(1-Hydroxy-8-methyl-6-oxo-2-propan-2-yl-1,2,3,4,5,8a-hexahydronaphthalen-4a-yl)methyl acetate

Details

Top
Internal ID 9a949fa2-2c2d-4295-8243-cc620e6bd832
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (1-hydroxy-8-methyl-6-oxo-2-propan-2-yl-1,2,3,4,5,8a-hexahydronaphthalen-4a-yl)methyl acetate
SMILES (Canonical) CC1=CC(=O)CC2(C1C(C(CC2)C(C)C)O)COC(=O)C
SMILES (Isomeric) CC1=CC(=O)CC2(C1C(C(CC2)C(C)C)O)COC(=O)C
InChI InChI=1S/C17H26O4/c1-10(2)14-5-6-17(9-21-12(4)18)8-13(19)7-11(3)15(17)16(14)20/h7,10,14-16,20H,5-6,8-9H2,1-4H3
InChI Key PWOKMCFWNPPAQN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H26O4
Molecular Weight 294.40 g/mol
Exact Mass 294.18310931 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.70
Atomic LogP (AlogP) 2.50
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (1-Hydroxy-8-methyl-6-oxo-2-propan-2-yl-1,2,3,4,5,8a-hexahydronaphthalen-4a-yl)methyl acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 + 0.6320 63.20%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.9342 93.42%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.9151 91.51%
OATP1B3 inhibitior + 0.8623 86.23%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.6026 60.26%
BSEP inhibitior + 0.6086 60.86%
P-glycoprotein inhibitior - 0.7573 75.73%
P-glycoprotein substrate - 0.6492 64.92%
CYP3A4 substrate + 0.5937 59.37%
CYP2C9 substrate - 0.7735 77.35%
CYP2D6 substrate - 0.9017 90.17%
CYP3A4 inhibition - 0.8003 80.03%
CYP2C9 inhibition - 0.7078 70.78%
CYP2C19 inhibition - 0.8337 83.37%
CYP2D6 inhibition - 0.9017 90.17%
CYP1A2 inhibition - 0.7591 75.91%
CYP2C8 inhibition - 0.8940 89.40%
CYP inhibitory promiscuity - 0.7381 73.81%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6590 65.90%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.8905 89.05%
Skin irritation - 0.5895 58.95%
Skin corrosion - 0.9656 96.56%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4229 42.29%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.7002 70.02%
skin sensitisation - 0.6642 66.42%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6789 67.89%
Acute Oral Toxicity (c) III 0.8271 82.71%
Estrogen receptor binding - 0.5603 56.03%
Androgen receptor binding + 0.6234 62.34%
Thyroid receptor binding - 0.5862 58.62%
Glucocorticoid receptor binding - 0.4772 47.72%
Aromatase binding - 0.7108 71.08%
PPAR gamma - 0.6579 65.79%
Honey bee toxicity - 0.8947 89.47%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7450 74.50%
Fish aquatic toxicity + 0.9926 99.26%

Targets

Top

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 97.79% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.01% 97.25%
CHEMBL2581 P07339 Cathepsin D 94.78% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.96% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.03% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.21% 96.77%
CHEMBL3437 Q16853 Amine oxidase, copper containing 87.73% 94.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.61% 94.80%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.45% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.30% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.24% 93.04%
CHEMBL1937 Q92769 Histone deacetylase 2 84.76% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.25% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.86% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.15% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.07% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.87% 89.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.83% 90.17%
CHEMBL340 P08684 Cytochrome P450 3A4 82.18% 91.19%
CHEMBL1871 P10275 Androgen Receptor 80.07% 96.43%

Plants that contains it

Top
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.
Plectranthus montanus

Cross-Links

Top
PubChem 85240512
LOTUS LTS0222789
wikiData Q105215926