Heptadecane

Details

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Internal ID aa33328e-1474-4ee2-85c3-f83ec4aae7e3
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes
IUPAC Name heptadecane
SMILES (Canonical) CCCCCCCCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCCCC
InChI InChI=1S/C17H36/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3-17H2,1-2H3
InChI Key NDJKXXJCMXVBJW-UHFFFAOYSA-N
Popularity 1,841 references in papers

Physical and Chemical Properties

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Molecular Formula C17H36
Molecular Weight 240.50 g/mol
Exact Mass 240.281701148 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 8.80
Atomic LogP (AlogP) 6.88
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

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n-Heptadecane
629-78-7
Hexadecane, methyl-
Heptadekan
EINECS 211-108-4
n-Heptadecane (d36)
UNII-H7C0J39XUM
NSC 172782
BRN 1738898
H7C0J39XUM
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Heptadecane

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 + 0.9619 96.19%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5981 59.81%
OATP2B1 inhibitior - 0.8472 84.72%
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 - 0.7047 70.47%
P-glycoprotein inhibitior - 0.9285 92.85%
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 + 0.9955 99.55%
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 - 0.6177 61.77%
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 - 0.8357 83.57%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.7063 70.63%
Glucocorticoid receptor binding - 0.9189 91.89%
Aromatase binding - 0.8514 85.14%
PPAR gamma - 0.6697 66.97%
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.
Allium ampeloprasum
Alpinia conchigera
Alstonia muelleriana
Anethum graveolens
Annona squamosa
Aristolochia debilis
Armoracia rusticana
Artemisia annua
Astilbe rubra
Atractylodes lancea
Atractylodes macrocephala
Bellis perennis
Camptotheca acuminata
Cannabis sativa
Chaenomeles sinensis
Chaenomeles speciosa
Cinnamomum verum
Cirsium dipsacolepis
Cistanche deserticola
Cistus monspeliensis
Clematis chinensis
Cnidium monnieri
Codonopsis pilosula
Combretum indicum
Coreopsis nodosa
Cornus officinalis
Cupressus nootkatensis
Cymbidium aloifolium
Cynomorium coccineum subsp. songaricum
Dacrydium cupressinum
Delphinium dictyocarpum
Dendrobium chrysanthum
Digitalis purpurea
Eclipta prostrata
Eleutherococcus giraldii
Ephedra sinica
Eucommia ulmoides
Gardenia jasminoides
Glycine tomentella
Gossypium herbaceum
Hamamelis virginiana
Helianthus tuberosus
Hordeum vulgare
Houttuynia cordata
Humulus scandens
Ladeania juncea
Lantana camara
Leonurus japonicus
Leuzea uniflora
Ligularia atroviolacea
Magnolia obovata
Magnolia officinalis
Manilkara bidentata
Melissa officinalis
Nelumbo lutea
Nelumbo nucifera
Nicotiana undulata
Ophrys sphegodes
Paederia foetida
Panax ginseng
Panax notoginseng
Passiflora incarnata
Pelargonium endlicherianum
Persicaria bistorta
Persicaria minor
Piper nigrum
Pistacia vera
Plantago ovata
Platycladus orientalis
Plumeria rubra
Prunus persica
Pyrus pyrifolia
Rosa gallica
Rosa multiflora
Ruta graveolens
Saposhnikovia divaricata
Sauromatum venosum
Scutellaria baicalensis
Scutellaria glabra
Senecio paludaffinis
Senna alexandrina
Seriphidium cinum
Solanum stuckertii
Sophora flavescens
Syringa vulgaris
Tanacetum cinerariifolium
Terminalia chebula
Trichosanthes kirilowii
Trifolium pannonicum
Trigonella grandiflora
Tripolium pannonicum
Typhonium flagelliforme
Uncaria macrophylla
Uvaria calamistrata
Vanilla planifolia
Vincetoxicum glaucescens
Vincetoxicum stauntonii
Vitis vinifera
Wurfbainia villosa

Cross-Links

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PubChem 12398
NPASS NPC239406
LOTUS LTS0038303
wikiData Q150888