(+)-Eudesma-5,7(11)-diene

Details

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Internal ID 37d75b2f-372a-4146-8b1f-cd0bcc50f1e7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,4a-dimethyl-7-propan-2-ylidene-1,2,3,4,5,6-hexahydronaphthalene
SMILES (Canonical) CC1CCCC2(C1=CC(=C(C)C)CC2)C
SMILES (Isomeric) CC1CCCC2(C1=CC(=C(C)C)CC2)C
InChI InChI=1S/C15H24/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h10,12H,5-9H2,1-4H3
InChI Key ZQODGIAJYWHYRF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.87
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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ZQODGIAJYWHYRF-UHFFFAOYSA-N

2D Structure

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2D Structure of (+)-Eudesma-5,7(11)-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.9277 92.77%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.6409 64.09%
OATP2B1 inhibitior - 0.8452 84.52%
OATP1B1 inhibitior + 0.9240 92.40%
OATP1B3 inhibitior + 0.9233 92.33%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7249 72.49%
P-glycoprotein inhibitior - 0.9384 93.84%
P-glycoprotein substrate - 0.8702 87.02%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8001 80.01%
CYP2D6 substrate - 0.7763 77.63%
CYP3A4 inhibition - 0.8836 88.36%
CYP2C9 inhibition - 0.6480 64.80%
CYP2C19 inhibition - 0.5487 54.87%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.8497 84.97%
CYP2C8 inhibition - 0.8233 82.33%
CYP inhibitory promiscuity - 0.6076 60.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.4643 46.43%
Eye corrosion - 0.9401 94.01%
Eye irritation + 0.6644 66.44%
Skin irritation - 0.6654 66.54%
Skin corrosion - 0.9532 95.32%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4204 42.04%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5642 56.42%
skin sensitisation + 0.8350 83.50%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.8608 86.08%
Acute Oral Toxicity (c) III 0.7287 72.87%
Estrogen receptor binding - 0.8496 84.96%
Androgen receptor binding + 0.6076 60.76%
Thyroid receptor binding - 0.6353 63.53%
Glucocorticoid receptor binding - 0.7620 76.20%
Aromatase binding - 0.7481 74.81%
PPAR gamma - 0.8266 82.66%
Honey bee toxicity - 0.9370 93.70%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.13% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.79% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.55% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 92.62% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.91% 100.00%
CHEMBL2581 P07339 Cathepsin D 83.75% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.72% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.49% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.31% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.14% 95.89%

Cross-Links

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PubChem 6428860
NPASS NPC78207
LOTUS LTS0133038
wikiData Q104667263