(7Z,9E)-heptadeca-1,7,9-trien-11,13,15-triyne

Details

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Internal ID 8c05129c-15be-413b-b7b1-15af6394360c
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (7Z,9E)-heptadeca-1,7,9-trien-11,13,15-triyne
SMILES (Canonical) CC#CC#CC#CC=CC=CCCCCC=C
SMILES (Isomeric) CC#CC#CC#C/C=C/C=C\CCCCC=C
InChI InChI=1S/C17H18/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3,13,15-17H,1,5,7,9,11H2,2H3/b15-13-,17-16+
InChI Key LEQCZKIMKYGCIQ-OBJKYRPYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18
Molecular Weight 222.32 g/mol
Exact Mass 222.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (7Z,9E)-heptadeca-1,7,9-trien-11,13,15-triyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9775 97.75%
Caco-2 + 0.8332 83.32%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.4007 40.07%
OATP2B1 inhibitior - 0.8618 86.18%
OATP1B1 inhibitior + 0.8604 86.04%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8677 86.77%
P-glycoprotein inhibitior - 0.9293 92.93%
P-glycoprotein substrate - 0.8667 86.67%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9215 92.15%
CYP2C9 inhibition - 0.8443 84.43%
CYP2C19 inhibition - 0.8716 87.16%
CYP2D6 inhibition - 0.9563 95.63%
CYP1A2 inhibition - 0.6012 60.12%
CYP2C8 inhibition - 0.8458 84.58%
CYP inhibitory promiscuity - 0.5757 57.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.4043 40.43%
Eye corrosion + 0.9782 97.82%
Eye irritation + 0.5563 55.63%
Skin irritation + 0.7736 77.36%
Skin corrosion - 0.8790 87.90%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4372 43.72%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation + 0.8641 86.41%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7364 73.64%
Acute Oral Toxicity (c) III 0.6496 64.96%
Estrogen receptor binding - 0.6483 64.83%
Androgen receptor binding - 0.5436 54.36%
Thyroid receptor binding + 0.5185 51.85%
Glucocorticoid receptor binding - 0.6910 69.10%
Aromatase binding + 0.5295 52.95%
PPAR gamma + 0.5720 57.20%
Honey bee toxicity - 0.7830 78.30%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9200 92.00%

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
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 86.87% 96.42%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.39% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.83% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 83.64% 90.17%
CHEMBL2581 P07339 Cathepsin D 83.13% 98.95%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 82.62% 97.34%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.43% 89.34%
CHEMBL242 Q92731 Estrogen receptor beta 80.61% 98.35%

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.
Artemisia argyi
Mangifera indica

Cross-Links

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PubChem 5318013
NPASS NPC266859