10-epi-Eudesmol

Details

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Internal ID 2809b6c8-4027-497e-9ed5-944cfe4890d1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name 2-[(2R,4aS)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol
SMILES (Canonical) CC1=CCCC2(C1CC(CC2)C(C)(C)O)C
SMILES (Isomeric) CC1=CCC[C@@]2(C1C[C@@H](CC2)C(C)(C)O)C
InChI InChI=1S/C15H26O/c1-11-6-5-8-15(4)9-7-12(10-13(11)15)14(2,3)16/h6,12-13,16H,5,7-10H2,1-4H3/t12-,13?,15+/m1/s1
InChI Key FCSRUSQUAVXUKK-JHIQODARSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.92
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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FCSRUSQUAVXUKK-JHIQODARSA-N

2D Structure

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2D Structure of 10-epi-Eudesmol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8084 80.84%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4513 45.13%
OATP2B1 inhibitior - 0.8457 84.57%
OATP1B1 inhibitior + 0.9391 93.91%
OATP1B3 inhibitior + 0.8318 83.18%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7030 70.30%
P-glycoprotein inhibitior - 0.9474 94.74%
P-glycoprotein substrate - 0.8773 87.73%
CYP3A4 substrate + 0.5334 53.34%
CYP2C9 substrate + 0.5024 50.24%
CYP2D6 substrate - 0.7533 75.33%
CYP3A4 inhibition - 0.8252 82.52%
CYP2C9 inhibition + 0.5834 58.34%
CYP2C19 inhibition + 0.6144 61.44%
CYP2D6 inhibition - 0.9183 91.83%
CYP1A2 inhibition - 0.7987 79.87%
CYP2C8 inhibition - 0.5715 57.15%
CYP inhibitory promiscuity - 0.6206 62.06%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.5965 59.65%
Eye corrosion - 0.9692 96.92%
Eye irritation - 0.7208 72.08%
Skin irritation + 0.5138 51.38%
Skin corrosion - 0.9641 96.41%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5738 57.38%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5588 55.88%
skin sensitisation + 0.8232 82.32%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6133 61.33%
Acute Oral Toxicity (c) III 0.5137 51.37%
Estrogen receptor binding - 0.8369 83.69%
Androgen receptor binding - 0.7890 78.90%
Thyroid receptor binding - 0.6649 66.49%
Glucocorticoid receptor binding - 0.5808 58.08%
Aromatase binding - 0.8704 87.04%
PPAR gamma - 0.7725 77.25%
Honey bee toxicity - 0.8856 88.56%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.9936 99.36%

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 99.08% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.00% 97.09%
CHEMBL1871 P10275 Androgen Receptor 90.14% 96.43%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.71% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.67% 96.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 88.14% 93.04%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.99% 92.94%
CHEMBL2996 Q05655 Protein kinase C delta 84.11% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.10% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.59% 95.89%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 80.52% 90.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.16% 95.56%

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.
Magnolia biondii

Cross-Links

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PubChem 6428994
NPASS NPC253528