(6E)-8-oxogeraniol

Details

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Internal ID a7120bd1-f30e-4f98-b378-3b157ec9b4bd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (2E,6E)-8-hydroxy-2,6-dimethylocta-2,6-dienal
SMILES (Canonical) CC(=CCO)CCC=C(C)C=O
SMILES (Isomeric) C/C(=C\CO)/CC/C=C(\C)/C=O
InChI InChI=1S/C10H16O2/c1-9(6-7-11)4-3-5-10(2)8-12/h5-6,8,11H,3-4,7H2,1-2H3/b9-6+,10-5+
InChI Key FRKZCCBKUZTFCA-TXFIJWAUSA-N
Popularity 31 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O2
Molecular Weight 168.23 g/mol
Exact Mass 168.115029749 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.85
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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(2E,6E)-8-hydroxy-2,6-dimethylocta-2,6-dienal
CHEBI:64236
RefChem:1050681
38290-51-6
10-oxogeraniol
2,6-Dimethyl-8-hydroxy-2E,6E-octadienal
2,6-Octadienal, 8-hydroxy-2,6-dimethyl-, (2E,6E)-
starbld0001411
(2E,6E)-8-Hydroxy-2,6-dimethyl-2,6-octadienal
SCHEMBL1300611
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (6E)-8-oxogeraniol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 + 0.8822 88.22%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4639 46.39%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.9237 92.37%
OATP1B3 inhibitior + 0.9196 91.96%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8793 87.93%
P-glycoprotein inhibitior - 0.9860 98.60%
P-glycoprotein substrate - 0.9506 95.06%
CYP3A4 substrate - 0.6053 60.53%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate - 0.8429 84.29%
CYP3A4 inhibition - 0.9189 91.89%
CYP2C9 inhibition - 0.8926 89.26%
CYP2C19 inhibition - 0.9132 91.32%
CYP2D6 inhibition - 0.8957 89.57%
CYP1A2 inhibition - 0.7373 73.73%
CYP2C8 inhibition - 0.9747 97.47%
CYP inhibitory promiscuity - 0.8422 84.22%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6839 68.39%
Eye corrosion + 0.6985 69.85%
Eye irritation + 0.8779 87.79%
Skin irritation + 0.5790 57.90%
Skin corrosion - 0.9667 96.67%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5912 59.12%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation + 0.8414 84.14%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.8923 89.23%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6103 61.03%
Acute Oral Toxicity (c) III 0.8094 80.94%
Estrogen receptor binding - 0.9750 97.50%
Androgen receptor binding - 0.8939 89.39%
Thyroid receptor binding - 0.8917 89.17%
Glucocorticoid receptor binding - 0.8323 83.23%
Aromatase binding - 0.8337 83.37%
PPAR gamma - 0.7780 77.80%
Honey bee toxicity - 0.9439 94.39%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9432 94.32%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.47% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.50% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.56% 98.95%
CHEMBL2664 P23526 Adenosylhomocysteinase 81.94% 86.67%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.54% 93.00%

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.
Lanxangia tsaoko
Rauvolfia serpentina

Cross-Links

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PubChem 11412603
NPASS NPC111879
LOTUS LTS0040114
wikiData Q27133145