4-Tridecen-6-yne, (Z)-

Details

Top
Internal ID fe52f4e3-8d71-4d24-87bb-ae5bc7e6df7d
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Enynes
IUPAC Name (Z)-tridec-4-en-6-yne
SMILES (Canonical) CCCCCCC#CC=CCCC
SMILES (Isomeric) CCCCCCC#C/C=C\CCC
InChI InChI=1S/C13H22/c1-3-5-7-9-11-13-12-10-8-6-4-2/h7,9H,3-6,8,10,12H2,1-2H3/b9-7-
InChI Key NPZMKXJJWSFOQL-CLFYSBASSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H22
Molecular Weight 178.31 g/mol
Exact Mass 178.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.32
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

Top
(Z)-4-Tridecen-6-yne
(4Z)-4-Tridecen-6-yne #
NPZMKXJJWSFOQL-CLFYSBASSA-N
74744-42-6

2D Structure

Top
2D Structure of 4-Tridecen-6-yne, (Z)-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.9773 97.73%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.4685 46.85%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.8501 85.01%
OATP1B3 inhibitior + 0.9306 93.06%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8232 82.32%
P-glycoprotein inhibitior - 0.9700 97.00%
P-glycoprotein substrate - 0.8922 89.22%
CYP3A4 substrate - 0.5804 58.04%
CYP2C9 substrate - 0.6093 60.93%
CYP2D6 substrate - 0.7826 78.26%
CYP3A4 inhibition - 0.9695 96.95%
CYP2C9 inhibition - 0.8881 88.81%
CYP2C19 inhibition - 0.9147 91.47%
CYP2D6 inhibition - 0.9370 93.70%
CYP1A2 inhibition + 0.5673 56.73%
CYP2C8 inhibition - 0.8175 81.75%
CYP inhibitory promiscuity - 0.5830 58.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.5561 55.61%
Eye corrosion + 0.9423 94.23%
Eye irritation + 0.8282 82.82%
Skin irritation + 0.8131 81.31%
Skin corrosion - 0.9728 97.28%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4556 45.56%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6246 62.46%
skin sensitisation + 0.9664 96.64%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9970 99.70%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.7151 71.51%
Acute Oral Toxicity (c) III 0.8485 84.85%
Estrogen receptor binding - 0.7289 72.89%
Androgen receptor binding - 0.7018 70.18%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6324 63.24%
Aromatase binding - 0.7209 72.09%
PPAR gamma + 0.5335 53.35%
Honey bee toxicity - 0.9288 92.88%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.8918 89.18%
Fish aquatic toxicity + 0.9935 99.35%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.61% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 95.18% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 91.44% 89.63%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 90.53% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.00% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 86.06% 90.17%
CHEMBL2996 Q05655 Protein kinase C delta 85.65% 97.79%
CHEMBL2581 P07339 Cathepsin D 84.44% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 84.16% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.79% 97.29%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 83.45% 96.42%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 82.64% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.82% 96.09%

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.
Bupleurum chinense
Bupleurum falcatum
Bupleurum scorzonerifolium

Cross-Links

Top
PubChem 5367372
NPASS NPC287435