Bonnadiene

Details

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Internal ID f88023ff-1e4a-4164-ab67-ea682362e997
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,9R,10R)-2,2,6,12-tetramethyl-9-propan-2-yltricyclo[8.4.0.01,5]tetradeca-5,11-diene
SMILES (Canonical) CC1=CC2C(CCC(=C3C2(CC1)C(CC3)(C)C)C)C(C)C
SMILES (Isomeric) CC1=C[C@H]2[C@H](CCC(=C3[C@]2(CC1)C(CC3)(C)C)C)C(C)C
InChI InChI=1S/C21H34/c1-14(2)17-8-7-16(4)18-10-11-20(5,6)21(18)12-9-15(3)13-19(17)21/h13-14,17,19H,7-12H2,1-6H3/t17-,19+,21+/m1/s1
InChI Key ODFAUAJALPIDBF-LMNJBCLMSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H34
Molecular Weight 286.50 g/mol
Exact Mass 286.266051085 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 6.53
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Bonnadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.9365 93.65%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.7289 72.89%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.8811 88.11%
OATP1B3 inhibitior + 0.9537 95.37%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6020 60.20%
P-glycoprotein inhibitior - 0.7859 78.59%
P-glycoprotein substrate - 0.8620 86.20%
CYP3A4 substrate + 0.5785 57.85%
CYP2C9 substrate - 0.6016 60.16%
CYP2D6 substrate - 0.7254 72.54%
CYP3A4 inhibition - 0.9170 91.70%
CYP2C9 inhibition - 0.7249 72.49%
CYP2C19 inhibition - 0.7247 72.47%
CYP2D6 inhibition - 0.9259 92.59%
CYP1A2 inhibition - 0.7863 78.63%
CYP2C8 inhibition - 0.8983 89.83%
CYP inhibitory promiscuity - 0.7182 71.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4675 46.75%
Eye corrosion - 0.9351 93.51%
Eye irritation - 0.5258 52.58%
Skin irritation + 0.5515 55.15%
Skin corrosion - 0.9710 97.10%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8368 83.68%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5728 57.28%
skin sensitisation + 0.8223 82.23%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6560 65.60%
Acute Oral Toxicity (c) III 0.7748 77.48%
Estrogen receptor binding - 0.6957 69.57%
Androgen receptor binding + 0.6872 68.72%
Thyroid receptor binding + 0.6476 64.76%
Glucocorticoid receptor binding - 0.5902 59.02%
Aromatase binding - 0.6059 60.59%
PPAR gamma - 0.6918 69.18%
Honey bee toxicity - 0.8076 80.76%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6300 63.00%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.97% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.73% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 90.46% 94.75%
CHEMBL1871 P10275 Androgen Receptor 89.69% 96.43%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.70% 91.11%
CHEMBL2581 P07339 Cathepsin D 86.62% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.29% 95.89%
CHEMBL259 P32245 Melanocortin receptor 4 85.44% 95.38%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.30% 100.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.81% 86.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.18% 95.56%
CHEMBL4444 P04070 Vitamin K-dependent protein C 80.34% 93.89%

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 139591546
LOTUS LTS0189496
wikiData Q105189792