Azadiradione,2B-diepoxy-

Details

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Internal ID b9c34794-83ca-492b-b104-671f1bb9b8ee
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name [16-(furan-3-yl)-2,7,7,11,17-pentamethyl-6,15-dioxo-4,13-dioxahexacyclo[9.8.0.02,8.03,5.012,14.012,17]nonadecan-10-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H34O7/c1-13(29)33-17-11-16-24(2,3)21(31)20-23(34-20)26(16,5)15-7-9-25(4)18(14-8-10-32-12-14)19(30)22-28(25,35-22)27(15,17)6/h8,10,12,15-18,20,22-23H,7,9,11H2,1-6H3
InChI Key IRLGUCNVQLHFII-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H34O7
Molecular Weight 482.60 g/mol
Exact Mass 482.23045342 g/mol
Topological Polar Surface Area (TPSA) 98.60 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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AZADIRADIONE,2B-DIEPOXY-
NSC-349982

2D Structure

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2D Structure of Azadiradione,2B-diepoxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9767 97.67%
Caco-2 - 0.6158 61.58%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7333 73.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior - 0.5894 58.94%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6345 63.45%
P-glycoprotein inhibitior + 0.7208 72.08%
P-glycoprotein substrate - 0.6001 60.01%
CYP3A4 substrate + 0.7121 71.21%
CYP2C9 substrate + 0.5898 58.98%
CYP2D6 substrate - 0.8258 82.58%
CYP3A4 inhibition + 0.7625 76.25%
CYP2C9 inhibition - 0.8029 80.29%
CYP2C19 inhibition - 0.7428 74.28%
CYP2D6 inhibition - 0.9305 93.05%
CYP1A2 inhibition - 0.8124 81.24%
CYP2C8 inhibition + 0.7097 70.97%
CYP inhibitory promiscuity - 0.9043 90.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5627 56.27%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.8958 89.58%
Skin irritation - 0.7139 71.39%
Skin corrosion - 0.8375 83.75%
Ames mutagenesis - 0.6383 63.83%
Human Ether-a-go-go-Related Gene inhibition + 0.7726 77.26%
Micronuclear - 0.6500 65.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.8282 82.82%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.7642 76.42%
Acute Oral Toxicity (c) III 0.4174 41.74%
Estrogen receptor binding + 0.8860 88.60%
Androgen receptor binding + 0.7469 74.69%
Thyroid receptor binding + 0.7233 72.33%
Glucocorticoid receptor binding + 0.8448 84.48%
Aromatase binding + 0.7858 78.58%
PPAR gamma + 0.7766 77.66%
Honey bee toxicity - 0.7929 79.29%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9819 98.19%

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 98.53% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.22% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.12% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.68% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.11% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.96% 86.33%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.62% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.34% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 87.85% 93.04%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.57% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.43% 94.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 85.58% 97.28%
CHEMBL340 P08684 Cytochrome P450 3A4 85.12% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.87% 100.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.16% 97.14%
CHEMBL5028 O14672 ADAM10 83.80% 97.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.26% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.19% 95.89%

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.
Azadirachta indica

Cross-Links

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PubChem 336301
LOTUS LTS0035093
wikiData Q105118933