6-Hydroxy-2,6-dimethylocta-2,7-dienamide

Details

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Internal ID be5b4c1c-1023-469c-8dbb-60901d058731
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 6-hydroxy-2,6-dimethylocta-2,7-dienamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H17NO2/c1-4-10(3,13)7-5-6-8(2)9(11)12/h4,6,13H,1,5,7H2,2-3H3,(H2,11,12)
InChI Key ZSFBNUBMKXAEFD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H17NO2
Molecular Weight 183.25 g/mol
Exact Mass 183.125928785 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.14
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Hydroxy-2,6-dimethylocta-2,7-dienamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 + 0.5748 57.48%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.4134 41.34%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.9434 94.34%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8596 85.96%
P-glycoprotein inhibitior - 0.9833 98.33%
P-glycoprotein substrate - 0.9235 92.35%
CYP3A4 substrate - 0.5574 55.74%
CYP2C9 substrate - 0.7908 79.08%
CYP2D6 substrate - 0.8948 89.48%
CYP3A4 inhibition - 0.6638 66.38%
CYP2C9 inhibition - 0.7757 77.57%
CYP2C19 inhibition - 0.8076 80.76%
CYP2D6 inhibition - 0.9014 90.14%
CYP1A2 inhibition - 0.6285 62.85%
CYP2C8 inhibition - 0.9203 92.03%
CYP inhibitory promiscuity - 0.7125 71.25%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.5548 55.48%
Eye corrosion - 0.9719 97.19%
Eye irritation + 0.8158 81.58%
Skin irritation - 0.7232 72.32%
Skin corrosion - 0.9038 90.38%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6977 69.77%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.5424 54.24%
skin sensitisation - 0.7808 78.08%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.7107 71.07%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.4562 45.62%
Acute Oral Toxicity (c) III 0.6276 62.76%
Estrogen receptor binding - 0.8936 89.36%
Androgen receptor binding - 0.8111 81.11%
Thyroid receptor binding - 0.7644 76.44%
Glucocorticoid receptor binding - 0.5489 54.89%
Aromatase binding - 0.8743 87.43%
PPAR gamma - 0.6230 62.30%
Honey bee toxicity - 0.8823 88.23%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.5940 59.40%

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
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.46% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.75% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.52% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.15% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.72% 91.11%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 82.35% 90.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.45% 99.17%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.56% 93.65%
CHEMBL2581 P07339 Cathepsin D 80.43% 98.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85132205
LOTUS LTS0015736
wikiData Q105382477