Isoamoritin

Details

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Internal ID 849887c8-2dd3-4158-a134-ee4299080c40
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > 8-prenylated flavans > 8-prenylated flavanones
IUPAC Name (2S)-5,7-dihydroxy-2-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one
SMILES (Canonical) CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C(=C(C(=C3O2)CC=C(C)C)O)CC=C(C)C)O)O)OC)C
SMILES (Isomeric) CC(=CCC1=C(C(=CC(=C1)[C@@H]2CC(=O)C3=C(C(=C(C(=C3O2)CC=C(C)C)O)CC=C(C)C)O)O)OC)C
InChI InChI=1S/C31H38O6/c1-17(2)8-11-20-14-21(15-25(33)30(20)36-7)26-16-24(32)27-29(35)22(12-9-18(3)4)28(34)23(31(27)37-26)13-10-19(5)6/h8-10,14-15,26,33-35H,11-13,16H2,1-7H3/t26-/m0/s1
InChI Key YSSBXXIEFDCVDX-SANMLTNESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C31H38O6
Molecular Weight 506.60 g/mol
Exact Mass 506.26683893 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 8.10
Atomic LogP (AlogP) 7.04
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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5,7,3'-Trihydroxy-4'-methoxy-6,8,5'-triprenylflavanone
CHEBI:184709
LMPK12140384
(2S)-5,7-dihydroxy-2-[3-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

2D Structure

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2D Structure of Isoamoritin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9727 97.27%
Caco-2 - 0.6208 62.08%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6168 61.68%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.8642 86.42%
OATP1B3 inhibitior + 0.9112 91.12%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9231 92.31%
P-glycoprotein inhibitior + 0.7964 79.64%
P-glycoprotein substrate - 0.7973 79.73%
CYP3A4 substrate + 0.5977 59.77%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.7912 79.12%
CYP3A4 inhibition - 0.7416 74.16%
CYP2C9 inhibition + 0.7992 79.92%
CYP2C19 inhibition + 0.8459 84.59%
CYP2D6 inhibition + 0.6194 61.94%
CYP1A2 inhibition + 0.7633 76.33%
CYP2C8 inhibition - 0.6103 61.03%
CYP inhibitory promiscuity + 0.8463 84.63%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7303 73.03%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.8764 87.64%
Skin irritation - 0.7796 77.96%
Skin corrosion - 0.9467 94.67%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8476 84.76%
Micronuclear - 0.5400 54.00%
Hepatotoxicity - 0.5072 50.72%
skin sensitisation - 0.8301 83.01%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.8011 80.11%
Acute Oral Toxicity (c) III 0.4382 43.82%
Estrogen receptor binding + 0.8947 89.47%
Androgen receptor binding + 0.6123 61.23%
Thyroid receptor binding + 0.6508 65.08%
Glucocorticoid receptor binding + 0.8684 86.84%
Aromatase binding + 0.6697 66.97%
PPAR gamma + 0.6994 69.94%
Honey bee toxicity - 0.7432 74.32%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9866 98.66%

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 99.80% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.82% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.99% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.12% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.61% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.26% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.88% 86.33%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 86.24% 92.68%
CHEMBL3401 O75469 Pregnane X receptor 86.13% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.41% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.00% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.80% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.62% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.83% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.42% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.55% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.77% 99.23%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.57% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.41% 96.95%

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.
Amorpha fruticosa

Cross-Links

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PubChem 42607986
LOTUS LTS0209730
wikiData Q105360617