3,7-Dimethyl-9-(2,6,6-trimethylcyclohex-2-en-1-yl)nona-2,6-dien-1-ol

Details

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Internal ID 1a712990-dd4c-44d5-ad2a-60e3eed241d1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Retinoids
IUPAC Name 3,7-dimethyl-9-(2,6,6-trimethylcyclohex-2-en-1-yl)nona-2,6-dien-1-ol
SMILES (Canonical) CC1=CCCC(C1CCC(=CCCC(=CCO)C)C)(C)C
SMILES (Isomeric) CC1=CCCC(C1CCC(=CCCC(=CCO)C)C)(C)C
InChI InChI=1S/C20H34O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h8,10,13,19,21H,6-7,9,11-12,14-15H2,1-5H3
InChI Key WJFFOVVCZPLQQN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H34O
Molecular Weight 290.50 g/mol
Exact Mass 290.260965704 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.81
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7-Dimethyl-9-(2,6,6-trimethylcyclohex-2-en-1-yl)nona-2,6-dien-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 + 0.7655 76.55%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.7524 75.24%
OATP2B1 inhibitior - 0.8526 85.26%
OATP1B1 inhibitior + 0.8945 89.45%
OATP1B3 inhibitior - 0.3227 32.27%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.7906 79.06%
P-glycoprotein inhibitior - 0.8034 80.34%
P-glycoprotein substrate - 0.7471 74.71%
CYP3A4 substrate + 0.5640 56.40%
CYP2C9 substrate - 0.7919 79.19%
CYP2D6 substrate - 0.7754 77.54%
CYP3A4 inhibition - 0.7562 75.62%
CYP2C9 inhibition - 0.8345 83.45%
CYP2C19 inhibition - 0.8598 85.98%
CYP2D6 inhibition - 0.9067 90.67%
CYP1A2 inhibition - 0.8817 88.17%
CYP2C8 inhibition - 0.5631 56.31%
CYP inhibitory promiscuity - 0.6333 63.33%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7928 79.28%
Carcinogenicity (trinary) Non-required 0.6231 62.31%
Eye corrosion - 0.8956 89.56%
Eye irritation - 0.8642 86.42%
Skin irritation + 0.5637 56.37%
Skin corrosion - 0.9733 97.33%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6755 67.55%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation + 0.8008 80.08%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7797 77.97%
Estrogen receptor binding - 0.6265 62.65%
Androgen receptor binding - 0.7707 77.07%
Thyroid receptor binding + 0.5879 58.79%
Glucocorticoid receptor binding + 0.5422 54.22%
Aromatase binding - 0.5940 59.40%
PPAR gamma + 0.7030 70.30%
Honey bee toxicity - 0.9101 91.01%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9885 98.85%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.02% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.02% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.52% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 86.54% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.44% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.65% 100.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.04% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.77% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.46% 95.56%

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 74051292
LOTUS LTS0089322
wikiData Q105306742