Phomalairdenol D

Details

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Internal ID bb5bb8c6-60d1-4c6f-b63a-74958cd2443c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Triquinane sesquiterpenoids > Angular triquinanes
IUPAC Name (1R,4S,5S,8S,11R)-5,7,7,11-tetramethyltricyclo[6.3.0.01,5]undec-2-en-4-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10-5-6-11-13(2,3)9-14(4)12(16)7-8-15(10,11)14/h7-8,10-12,16H,5-6,9H2,1-4H3/t10-,11+,12+,14-,15+/m1/s1
InChI Key ZYETUZMHJIJQQT-NUNXZZDCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.39
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Phomalairdenol D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.6721 67.21%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.5059 50.59%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9330 93.30%
OATP1B3 inhibitior + 0.9072 90.72%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9599 95.99%
P-glycoprotein inhibitior - 0.9423 94.23%
P-glycoprotein substrate - 0.8626 86.26%
CYP3A4 substrate + 0.5074 50.74%
CYP2C9 substrate - 0.8008 80.08%
CYP2D6 substrate - 0.7219 72.19%
CYP3A4 inhibition - 0.8935 89.35%
CYP2C9 inhibition - 0.8576 85.76%
CYP2C19 inhibition - 0.8822 88.22%
CYP2D6 inhibition - 0.9591 95.91%
CYP1A2 inhibition - 0.6350 63.50%
CYP2C8 inhibition - 0.8731 87.31%
CYP inhibitory promiscuity - 0.9094 90.94%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6163 61.63%
Eye corrosion - 0.8814 88.14%
Eye irritation - 0.5919 59.19%
Skin irritation + 0.6786 67.86%
Skin corrosion - 0.9358 93.58%
Ames mutagenesis - 0.7015 70.15%
Human Ether-a-go-go-Related Gene inhibition - 0.6185 61.85%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation + 0.7851 78.51%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.5923 59.23%
Acute Oral Toxicity (c) III 0.7159 71.59%
Estrogen receptor binding - 0.5419 54.19%
Androgen receptor binding + 0.5322 53.22%
Thyroid receptor binding - 0.6539 65.39%
Glucocorticoid receptor binding - 0.8100 81.00%
Aromatase binding - 0.7856 78.56%
PPAR gamma - 0.7453 74.53%
Honey bee toxicity - 0.8877 88.77%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9771 97.71%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.10% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.13% 97.09%
CHEMBL2581 P07339 Cathepsin D 87.08% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.56% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.50% 95.89%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.20% 91.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.05% 97.25%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.69% 92.94%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139585683
LOTUS LTS0025303
wikiData Q77489316