Heptadeca-1,7,9,13,15-pentaen-11-yne

Details

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Internal ID c8ff83fe-4c45-42f2-83f3-3722091a8186
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name heptadeca-1,7,9,13,15-pentaen-11-yne
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3-4,6,8,10,13,15-17H,1,5,7,9,11H2,2H3
InChI Key QXLWCTMPQRBCAQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22
Molecular Weight 226.36 g/mol
Exact Mass 226.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.10
Atomic LogP (AlogP) 4.98
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Heptadeca-1,7,9,13,15-pentaen-11-yne

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 + 0.8251 82.51%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4007 40.07%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8553 85.53%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5547 55.47%
P-glycoprotein inhibitior - 0.8931 89.31%
P-glycoprotein substrate - 0.8957 89.57%
CYP3A4 substrate - 0.5412 54.12%
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 - 0.8340 83.40%
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 + 0.7085 70.85%
Skin irritation + 0.7736 77.36%
Skin corrosion - 0.8790 87.90%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6748 67.48%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.8641 86.41%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.6482 64.82%
Acute Oral Toxicity (c) III 0.6496 64.96%
Estrogen receptor binding + 0.8689 86.89%
Androgen receptor binding - 0.6509 65.09%
Thyroid receptor binding + 0.7207 72.07%
Glucocorticoid receptor binding + 0.6324 63.24%
Aromatase binding + 0.7045 70.45%
PPAR gamma + 0.6704 67.04%
Honey bee toxicity - 0.7828 78.28%
Biodegradation - 0.7750 77.50%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.70% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.87% 99.17%
CHEMBL242 Q92731 Estrogen receptor beta 81.48% 98.35%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 81.47% 97.34%
CHEMBL2581 P07339 Cathepsin D 81.04% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 80.87% 90.17%

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.
Dahlia merckii

Cross-Links

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PubChem 162983266
LOTUS LTS0157993
wikiData Q105229697