5-Undecen-3-yne

Details

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Internal ID 842f2921-c614-4cd6-9042-208de0cd70a6
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (E)-undec-5-en-3-yne
SMILES (Canonical) CCCCCC=CC#CCC
SMILES (Isomeric) CCCCC/C=C/C#CCC
InChI InChI=1S/C11H18/c1-3-5-7-9-11-10-8-6-4-2/h10-11H,3-5,7,9H2,1-2H3/b11-10+
InChI Key HKGRHUQPBWLCLA-ZHACJKMWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H18
Molecular Weight 150.26 g/mol
Exact Mass 150.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.54
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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5-Undecen-3-yne, (E)-
(E)-5-Undecen-3-yne
74744-31-3
trans-5 -undecen-3-yne
(5E)-5-Undecen-3-yne
HKGRHUQPBWLCLA-ZHACJKMWSA-N

2D Structure

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2D Structure of 5-Undecen-3-yne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 + 0.9193 91.93%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4501 45.01%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.8098 80.98%
OATP1B3 inhibitior + 0.9337 93.37%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8693 86.93%
P-glycoprotein inhibitior - 0.9777 97.77%
P-glycoprotein substrate - 0.9116 91.16%
CYP3A4 substrate - 0.6145 61.45%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9646 96.46%
CYP2C9 inhibition - 0.8865 88.65%
CYP2C19 inhibition - 0.9039 90.39%
CYP2D6 inhibition - 0.9312 93.12%
CYP1A2 inhibition + 0.5631 56.31%
CYP2C8 inhibition - 0.8455 84.55%
CYP inhibitory promiscuity - 0.5565 55.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.5016 50.16%
Eye corrosion + 0.9043 90.43%
Eye irritation + 0.6963 69.63%
Skin irritation + 0.8579 85.79%
Skin corrosion - 0.9569 95.69%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6117 61.17%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5162 51.62%
skin sensitisation + 0.9680 96.80%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.9303 93.03%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5386 53.86%
Acute Oral Toxicity (c) III 0.7310 73.10%
Estrogen receptor binding - 0.9343 93.43%
Androgen receptor binding - 0.8083 80.83%
Thyroid receptor binding - 0.7768 77.68%
Glucocorticoid receptor binding - 0.7950 79.50%
Aromatase binding - 0.8526 85.26%
PPAR gamma - 0.8209 82.09%
Honey bee toxicity - 0.9378 93.78%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.6253 62.53%
Fish aquatic toxicity + 0.9845 98.45%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.82% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 93.51% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.16% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.05% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.78% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.26% 91.81%
CHEMBL221 P23219 Cyclooxygenase-1 87.04% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.70% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 82.54% 85.94%
CHEMBL1781 P11387 DNA topoisomerase I 81.08% 97.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.30% 97.25%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 5367385
NPASS NPC150738