Z-5-Nonadecene

Details

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Internal ID 9cb187d2-3d02-4092-8b32-4179820ccd01
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Unsaturated aliphatic hydrocarbons
IUPAC Name (Z)-nonadec-5-ene
SMILES (Canonical) CCCCCCCCCCCCCC=CCCCC
SMILES (Isomeric) CCCCCCCCCCCCC/C=C\CCCC
InChI InChI=1S/C19H38/c1-3-5-7-9-11-13-15-17-19-18-16-14-12-10-8-6-4-2/h9,11H,3-8,10,12-19H2,1-2H3/b11-9-
InChI Key LHPVEDYVSCTZAY-LUAWRHEFSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C19H38
Molecular Weight 266.50 g/mol
Exact Mass 266.297351212 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 9.60
Atomic LogP (AlogP) 7.43
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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(Z)-5-Nonadecene
(5Z)-5-Nonadecene #
LHPVEDYVSCTZAY-LUAWRHEFSA-N

2D Structure

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2D Structure of Z-5-Nonadecene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9047 90.47%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4683 46.83%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.8491 84.91%
OATP1B3 inhibitior + 0.9296 92.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4684 46.84%
P-glycoprotein inhibitior - 0.8795 87.95%
P-glycoprotein substrate - 0.9531 95.31%
CYP3A4 substrate - 0.7154 71.54%
CYP2C9 substrate - 0.8202 82.02%
CYP2D6 substrate - 0.7454 74.54%
CYP3A4 inhibition - 0.9849 98.49%
CYP2C9 inhibition - 0.9314 93.14%
CYP2C19 inhibition - 0.9425 94.25%
CYP2D6 inhibition - 0.9380 93.80%
CYP1A2 inhibition + 0.5051 50.51%
CYP2C8 inhibition - 0.9398 93.98%
CYP inhibitory promiscuity - 0.6865 68.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.5827 58.27%
Eye corrosion + 0.9822 98.22%
Eye irritation + 0.9807 98.07%
Skin irritation + 0.8759 87.59%
Skin corrosion - 0.9834 98.34%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4649 46.49%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5184 51.84%
skin sensitisation + 0.9753 97.53%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9970 99.70%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5389 53.89%
Acute Oral Toxicity (c) III 0.8244 82.44%
Estrogen receptor binding - 0.7368 73.68%
Androgen receptor binding - 0.7621 76.21%
Thyroid receptor binding + 0.6137 61.37%
Glucocorticoid receptor binding - 0.8122 81.22%
Aromatase binding - 0.6630 66.30%
PPAR gamma + 0.6957 69.57%
Honey bee toxicity - 0.9889 98.89%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity + 0.9153 91.53%
Fish aquatic toxicity + 0.9908 99.08%

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 96.10% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 95.27% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.32% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.55% 92.86%
CHEMBL2581 P07339 Cathepsin D 91.25% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.29% 97.29%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.77% 91.81%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.15% 85.94%
CHEMBL2885 P07451 Carbonic anhydrase III 84.92% 87.45%
CHEMBL1781 P11387 DNA topoisomerase I 84.48% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.10% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 81.78% 93.31%
CHEMBL2996 Q05655 Protein kinase C delta 81.72% 97.79%
CHEMBL221 P23219 Cyclooxygenase-1 80.59% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.07% 96.95%

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.
Ammodaucus leucotrichus
Cornus officinalis

Cross-Links

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PubChem 5364560
NPASS NPC71323
LOTUS LTS0027884
wikiData Q105151893