1-Nonene

Details

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Internal ID 91c89904-4dfa-4432-95f6-c7cde8c4217e
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Unsaturated aliphatic hydrocarbons
IUPAC Name non-1-ene
SMILES (Canonical) CCCCCCCC=C
SMILES (Isomeric) CCCCCCCC=C
InChI InChI=1S/C9H18/c1-3-5-7-9-8-6-4-2/h3H,1,4-9H2,2H3
InChI Key JRZJOMJEPLMPRA-UHFFFAOYSA-N
Popularity 712 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 5.20
Atomic LogP (AlogP) 3.53
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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124-11-8
non-1-ene
n-Non-1-ene
NONYLENE
alpha-Nonene
Propylene trimer
NONENE
Nonene, 1-
Nonene-(1)
1-N-None
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Nonene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.9608 96.08%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4578 45.78%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9249 92.49%
OATP1B3 inhibitior + 0.9239 92.39%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9407 94.07%
P-glycoprotein inhibitior - 0.9880 98.80%
P-glycoprotein substrate - 0.9510 95.10%
CYP3A4 substrate - 0.6997 69.97%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9832 98.32%
CYP2C9 inhibition - 0.9157 91.57%
CYP2C19 inhibition - 0.9190 91.90%
CYP2D6 inhibition - 0.9426 94.26%
CYP1A2 inhibition + 0.5418 54.18%
CYP2C8 inhibition - 0.8997 89.97%
CYP inhibitory promiscuity - 0.6838 68.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.5494 54.94%
Eye corrosion + 0.9841 98.41%
Eye irritation + 0.9943 99.43%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.9742 97.42%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5916 59.16%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5475 54.75%
skin sensitisation + 0.9605 96.05%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6384 63.84%
Acute Oral Toxicity (c) III 0.6572 65.72%
Estrogen receptor binding - 0.9418 94.18%
Androgen receptor binding - 0.8774 87.74%
Thyroid receptor binding - 0.8038 80.38%
Glucocorticoid receptor binding - 0.8001 80.01%
Aromatase binding - 0.8648 86.48%
PPAR gamma - 0.8720 87.20%
Honey bee toxicity - 0.9654 96.54%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.8700 87.00%
Fish aquatic toxicity + 0.9955 99.55%

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 95.47% 92.08%
CHEMBL240 Q12809 HERG 95.26% 89.76%
CHEMBL230 P35354 Cyclooxygenase-2 91.40% 89.63%
CHEMBL2581 P07339 Cathepsin D 90.78% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.99% 92.86%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.54% 85.94%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 89.21% 85.40%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.06% 97.29%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.64% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.37% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 87.83% 87.45%
CHEMBL221 P23219 Cyclooxygenase-1 86.18% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.65% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.98% 89.34%
CHEMBL2996 Q05655 Protein kinase C delta 80.95% 97.79%
CHEMBL1907 P15144 Aminopeptidase N 80.71% 93.31%

Cross-Links

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PubChem 31285
NPASS NPC69750
LOTUS LTS0022235
wikiData Q15687205