Bombamalone A

Details

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Internal ID dc56d75a-145f-4971-9907-140875a45ae0
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 5,10-dihydroxy-11-methoxy-10-methyl-7-propan-2-yl-2-oxatricyclo[6.3.1.04,12]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione
SMILES (Canonical) CC(C)C1=CC(=C2C3=C1C(=O)C(C(=C3OC2=O)OC)(C)O)O
SMILES (Isomeric) CC(C)C1=CC(=C2C3=C1C(=O)C(C(=C3OC2=O)OC)(C)O)O
InChI InChI=1S/C16H16O6/c1-6(2)7-5-8(17)10-11-9(7)13(18)16(3,20)14(21-4)12(11)22-15(10)19/h5-6,17,20H,1-4H3
InChI Key JYUFSZQBCUGFJN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O6
Molecular Weight 304.29 g/mol
Exact Mass 304.09468823 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.95
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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CHEMBL250449

2D Structure

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2D Structure of Bombamalone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 - 0.5140 51.40%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7979 79.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8709 87.09%
OATP1B3 inhibitior + 0.8851 88.51%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9151 91.51%
P-glycoprotein inhibitior - 0.8470 84.70%
P-glycoprotein substrate - 0.9139 91.39%
CYP3A4 substrate + 0.5481 54.81%
CYP2C9 substrate + 0.6223 62.23%
CYP2D6 substrate - 0.8692 86.92%
CYP3A4 inhibition - 0.6795 67.95%
CYP2C9 inhibition + 0.5874 58.74%
CYP2C19 inhibition - 0.6880 68.80%
CYP2D6 inhibition - 0.8505 85.05%
CYP1A2 inhibition - 0.5181 51.81%
CYP2C8 inhibition - 0.7308 73.08%
CYP inhibitory promiscuity + 0.6862 68.62%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9743 97.43%
Carcinogenicity (trinary) Danger 0.6019 60.19%
Eye corrosion - 0.9838 98.38%
Eye irritation + 0.7902 79.02%
Skin irritation - 0.7212 72.12%
Skin corrosion - 0.9412 94.12%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8347 83.47%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.5033 50.33%
skin sensitisation - 0.7705 77.05%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.6107 61.07%
Acute Oral Toxicity (c) III 0.4687 46.87%
Estrogen receptor binding + 0.6908 69.08%
Androgen receptor binding + 0.5886 58.86%
Thyroid receptor binding + 0.6077 60.77%
Glucocorticoid receptor binding + 0.6303 63.03%
Aromatase binding - 0.6156 61.56%
PPAR gamma + 0.6449 64.49%
Honey bee toxicity - 0.9084 90.84%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9920 99.20%

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 99.05% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.70% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 92.94% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.42% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.02% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.69% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 91.18% 94.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.12% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.81% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.24% 99.23%
CHEMBL4208 P20618 Proteasome component C5 86.66% 90.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.63% 91.07%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.60% 93.99%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.12% 97.21%
CHEMBL2535 P11166 Glucose transporter 83.18% 98.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.38% 96.21%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.47% 93.03%

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.
Bombax ceiba

Cross-Links

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PubChem 23642715
LOTUS LTS0242334
wikiData Q105137216