1-(4,8-Dihydroxy-4a,8-dimethyl-1,4,5,6,7,8a-hexahydronaphthalen-2-yl)ethanone

Details

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Internal ID a9cfaeed-f1b6-4202-8172-0176cb6d59cd
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 1-(4,8-dihydroxy-4a,8-dimethyl-1,4,5,6,7,8a-hexahydronaphthalen-2-yl)ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H22O3/c1-9(15)10-7-11-13(2,12(16)8-10)5-4-6-14(11,3)17/h8,11-12,16-17H,4-7H2,1-3H3
InChI Key WRNYMVWAPLPFJG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22O3
Molecular Weight 238.32 g/mol
Exact Mass 238.15689456 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.82
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(4,8-Dihydroxy-4a,8-dimethyl-1,4,5,6,7,8a-hexahydronaphthalen-2-yl)ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6607 66.07%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7771 77.71%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.8844 88.44%
OATP1B3 inhibitior + 0.9728 97.28%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.7250 72.50%
BSEP inhibitior - 0.8422 84.22%
P-glycoprotein inhibitior - 0.9462 94.62%
P-glycoprotein substrate - 0.9087 90.87%
CYP3A4 substrate + 0.5452 54.52%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.8858 88.58%
CYP3A4 inhibition - 0.6371 63.71%
CYP2C9 inhibition - 0.8914 89.14%
CYP2C19 inhibition - 0.8964 89.64%
CYP2D6 inhibition - 0.9487 94.87%
CYP1A2 inhibition - 0.8914 89.14%
CYP2C8 inhibition - 0.9402 94.02%
CYP inhibitory promiscuity - 0.8806 88.06%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5058 50.58%
Eye corrosion - 0.9949 99.49%
Eye irritation - 0.6204 62.04%
Skin irritation + 0.6458 64.58%
Skin corrosion - 0.9672 96.72%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7372 73.72%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5904 59.04%
skin sensitisation + 0.5222 52.22%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6855 68.55%
Acute Oral Toxicity (c) III 0.7197 71.97%
Estrogen receptor binding - 0.5605 56.05%
Androgen receptor binding - 0.6040 60.40%
Thyroid receptor binding - 0.6053 60.53%
Glucocorticoid receptor binding - 0.7452 74.52%
Aromatase binding - 0.7607 76.07%
PPAR gamma - 0.8592 85.92%
Honey bee toxicity - 0.9462 94.62%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9881 98.81%

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 92.86% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.61% 82.69%
CHEMBL2581 P07339 Cathepsin D 90.10% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.78% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.97% 97.25%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.01% 85.30%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.90% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.67% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 80.19% 91.19%

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.
Teucrium heterophyllum

Cross-Links

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PubChem 162892364
LOTUS LTS0261006
wikiData Q105311434