2,4,6-Octatriene, 2,6-dimethyl-, (4Z,6Z)-

Details

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Internal ID 054f51ee-9d90-435e-9a99-081a9e752a98
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (4Z,6Z)-2,6-dimethylocta-2,4,6-triene
SMILES (Canonical) CC=C(C)C=CC=C(C)C
SMILES (Isomeric) C/C=C(/C)\C=C/C=C(C)C
InChI InChI=1S/C10H16/c1-5-10(4)8-6-7-9(2)3/h5-8H,1-4H3/b8-6-,10-5-
InChI Key GQVMHMFBVWSSPF-BHJHHZOLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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(Z,Z)-Alloocimene
Allocimene, 4Z,6Z-
Alloocimene, (4Z,6Z)-
G1G39GGK9Y
UNII-G1G39GGK9Y
2,4,6-Octatriene, 2,6-dimethyl-, (4Z,6Z)-
(4Z,6Z)-alloocimene
17202-20-9
GQVMHMFBVWSSPF-BHJHHZOLSA-
2,6-dimethyl-octa-2,4cis,6cis-triene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4,6-Octatriene, 2,6-dimethyl-, (4Z,6Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.9269 92.69%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.4504 45.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8906 89.06%
OATP1B3 inhibitior + 0.9568 95.68%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7733 77.33%
P-glycoprotein inhibitior - 0.9893 98.93%
P-glycoprotein substrate - 0.9690 96.90%
CYP3A4 substrate - 0.6582 65.82%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.7944 79.44%
CYP3A4 inhibition - 0.9436 94.36%
CYP2C9 inhibition - 0.8927 89.27%
CYP2C19 inhibition - 0.9075 90.75%
CYP2D6 inhibition - 0.9281 92.81%
CYP1A2 inhibition - 0.8718 87.18%
CYP2C8 inhibition - 0.9857 98.57%
CYP inhibitory promiscuity - 0.6843 68.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6683 66.83%
Carcinogenicity (trinary) Warning 0.6100 61.00%
Eye corrosion + 0.9450 94.50%
Eye irritation + 0.9881 98.81%
Skin irritation + 0.8007 80.07%
Skin corrosion - 0.7896 78.96%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5967 59.67%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5897 58.97%
skin sensitisation + 0.8752 87.52%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.5839 58.39%
Nephrotoxicity + 0.6972 69.72%
Acute Oral Toxicity (c) III 0.8122 81.22%
Estrogen receptor binding - 0.9435 94.35%
Androgen receptor binding - 0.9663 96.63%
Thyroid receptor binding - 0.8353 83.53%
Glucocorticoid receptor binding - 0.7864 78.64%
Aromatase binding - 0.8435 84.35%
PPAR gamma - 0.8548 85.48%
Honey bee toxicity - 0.8860 88.60%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8634 86.34%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.42% 83.82%
CHEMBL2061 P19793 Retinoid X receptor alpha 81.87% 91.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.78% 96.09%
CHEMBL1870 P28702 Retinoid X receptor beta 80.08% 95.00%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 5317469
NPASS NPC254048