4-Decyne

Details

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Internal ID 23a6a9c9-6c02-421d-bf36-024e667bbff6
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Acetylenes > Alkynes > Terminal alkynes
IUPAC Name dec-4-yne
SMILES (Canonical) CCCCCC#CCCC
SMILES (Isomeric) CCCCCC#CCCC
InChI InChI=1S/C10H18/c1-3-5-7-9-10-8-6-4-2/h3-7,9H2,1-2H3
InChI Key KVUNBQMRRNMQIZ-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18
Molecular Weight 138.25 g/mol
Exact Mass 138.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.37
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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2384-86-3
dec-4-yne
4-C10H18
ACIDBLACK52
?4-DECYNE
DTXSID30178544
KVUNBQMRRNMQIZ-UHFFFAOYSA-N
CAA38486
MFCD00039978
AKOS006228976
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Decyne

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9900 99.00%
Caco-2 + 0.9592 95.92%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.5933 59.33%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.9247 92.47%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8863 88.63%
P-glycoprotein inhibitior - 0.9803 98.03%
P-glycoprotein substrate - 0.8980 89.80%
CYP3A4 substrate - 0.6880 68.80%
CYP2C9 substrate - 0.8281 82.81%
CYP2D6 substrate - 0.7406 74.06%
CYP3A4 inhibition - 0.9743 97.43%
CYP2C9 inhibition - 0.8901 89.01%
CYP2C19 inhibition - 0.9305 93.05%
CYP2D6 inhibition - 0.9377 93.77%
CYP1A2 inhibition - 0.5370 53.70%
CYP2C8 inhibition - 0.9381 93.81%
CYP inhibitory promiscuity - 0.7321 73.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6027 60.27%
Eye corrosion + 0.9791 97.91%
Eye irritation + 0.9967 99.67%
Skin irritation + 0.8072 80.72%
Skin corrosion - 0.9765 97.65%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7382 73.82%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7402 74.02%
skin sensitisation + 0.9468 94.68%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.7118 71.18%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.7312 73.12%
Acute Oral Toxicity (c) III 0.7164 71.64%
Estrogen receptor binding - 0.8921 89.21%
Androgen receptor binding - 0.7773 77.73%
Thyroid receptor binding - 0.7142 71.42%
Glucocorticoid receptor binding - 0.9028 90.28%
Aromatase binding - 0.8592 85.92%
PPAR gamma - 0.8112 81.12%
Honey bee toxicity - 0.9783 97.83%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.5834 58.34%
Fish aquatic toxicity + 0.9839 98.39%

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
CHEMBL230 P35354 Cyclooxygenase-2 96.55% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.02% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.49% 92.08%
CHEMBL2581 P07339 Cathepsin D 90.45% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.26% 91.81%
CHEMBL221 P23219 Cyclooxygenase-1 88.67% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.44% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 84.47% 97.79%
CHEMBL1907 P15144 Aminopeptidase N 84.13% 93.31%
CHEMBL2885 P07451 Carbonic anhydrase III 82.93% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.14% 99.17%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.48% 85.94%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.52% 97.29%

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.
Diplotaenia cachrydifolia

Cross-Links

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PubChem 16944
LOTUS LTS0146859
wikiData Q72461786