptor binding - 0.9300 93.00%
Aromatase binding - 0.7217 72.17%
PPAR gamma - 0.6851 68.51%
Honey bee toxicity - 0.9939 99.39%
Biodegradation + 0.9250 92.50%
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.
Abies sachalinensis
Allium ampeloprasum
Armoracia rusticana
Arnica montana
Artemisia annua
Astilbe rubra
Camptotheca acuminata
Cannabis sativa
Castanopsis cuspidata
Cestrum nocturnum
Cirsium dipsacolepis
Cistanche deserticola
Cistus ladanifer
Citrullus lanatus
Clematis chinensis
Clinopodium grandiflorum
Cnidium monnieri
Codonopsis pilosula
Cornus officinalis
Cupressus nootkatensis
Cynomorium coccineum subsp. songaricum
Daphne odora
Digitalis purpurea
Diplotaxis harra
Echinacea angustifolia
Endopappus macrocarpus subsp. macrocarpus
Ephedra sinica
Festuca arundinacea
Ficus carica
Gossypium herbaceum
Hamamelis virginiana
Helianthus tuberosus
Hypericum perforatum
Lantana camara
Leonurus japonicus
Leuzea uniflora
Litchi chinensis
Lotus corniculatus subsp. corniculatus
Lycopus lucidus
Magnolia obovata
Magnolia officinalis
Manilkara bidentata
Melissa officinalis
Nelumbo lutea
Nelumbo nucifera
Panax ginseng
Paspalum scrobiculatum
Persicaria bistorta
Phyllanthus emblica
Piper nigrum
Plantago ovata
Plumeria rubra
Pogostemon cablin
Prunus laurocerasus
Prunus persica
Pyrus pyrifolia
Rosa gallica
Salvia absconditiflora
Sauromatum venosum
Scutellaria baicalensis
Serenoa repens
Sideritis hispida
Sophora flavescens
Tanacetum cinerariifolium
Trichosanthes kirilowii
Typhonium flagelliforme
Vanilla madagascariensis
Vincetoxicum glaucescens
Vincetoxicum stauntonii
Vitis vinifera
Wurfbainia villosa

Cross-Links

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PubChem 12401
NPASS NPC127122
LOTUS LTS0146180
wikiData Q150911