(5,6-Diformyl-1,1,4a-trimethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-yl) acetate

Details

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Internal ID 97b9f729-edd6-452c-912f-033bb383fdc6
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name (5,6-diformyl-1,1,4a-trimethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-yl) acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H24O4/c1-11(20)21-15-7-8-17(4)13(10-19)12(9-18)5-6-14(17)16(15,2)3/h5,9-10,13-15H,6-8H2,1-4H3
InChI Key LWRNXEVCYOKYID-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24O4
Molecular Weight 292.40 g/mol
Exact Mass 292.16745924 g/mol
Topological Polar Surface Area (TPSA) 60.40 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.70
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5,6-Diformyl-1,1,4a-trimethyl-2,3,4,5,8,8a-hexahydronaphthalen-2-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.7538 75.38%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8458 84.58%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.7799 77.99%
OATP1B3 inhibitior + 0.8855 88.55%
MATE1 inhibitior + 0.6000 60.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7308 73.08%
P-glycoprotein inhibitior - 0.7215 72.15%
P-glycoprotein substrate - 0.8837 88.37%
CYP3A4 substrate + 0.6439 64.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9036 90.36%
CYP3A4 inhibition - 0.6653 66.53%
CYP2C9 inhibition - 0.8664 86.64%
CYP2C19 inhibition - 0.8205 82.05%
CYP2D6 inhibition - 0.9561 95.61%
CYP1A2 inhibition - 0.9123 91.23%
CYP2C8 inhibition - 0.7077 70.77%
CYP inhibitory promiscuity - 0.8903 89.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9243 92.43%
Carcinogenicity (trinary) Non-required 0.6091 60.91%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.9708 97.08%
Skin irritation + 0.5216 52.16%
Skin corrosion - 0.9785 97.85%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6776 67.76%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.6334 63.34%
skin sensitisation + 0.5376 53.76%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6268 62.68%
Acute Oral Toxicity (c) III 0.8288 82.88%
Estrogen receptor binding + 0.7675 76.75%
Androgen receptor binding - 0.5287 52.87%
Thyroid receptor binding - 0.5856 58.56%
Glucocorticoid receptor binding - 0.6432 64.32%
Aromatase binding - 0.6631 66.31%
PPAR gamma - 0.5499 54.99%
Honey bee toxicity - 0.8351 83.51%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5355 53.55%
Fish aquatic toxicity + 1.0000 100.00%

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 96.22% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.00% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.19% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 87.44% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.15% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.87% 100.00%
CHEMBL5028 O14672 ADAM10 82.57% 97.50%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.75% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.66% 95.89%

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.
Canella winterana

Cross-Links

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PubChem 14543713
LOTUS LTS0157372
wikiData Q105158525