Dec-3-en-1-yne

Details

Top
Internal ID c338ec1b-fb64-4871-b779-32c7b9e6dee5
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name dec-3-en-1-yne
SMILES (Canonical) CCCCCCC=CC#C
SMILES (Isomeric) CCCCCCC=CC#C
InChI InChI=1S/C10H16/c1-3-5-7-9-10-8-6-4-2/h1,5,7H,4,6,8-10H2,2H3
InChI Key OMLUZGAUTCIZLU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.15
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
SCHEMBL17965707

2D Structure

Top
2D Structure of Dec-3-en-1-yne

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.9585 95.85%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.4237 42.37%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.8395 83.95%
OATP1B3 inhibitior + 0.9247 92.47%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9181 91.81%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9391 93.91%
CYP3A4 substrate - 0.6690 66.90%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9766 97.66%
CYP2C9 inhibition - 0.8801 88.01%
CYP2C19 inhibition - 0.9088 90.88%
CYP2D6 inhibition - 0.9441 94.41%
CYP1A2 inhibition + 0.6338 63.38%
CYP2C8 inhibition - 0.8368 83.68%
CYP inhibitory promiscuity - 0.5347 53.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.5121 51.21%
Eye corrosion + 0.9625 96.25%
Eye irritation - 0.5614 56.14%
Skin irritation + 0.8718 87.18%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5434 54.34%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5038 50.38%
skin sensitisation + 0.9585 95.85%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.9970 99.70%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8116 81.16%
Estrogen receptor binding - 0.8634 86.34%
Androgen receptor binding - 0.7449 74.49%
Thyroid receptor binding - 0.6977 69.77%
Glucocorticoid receptor binding - 0.7261 72.61%
Aromatase binding - 0.7377 73.77%
PPAR gamma - 0.6543 65.43%
Honey bee toxicity - 0.9890 98.90%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.9353 93.53%
Fish aquatic toxicity + 0.9928 99.28%

Targets

Top

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
CHEMBL230 P35354 Cyclooxygenase-2 98.42% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.59% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 94.38% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.83% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.54% 92.86%
CHEMBL2581 P07339 Cathepsin D 91.41% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.27% 91.81%
CHEMBL2039 P27338 Monoamine oxidase B 85.40% 92.51%
CHEMBL1781 P11387 DNA topoisomerase I 83.30% 97.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.89% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 82.88% 85.94%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.35% 96.00%
CHEMBL1907 P15144 Aminopeptidase N 82.33% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.86% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 81.75% 87.45%
CHEMBL3401 O75469 Pregnane X receptor 81.05% 94.73%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.02% 100.00%

Plants that contains it

Top
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.
Ficus carica

Cross-Links

Top
PubChem 137722
NPASS NPC159858