Abyssinone III

Details

Top
Internal ID 7a462dca-32af-49ab-9fd7-3cc5942a8f14
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 3-prenylated flavans > 3-prenylated flavanones
IUPAC Name 2-[2,2-dimethyl-8-(3-methylbut-2-enyl)chromen-6-yl]-7-hydroxy-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H26O4/c1-15(2)5-6-16-11-18(12-17-9-10-25(3,4)29-24(16)17)22-14-21(27)20-8-7-19(26)13-23(20)28-22/h5,7-13,22,26H,6,14H2,1-4H3
InChI Key BWSXMPVDLMJKKY-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C25H26O4
Molecular Weight 390.50 g/mol
Exact Mass 390.18310931 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.79
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
CHEMBL1688179
LMPK12140051

2D Structure

Top
2D Structure of Abyssinone III

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.5266 52.66%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8197 81.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8174 81.74%
OATP1B3 inhibitior + 0.9527 95.27%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9505 95.05%
P-glycoprotein inhibitior + 0.8222 82.22%
P-glycoprotein substrate + 0.6316 63.16%
CYP3A4 substrate + 0.6580 65.80%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.7542 75.42%
CYP3A4 inhibition - 0.6735 67.35%
CYP2C9 inhibition + 0.6989 69.89%
CYP2C19 inhibition + 0.8039 80.39%
CYP2D6 inhibition - 0.8751 87.51%
CYP1A2 inhibition - 0.7447 74.47%
CYP2C8 inhibition + 0.5805 58.05%
CYP inhibitory promiscuity + 0.7179 71.79%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9513 95.13%
Carcinogenicity (trinary) Non-required 0.6275 62.75%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.7739 77.39%
Skin irritation - 0.7297 72.97%
Skin corrosion - 0.9506 95.06%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7880 78.80%
Micronuclear - 0.6041 60.41%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.6867 68.67%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5637 56.37%
Acute Oral Toxicity (c) III 0.6830 68.30%
Estrogen receptor binding + 0.9441 94.41%
Androgen receptor binding + 0.6797 67.97%
Thyroid receptor binding + 0.6273 62.73%
Glucocorticoid receptor binding + 0.8441 84.41%
Aromatase binding + 0.5999 59.99%
PPAR gamma + 0.8463 84.63%
Honey bee toxicity - 0.7345 73.45%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9775 97.75%

Targets

Top

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 99.60% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.67% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.13% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.79% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.59% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.69% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.62% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.55% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 89.33% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.30% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.04% 95.56%
CHEMBL4208 P20618 Proteasome component C5 85.42% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.25% 95.89%
CHEMBL236 P41143 Delta opioid receptor 84.56% 99.35%
CHEMBL1951 P21397 Monoamine oxidase A 84.12% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 83.65% 94.73%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.95% 97.28%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.31% 90.71%

Plants that contains it

Top
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.
Erythrina abyssinica
Erythrina mildbraedii

Cross-Links

Top
PubChem 42607817
LOTUS LTS0216445
wikiData Q104249735