1-(2,4a,8-Trihydroxy-1,2,6-trimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)-3-hydroxy-1-propanone

Details

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Internal ID 66148064-a312-44fe-87a2-596de458b670
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones > Beta-hydroxy ketones
IUPAC Name 1-(2,4a,8-trihydroxy-1,2,6-trimethyl-6,7,8,8a-tetrahydro-5H-naphthalen-1-yl)-3-hydroxypropan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H26O5/c1-10-8-11(18)13-15(3,12(19)4-7-17)14(2,20)5-6-16(13,21)9-10/h5-6,10-11,13,17-18,20-21H,4,7-9H2,1-3H3
InChI Key XLPZAZKGKJAESI-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H26O5
Molecular Weight 298.37 g/mol
Exact Mass 298.17802393 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.40
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(2,4a,8-Trihydroxy-1,2,6-trimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)-3-hydroxy-1-propanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9779 97.79%
Caco-2 + 0.6790 67.90%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.5671 56.71%
OATP2B1 inhibitior - 0.8587 85.87%
OATP1B1 inhibitior + 0.9063 90.63%
OATP1B3 inhibitior + 0.9112 91.12%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6473 64.73%
BSEP inhibitior - 0.6450 64.50%
P-glycoprotein inhibitior - 0.9541 95.41%
P-glycoprotein substrate - 0.6523 65.23%
CYP3A4 substrate + 0.5758 57.58%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8392 83.92%
CYP3A4 inhibition - 0.5812 58.12%
CYP2C9 inhibition - 0.8551 85.51%
CYP2C19 inhibition - 0.8963 89.63%
CYP2D6 inhibition - 0.9384 93.84%
CYP1A2 inhibition - 0.7149 71.49%
CYP2C8 inhibition - 0.8977 89.77%
CYP inhibitory promiscuity - 0.8715 87.15%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7200 72.00%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9659 96.59%
Skin irritation + 0.4903 49.03%
Skin corrosion - 0.9513 95.13%
Ames mutagenesis - 0.6654 66.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6845 68.45%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5535 55.35%
skin sensitisation - 0.8250 82.50%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6355 63.55%
Acute Oral Toxicity (c) III 0.7803 78.03%
Estrogen receptor binding - 0.5916 59.16%
Androgen receptor binding + 0.5365 53.65%
Thyroid receptor binding + 0.6253 62.53%
Glucocorticoid receptor binding - 0.5535 55.35%
Aromatase binding + 0.6521 65.21%
PPAR gamma - 0.7151 71.51%
Honey bee toxicity - 0.7551 75.51%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.8886 88.86%

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 98.46% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.19% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.50% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 89.50% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.27% 97.09%
CHEMBL299 P17252 Protein kinase C alpha 84.59% 98.03%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.94% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.75% 100.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 80.08% 91.24%

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 78099848
LOTUS LTS0162942
wikiData Q104201107