trans-3-Nonene

Details

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Internal ID 8cc493a9-2912-4d6a-806e-80cc14e6b2f6
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Unsaturated aliphatic hydrocarbons
IUPAC Name (E)-non-3-ene
SMILES (Canonical) CCCCCC=CCC
SMILES (Isomeric) CCCCC/C=C/CC
InChI InChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h5,7H,3-4,6,8-9H2,1-2H3/b7-5+
InChI Key YCBSHDKATAPNIA-FNORWQNLSA-N
Popularity 30 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18
Molecular Weight 126.24 g/mol
Exact Mass 126.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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(E)-Non-3-ene
20063-92-7
3-Nonene, (E)-
3-Nonene, (3E)-
(E)-3-Nonene
UNII-697F6717WI
EINECS 243-495-0
697F6717WI
20063-77-8
1-Heptene, ethyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of trans-3-Nonene

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 + 0.9761 97.61%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.4683 46.83%
OATP2B1 inhibitior - 0.8491 84.91%
OATP1B1 inhibitior + 0.8018 80.18%
OATP1B3 inhibitior + 0.9296 92.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8973 89.73%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.9425 94.25%
CYP3A4 substrate - 0.7100 71.00%
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 - 0.9399 93.99%
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 + 0.9798 97.98%
Skin irritation + 0.8759 87.59%
Skin corrosion - 0.9834 98.34%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5931 59.31%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.9753 97.53%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.9970 99.70%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.5957 59.57%
Acute Oral Toxicity (c) III 0.8244 82.44%
Estrogen receptor binding - 0.9389 93.89%
Androgen receptor binding - 0.8494 84.94%
Thyroid receptor binding - 0.8115 81.15%
Glucocorticoid receptor binding - 0.8338 83.38%
Aromatase binding - 0.9044 90.44%
PPAR gamma - 0.7630 76.30%
Honey bee toxicity - 0.9864 98.64%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.7153 71.53%
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 92.04% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.68% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.35% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.41% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.22% 91.81%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.07% 97.29%
CHEMBL1781 P11387 DNA topoisomerase I 83.18% 97.00%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 82.33% 85.94%
CHEMBL1907 P15144 Aminopeptidase N 81.78% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.94% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 80.91% 87.45%

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.
Oplopanax elatus

Cross-Links

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PubChem 5364445
NPASS NPC229698