13-nor-Eudesm-5-en-11-one

Details

Top
Internal ID c3fea9b0-229b-43df-aa50-773df21f969d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name 1-[(4aS,8R)-4a,8-dimethyl-3,4,5,6,7,8-hexahydro-2H-naphthalen-2-yl]ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H22O/c1-10-5-4-7-14(3)8-6-12(11(2)15)9-13(10)14/h9-10,12H,4-8H2,1-3H3/t10-,12?,14+/m1/s1
InChI Key SEPLFXIHUVTSIX-HDDSUISISA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H22O
Molecular Weight 206.32 g/mol
Exact Mass 206.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.74
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
SEPLFXIHUVTSIX-HDDSUISISA-N

2D Structure

Top
2D Structure of 13-nor-Eudesm-5-en-11-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.9168 91.68%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.3989 39.89%
OATP2B1 inhibitior - 0.8442 84.42%
OATP1B1 inhibitior + 0.9107 91.07%
OATP1B3 inhibitior + 0.9570 95.70%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.6765 67.65%
P-glycoprotein inhibitior - 0.9320 93.20%
P-glycoprotein substrate - 0.9051 90.51%
CYP3A4 substrate + 0.5613 56.13%
CYP2C9 substrate - 0.8039 80.39%
CYP2D6 substrate - 0.7758 77.58%
CYP3A4 inhibition - 0.8768 87.68%
CYP2C9 inhibition - 0.6176 61.76%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.9338 93.38%
CYP1A2 inhibition - 0.7445 74.45%
CYP2C8 inhibition - 0.8951 89.51%
CYP inhibitory promiscuity - 0.6099 60.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.4935 49.35%
Eye corrosion - 0.9606 96.06%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.5700 57.00%
Skin corrosion - 0.9803 98.03%
Ames mutagenesis - 0.6723 67.23%
Human Ether-a-go-go-Related Gene inhibition - 0.6567 65.67%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.8023 80.23%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.7361 73.61%
Acute Oral Toxicity (c) III 0.7358 73.58%
Estrogen receptor binding - 0.8029 80.29%
Androgen receptor binding - 0.6781 67.81%
Thyroid receptor binding - 0.6662 66.62%
Glucocorticoid receptor binding - 0.7040 70.40%
Aromatase binding - 0.7579 75.79%
PPAR gamma - 0.9029 90.29%
Honey bee toxicity - 0.9505 95.05%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9921 99.21%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.70% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.95% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.77% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.24% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.81% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.38% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.31% 94.45%
CHEMBL2581 P07339 Cathepsin D 80.96% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.78% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.15% 100.00%

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.
Chrysopogon zizanioides

Cross-Links

Top
PubChem 6428322
LOTUS LTS0101083
wikiData Q104667186