cis-2,6-Dimethyl-2,6-octadiene

Details

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Internal ID 195450f2-3363-4ab6-a0e3-b7ab92f48d45
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (6Z)-2,6-dimethylocta-2,6-diene
SMILES (Canonical) CC=C(C)CCC=C(C)C
SMILES (Isomeric) C/C=C(/C)\CCC=C(C)C
InChI InChI=1S/C10H18/c1-5-10(4)8-6-7-9(2)3/h5,7H,6,8H2,1-4H3/b10-5-
InChI Key MZPDTOMKQCMETI-YHYXMXQVSA-N
Popularity 10 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 4.10
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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2492-22-0
(6Z)-2,6-dimethylocta-2,6-diene
2,6-Dimethyl-2-trans-6-octadiene
(6Z)-2,6-Dimethyl-2,6-octadiene
MZPDTOMKQCMETI-YHYXMXQVSA-N
2,6-dimethyl-octa-2,6cis-diene
DTXSID001015872
(z)-2,6-dimethyl-2,6-octadiene
(Z)-2,6-dimethylocta-2,6-diene
trans-2,6-Dimethyl-2,6-octadiene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of cis-2,6-Dimethyl-2,6-octadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.8888 88.88%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Nucleus 0.8412 84.12%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.9207 92.07%
OATP1B3 inhibitior + 0.9203 92.03%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7548 75.48%
P-glycoprotein inhibitior - 0.9870 98.70%
P-glycoprotein substrate - 0.9780 97.80%
CYP3A4 substrate - 0.7104 71.04%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9778 97.78%
CYP2C9 inhibition - 0.9299 92.99%
CYP2C19 inhibition - 0.9233 92.33%
CYP2D6 inhibition - 0.9388 93.88%
CYP1A2 inhibition - 0.7903 79.03%
CYP2C8 inhibition - 0.9867 98.67%
CYP inhibitory promiscuity - 0.7109 71.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Warning 0.4845 48.45%
Eye corrosion + 0.6931 69.31%
Eye irritation + 0.9185 91.85%
Skin irritation + 0.9149 91.49%
Skin corrosion - 0.8551 85.51%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6288 62.88%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.9497 94.97%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.6434 64.34%
Acute Oral Toxicity (c) III 0.8808 88.08%
Estrogen receptor binding - 0.9704 97.04%
Androgen receptor binding - 0.9006 90.06%
Thyroid receptor binding - 0.9017 90.17%
Glucocorticoid receptor binding - 0.8764 87.64%
Aromatase binding - 0.8852 88.52%
PPAR gamma - 0.8632 86.32%
Honey bee toxicity - 0.9220 92.20%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9451 94.51%

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 92.62% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.44% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.93% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 81.29% 94.73%
CHEMBL2581 P07339 Cathepsin D 81.20% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 80.59% 90.17%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.05% 93.10%

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.
Citrus × aurantium

Cross-Links

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PubChem 5352478
NPASS NPC173914