(4aR,5S,8S,8aR)-4a,5-dihydroxy-3,8-dimethyl-5-propan-2-yl-1,7,8,8a-tetrahydronaphthalene-2,6-dione

Details

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Internal ID b0196dc3-cab9-4b33-830d-c10ac85ed123
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4aR,5S,8S,8aR)-4a,5-dihydroxy-3,8-dimethyl-5-propan-2-yl-1,7,8,8a-tetrahydronaphthalene-2,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O4/c1-8(2)15(19)13(17)5-9(3)11-6-12(16)10(4)7-14(11,15)18/h7-9,11,18-19H,5-6H2,1-4H3/t9-,11+,14-,15+/m0/s1
InChI Key UBJXFLRRWCBXGH-OCVOHJKQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O4
Molecular Weight 266.33 g/mol
Exact Mass 266.15180918 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.25
H-Bond Acceptor 4
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 (4aR,5S,8S,8aR)-4a,5-dihydroxy-3,8-dimethyl-5-propan-2-yl-1,7,8,8a-tetrahydronaphthalene-2,6-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.6988 69.88%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7986 79.86%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9329 93.29%
OATP1B3 inhibitior + 0.8883 88.83%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9223 92.23%
P-glycoprotein inhibitior - 0.9406 94.06%
P-glycoprotein substrate - 0.8287 82.87%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8619 86.19%
CYP3A4 inhibition - 0.6096 60.96%
CYP2C9 inhibition - 0.8654 86.54%
CYP2C19 inhibition - 0.8433 84.33%
CYP2D6 inhibition - 0.9267 92.67%
CYP1A2 inhibition - 0.8091 80.91%
CYP2C8 inhibition - 0.9727 97.27%
CYP inhibitory promiscuity - 0.9051 90.51%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5573 55.73%
Eye corrosion - 0.9913 99.13%
Eye irritation - 0.8049 80.49%
Skin irritation - 0.5553 55.53%
Skin corrosion - 0.9338 93.38%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.5880 58.80%
skin sensitisation - 0.5659 56.59%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6625 66.25%
Acute Oral Toxicity (c) III 0.4688 46.88%
Estrogen receptor binding + 0.5293 52.93%
Androgen receptor binding + 0.5291 52.91%
Thyroid receptor binding - 0.5107 51.07%
Glucocorticoid receptor binding - 0.6499 64.99%
Aromatase binding - 0.6301 63.01%
PPAR gamma - 0.8335 83.35%
Honey bee toxicity - 0.8989 89.89%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9948 99.48%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.87% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.63% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.92% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 90.79% 94.75%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 90.46% 93.04%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.40% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.53% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.59% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.08% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.75% 82.69%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.66% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.37% 93.56%

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.
Ageratina adenophora
Croton tiglium

Cross-Links

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PubChem 102039327
NPASS NPC63141
LOTUS LTS0099709
wikiData Q105269395