5,7-Dimethylocta-1,6-diene

Details

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Internal ID 73b4dccc-8522-4eec-9d23-c10dc5130cda
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 5,7-dimethylocta-1,6-diene
SMILES (Canonical) CC(CCC=C)C=C(C)C
SMILES (Isomeric) CC(CCC=C)C=C(C)C
InChI InChI=1S/C10H18/c1-5-6-7-10(4)8-9(2)3/h5,8,10H,1,6-7H2,2-4H3
InChI Key FYZHLRMYDRUDES-UHFFFAOYSA-N
Popularity 1 reference 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 4.20
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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6874-43-7
2,4-Dimethyl 2,7-octadiene
iso-citronellene
NSC133361
1, 5,7-dimethyl-
5,7-Dimethyl-1,6-octadiene
DTXSID70299863
1,6-Octadiene, 5,7-dimethyl-
NSC-133361
FT-0694446

2D Structure

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2D Structure of 5,7-Dimethylocta-1,6-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9867 98.67%
Caco-2 + 0.8100 81.00%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Nucleus 0.8142 81.42%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.9357 93.57%
OATP1B3 inhibitior + 0.9180 91.80%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9221 92.21%
P-glycoprotein inhibitior - 0.9812 98.12%
P-glycoprotein substrate - 0.9552 95.52%
CYP3A4 substrate - 0.6465 64.65%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9679 96.79%
CYP2C9 inhibition - 0.9155 91.55%
CYP2C19 inhibition - 0.8964 89.64%
CYP2D6 inhibition - 0.9381 93.81%
CYP1A2 inhibition - 0.7714 77.14%
CYP2C8 inhibition - 0.9869 98.69%
CYP inhibitory promiscuity - 0.7429 74.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Warning 0.4987 49.87%
Eye corrosion + 0.7222 72.22%
Eye irritation + 0.8698 86.98%
Skin irritation + 0.8833 88.33%
Skin corrosion - 0.9415 94.15%
Ames mutagenesis - 0.9037 90.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6988 69.88%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5988 59.88%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5847 58.47%
Acute Oral Toxicity (c) III 0.8504 85.04%
Estrogen receptor binding - 0.9577 95.77%
Androgen receptor binding - 0.9295 92.95%
Thyroid receptor binding - 0.9179 91.79%
Glucocorticoid receptor binding - 0.8909 89.09%
Aromatase binding - 0.8782 87.82%
PPAR gamma - 0.8942 89.42%
Honey bee toxicity - 0.7220 72.20%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9750 97.50%

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 89.97% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.83% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 82.59% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.99% 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.
Artemisia capillaris

Cross-Links

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PubChem 280943
NPASS NPC79868