Heptadeca-9,16-dien-4,6-diyn-8-one

Details

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Internal ID e7d5de01-fceb-4219-afe9-3667863ca59d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name heptadeca-9,16-dien-4,6-diyn-8-one
SMILES (Canonical) CCCC#CC#CC(=O)C=CCCCCCC=C
SMILES (Isomeric) CCCC#CC#CC(=O)C=CCCCCCC=C
InChI InChI=1S/C17H22O/c1-3-5-7-9-10-12-14-16-17(18)15-13-11-8-6-4-2/h3,14,16H,1,4-7,9-10,12H2,2H3
InChI Key ZVPOCLFFKKSPRA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O
Molecular Weight 242.36 g/mol
Exact Mass 242.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 1
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 Heptadeca-9,16-dien-4,6-diyn-8-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.8251 82.51%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Plasma membrane 0.6078 60.78%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.8675 86.75%
OATP1B3 inhibitior + 0.9363 93.63%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7544 75.44%
P-glycoprotein inhibitior - 0.9105 91.05%
P-glycoprotein substrate - 0.7649 76.49%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 0.8005 80.05%
CYP2D6 substrate - 0.8632 86.32%
CYP3A4 inhibition - 0.9578 95.78%
CYP2C9 inhibition - 0.8541 85.41%
CYP2C19 inhibition - 0.8616 86.16%
CYP2D6 inhibition - 0.9558 95.58%
CYP1A2 inhibition + 0.6533 65.33%
CYP2C8 inhibition - 0.8050 80.50%
CYP inhibitory promiscuity - 0.6051 60.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.5809 58.09%
Eye corrosion + 0.9355 93.55%
Eye irritation - 0.5131 51.31%
Skin irritation + 0.6593 65.93%
Skin corrosion - 0.9286 92.86%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6517 65.17%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5322 53.22%
skin sensitisation + 0.9208 92.08%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.5520 55.20%
Acute Oral Toxicity (c) III 0.5633 56.33%
Estrogen receptor binding - 0.5702 57.02%
Androgen receptor binding - 0.5909 59.09%
Thyroid receptor binding + 0.5378 53.78%
Glucocorticoid receptor binding - 0.5340 53.40%
Aromatase binding - 0.6082 60.82%
PPAR gamma + 0.6326 63.26%
Honey bee toxicity - 0.9090 90.90%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6211 62.11%
Fish aquatic toxicity + 0.9632 96.32%

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 94.62% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 94.57% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.13% 99.17%
CHEMBL2581 P07339 Cathepsin D 93.39% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.49% 89.34%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.92% 94.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.26% 92.08%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 80.00% 85.40%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 80.00% 98.51%

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.
Erodiophyllum elderi

Cross-Links

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PubChem 163052100
LOTUS LTS0275283
wikiData Q105384506