(5beta,6alpha)-6,11-Dihydroxyeudesmane

Details

Top
Internal ID f5901be9-39d0-4392-afbc-c78657ea717c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (1R,2R,4aR,8R,8aR)-2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H28O2/c1-10-6-5-8-15(4)9-7-11(14(2,3)17)13(16)12(10)15/h10-13,16-17H,5-9H2,1-4H3/t10-,11-,12+,13+,15-/m1/s1
InChI Key HGRCRWYTMFSGFV-DGMCESFYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H28O2
Molecular Weight 240.38 g/mol
Exact Mass 240.208930132 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 4.10
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (5beta,6alpha)-6,11-Dihydroxyeudesmane

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 + 0.6899 68.99%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5125 51.25%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9393 93.93%
OATP1B3 inhibitior + 0.9307 93.07%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8326 83.26%
P-glycoprotein inhibitior - 0.9185 91.85%
P-glycoprotein substrate - 0.9015 90.15%
CYP3A4 substrate + 0.5462 54.62%
CYP2C9 substrate + 0.5942 59.42%
CYP2D6 substrate - 0.7034 70.34%
CYP3A4 inhibition - 0.8850 88.50%
CYP2C9 inhibition - 0.6743 67.43%
CYP2C19 inhibition - 0.7519 75.19%
CYP2D6 inhibition - 0.9472 94.72%
CYP1A2 inhibition + 0.5522 55.22%
CYP2C8 inhibition - 0.8298 82.98%
CYP inhibitory promiscuity - 0.8152 81.52%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6570 65.70%
Eye corrosion - 0.9583 95.83%
Eye irritation - 0.6021 60.21%
Skin irritation - 0.5658 56.58%
Skin corrosion - 0.9112 91.12%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7584 75.84%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation - 0.5312 53.12%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7963 79.63%
Acute Oral Toxicity (c) III 0.7770 77.70%
Estrogen receptor binding - 0.5646 56.46%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.6206 62.06%
Glucocorticoid receptor binding - 0.5122 51.22%
Aromatase binding - 0.7254 72.54%
PPAR gamma - 0.7641 76.41%
Honey bee toxicity - 0.8561 85.61%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9756 97.56%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.80% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.83% 92.94%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.37% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.12% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.99% 97.09%
CHEMBL2581 P07339 Cathepsin D 85.41% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.10% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.42% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.26% 95.89%
CHEMBL5600 P27448 Serine/threonine-protein kinase c-TAK1 81.20% 88.81%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.21% 82.69%
CHEMBL2996 Q05655 Protein kinase C delta 80.08% 97.79%

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.
There are no matching plants.

Cross-Links

Top
PubChem 102033116
LOTUS LTS0225249
wikiData Q77491353