(Z)-nonadec-3-en-1,8,10,18-tetrayne

Details

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Internal ID 879332f9-87da-4ace-8a18-a61f53b94c3b
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (Z)-nonadec-3-en-1,8,10,18-tetrayne
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H22/c1-3-5-7-9-11-13-15-17-19-18-16-14-12-10-8-6-4-2/h1-2,5,7H,6,8-14,16H2/b7-5-
InChI Key YAIWKDHSFYJROB-ALCCZGGFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H22
Molecular Weight 250.40 g/mol
Exact Mass 250.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.10
Atomic LogP (AlogP) 4.33
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-nonadec-3-en-1,8,10,18-tetrayne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9794 97.94%
Caco-2 + 0.7431 74.31%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Plasma membrane 0.3870 38.70%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.8745 87.45%
OATP1B3 inhibitior + 0.9490 94.90%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7743 77.43%
P-glycoprotein inhibitior - 0.8750 87.50%
P-glycoprotein substrate - 0.9329 93.29%
CYP3A4 substrate - 0.5747 57.47%
CYP2C9 substrate - 0.6171 61.71%
CYP2D6 substrate - 0.7542 75.42%
CYP3A4 inhibition - 0.9708 97.08%
CYP2C9 inhibition - 0.7984 79.84%
CYP2C19 inhibition - 0.8958 89.58%
CYP2D6 inhibition - 0.9624 96.24%
CYP1A2 inhibition - 0.5591 55.91%
CYP2C8 inhibition - 0.7861 78.61%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5500 55.00%
Carcinogenicity (trinary) Warning 0.4130 41.30%
Eye corrosion + 0.9782 97.82%
Eye irritation - 0.5517 55.17%
Skin irritation + 0.8467 84.67%
Skin corrosion - 0.8455 84.55%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4598 45.98%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6038 60.38%
skin sensitisation + 0.8308 83.08%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5424 54.24%
Acute Oral Toxicity (c) III 0.7874 78.74%
Estrogen receptor binding - 0.4915 49.15%
Androgen receptor binding - 0.5805 58.05%
Thyroid receptor binding + 0.5805 58.05%
Glucocorticoid receptor binding - 0.5884 58.84%
Aromatase binding - 0.5065 50.65%
PPAR gamma + 0.5885 58.85%
Honey bee toxicity - 0.9063 90.63%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.9083 90.83%

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
CHEMBL221 P23219 Cyclooxygenase-1 87.07% 90.17%
CHEMBL230 P35354 Cyclooxygenase-2 86.34% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.18% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.95% 96.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10538672
LOTUS LTS0041853
wikiData Q105345404