4,8-Dimethyl-1,7-nonadiene

Details

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Internal ID e2ad0a89-cb12-4350-96ce-d7718cf19229
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 4,8-dimethylnona-1,7-diene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H20/c1-5-7-11(4)9-6-8-10(2)3/h5,8,11H,1,6-7,9H2,2-4H3
InChI Key WJBLCSOLILMHEZ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H20
Molecular Weight 152.28 g/mol
Exact Mass 152.156500638 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.95
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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62108-28-5
1,7-Nonadiene, 4,8-dimethyl-
DTXSID50336609
RefChem:286172
DTXCID60287698
WJBLCSOLILMHEZ-UHFFFAOYSA-N
SCHEMBL6933010
SCHEMBL7702095
DB-357741

2D Structure

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2D Structure of 4,8-Dimethyl-1,7-nonadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9844 98.44%
Caco-2 + 0.9591 95.91%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Nucleus 0.7413 74.13%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.9474 94.74%
OATP1B3 inhibitior + 0.9381 93.81%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8792 87.92%
P-glycoprotein inhibitior - 0.9848 98.48%
P-glycoprotein substrate - 0.9440 94.40%
CYP3A4 substrate - 0.6399 63.99%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9502 95.02%
CYP2C9 inhibition - 0.8962 89.62%
CYP2C19 inhibition - 0.8824 88.24%
CYP2D6 inhibition - 0.9382 93.82%
CYP1A2 inhibition - 0.7124 71.24%
CYP2C8 inhibition - 0.9917 99.17%
CYP inhibitory promiscuity - 0.7013 70.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Warning 0.5012 50.12%
Eye corrosion + 0.6793 67.93%
Eye irritation + 0.8900 89.00%
Skin irritation + 0.8727 87.27%
Skin corrosion - 0.9708 97.08%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5480 54.80%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5738 57.38%
skin sensitisation + 0.9275 92.75%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8593 85.93%
Estrogen receptor binding - 0.9756 97.56%
Androgen receptor binding - 0.9276 92.76%
Thyroid receptor binding - 0.7152 71.52%
Glucocorticoid receptor binding - 0.8410 84.10%
Aromatase binding - 0.8503 85.03%
PPAR gamma - 0.8734 87.34%
Honey bee toxicity - 0.8419 84.19%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity + 0.9913 99.13%

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
CHEMBL2581 P07339 Cathepsin D 91.39% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.62% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.66% 94.45%
CHEMBL2885 P07451 Carbonic anhydrase III 86.07% 87.45%
CHEMBL1829 O15379 Histone deacetylase 3 81.52% 95.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.02% 96.47%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.93% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.35% 99.17%

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.
Dioscorea septemloba

Cross-Links

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PubChem 534956
NPASS NPC188909