cis-4-Decene

Details

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Internal ID cb03d509-0863-457b-9d93-097b22a017cd
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Unsaturated aliphatic hydrocarbons
IUPAC Name (Z)-dec-4-ene
SMILES (Canonical) CCCCCC=CCCC
SMILES (Isomeric) CCCCC/C=C\CCC
InChI InChI=1S/C10H20/c1-3-5-7-9-10-8-6-4-2/h7,9H,3-6,8,10H2,1-2H3/b9-7-
InChI Key SOVOPSCRHKEUNJ-CLFYSBASSA-N
Popularity 13 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20
Molecular Weight 140.27 g/mol
Exact Mass 140.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.92
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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(Z)-dec-4-ene
19398-88-0
(Z)-4-Decene
4-Decene, (Z)-
(Z)-4-C10H20
(4Z)-4-Decene #
SOVOPSCRHKEUNJ-CLFYSBASSA-N

2D Structure

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2D Structure of cis-4-Decene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9711 97.11%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.4683 46.83%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.8128 81.28%
OATP1B3 inhibitior + 0.9296 92.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8351 83.51%
P-glycoprotein inhibitior - 0.9830 98.30%
P-glycoprotein substrate - 0.9515 95.15%
CYP3A4 substrate - 0.7166 71.66%
CYP2C9 substrate - 0.8202 82.02%
CYP2D6 substrate - 0.7454 74.54%
CYP3A4 inhibition - 0.9849 98.49%
CYP2C9 inhibition - 0.9314 93.14%
CYP2C19 inhibition - 0.9425 94.25%
CYP2D6 inhibition - 0.9380 93.80%
CYP1A2 inhibition + 0.5051 50.51%
CYP2C8 inhibition - 0.9395 93.95%
CYP inhibitory promiscuity - 0.6865 68.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.5827 58.27%
Eye corrosion + 0.9822 98.22%
Eye irritation + 0.9878 98.78%
Skin irritation + 0.8759 87.59%
Skin corrosion - 0.9834 98.34%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6085 60.85%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation + 0.9753 97.53%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity - 0.9970 99.70%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5120 51.20%
Acute Oral Toxicity (c) III 0.8244 82.44%
Estrogen receptor binding - 0.9620 96.20%
Androgen receptor binding - 0.8628 86.28%
Thyroid receptor binding - 0.7837 78.37%
Glucocorticoid receptor binding - 0.8441 84.41%
Aromatase binding - 0.8973 89.73%
PPAR gamma - 0.7962 79.62%
Honey bee toxicity - 0.9850 98.50%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.6853 68.53%
Fish aquatic toxicity + 0.9908 99.08%

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 93.26% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 91.92% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.98% 99.17%
CHEMBL2581 P07339 Cathepsin D 88.69% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.61% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.22% 91.81%
CHEMBL240 Q12809 HERG 84.89% 89.76%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.31% 97.29%
CHEMBL1781 P11387 DNA topoisomerase I 83.18% 97.00%
CHEMBL1907 P15144 Aminopeptidase N 81.78% 93.31%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.24% 96.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 80.53% 85.94%

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 5364504
NPASS NPC16994