1-(2,4-Dihydroxy-4a,8,8-trimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl)ethanone

Details

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Internal ID ed3c2f17-039a-427a-b8a7-519e289cefd4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclic alcohols and derivatives
IUPAC Name 1-(2,4-dihydroxy-4a,8,8-trimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl)ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O3/c1-9(16)12-10(17)8-11(18)15(4)7-5-6-14(2,3)13(12)15/h10-13,17-18H,5-8H2,1-4H3
InChI Key FIPQUFXNPGNDFR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O3
Molecular Weight 254.36 g/mol
Exact Mass 254.18819469 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.15
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-(2,4-Dihydroxy-4a,8,8-trimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-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 + 0.9931 99.31%
Caco-2 + 0.5850 58.50%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7344 73.44%
OATP2B1 inhibitior - 0.8442 84.42%
OATP1B1 inhibitior + 0.8873 88.73%
OATP1B3 inhibitior + 0.9618 96.18%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9247 92.47%
P-glycoprotein inhibitior - 0.8596 85.96%
P-glycoprotein substrate - 0.8594 85.94%
CYP3A4 substrate + 0.5880 58.80%
CYP2C9 substrate - 0.8408 84.08%
CYP2D6 substrate - 0.7400 74.00%
CYP3A4 inhibition - 0.7935 79.35%
CYP2C9 inhibition - 0.6489 64.89%
CYP2C19 inhibition - 0.8745 87.45%
CYP2D6 inhibition - 0.9620 96.20%
CYP1A2 inhibition - 0.7395 73.95%
CYP2C8 inhibition - 0.9294 92.94%
CYP inhibitory promiscuity - 0.9477 94.77%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6406 64.06%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.5355 53.55%
Skin irritation + 0.5822 58.22%
Skin corrosion - 0.9239 92.39%
Ames mutagenesis - 0.7244 72.44%
Human Ether-a-go-go-Related Gene inhibition - 0.7123 71.23%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.6391 63.91%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6445 64.45%
Acute Oral Toxicity (c) III 0.5302 53.02%
Estrogen receptor binding + 0.5456 54.56%
Androgen receptor binding - 0.5161 51.61%
Thyroid receptor binding - 0.5153 51.53%
Glucocorticoid receptor binding - 0.5751 57.51%
Aromatase binding - 0.6426 64.26%
PPAR gamma - 0.7717 77.17%
Honey bee toxicity - 0.8306 83.06%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9611 96.11%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.97% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.86% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.86% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.04% 94.45%
CHEMBL340 P08684 Cytochrome P450 3A4 84.44% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.63% 100.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.08% 96.38%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.58% 93.04%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.52% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.41% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.71% 82.69%

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.
Illicium micranthum subsp. tsangii

Cross-Links

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PubChem 85272695
LOTUS LTS0031229
wikiData Q104995814