Isoanhydroicaritin

Details

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Internal ID 573f44da-2339-450b-8a4d-80a5428f636d
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 8-prenylated flavones
IUPAC Name 3,5-dihydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C
SMILES (Isomeric) CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C
InChI InChI=1S/C21H20O6/c1-11(2)4-9-14-16(26-3)10-15(23)17-18(24)19(25)20(27-21(14)17)12-5-7-13(22)8-6-12/h4-8,10,22-23,25H,9H2,1-3H3
InChI Key RJANATGWWPNKAL-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H20O6
Molecular Weight 368.40 g/mol
Exact Mass 368.12598835 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.09
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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28610-30-2
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)chromen-4-one
4',5-Dihydroxy-7-methoxy-8-prenylflavonol
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one
SCHEMBL563464
HY-N6044
LMPK12112587
AKOS037514698
CS-0032233
3,4',5-trihydroxy-7-methoxy-8-prenylflavone

2D Structure

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2D Structure of Isoanhydroicaritin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9894 98.94%
Caco-2 + 0.6538 65.38%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7007 70.07%
OATP2B1 inhibitior - 0.5615 56.15%
OATP1B1 inhibitior + 0.8742 87.42%
OATP1B3 inhibitior + 0.8634 86.34%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8502 85.02%
P-glycoprotein inhibitior + 0.7110 71.10%
P-glycoprotein substrate - 0.5863 58.63%
CYP3A4 substrate + 0.5867 58.67%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.8014 80.14%
CYP2C9 inhibition + 0.8898 88.98%
CYP2C19 inhibition + 0.9435 94.35%
CYP2D6 inhibition - 0.5726 57.26%
CYP1A2 inhibition + 0.7497 74.97%
CYP2C8 inhibition + 0.8147 81.47%
CYP inhibitory promiscuity + 0.9246 92.46%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6363 63.63%
Eye corrosion - 0.9895 98.95%
Eye irritation + 0.5739 57.39%
Skin irritation - 0.7699 76.99%
Skin corrosion - 0.9621 96.21%
Ames mutagenesis + 0.6163 61.63%
Human Ether-a-go-go-Related Gene inhibition - 0.5843 58.43%
Micronuclear + 0.5100 51.00%
Hepatotoxicity + 0.5552 55.52%
skin sensitisation - 0.8209 82.09%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6555 65.55%
Acute Oral Toxicity (c) III 0.7315 73.15%
Estrogen receptor binding + 0.8709 87.09%
Androgen receptor binding + 0.8089 80.89%
Thyroid receptor binding + 0.5902 59.02%
Glucocorticoid receptor binding + 0.8564 85.64%
Aromatase binding + 0.7276 72.76%
PPAR gamma + 0.9342 93.42%
Honey bee toxicity - 0.7606 76.06%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9888 98.88%

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 99.48% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.11% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.86% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.96% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.92% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.81% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 91.73% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.41% 99.17%
CHEMBL3194 P02766 Transthyretin 90.63% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.34% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.62% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.14% 99.15%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 83.74% 98.11%
CHEMBL1937 Q92769 Histone deacetylase 2 83.22% 94.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.02% 96.95%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 82.79% 95.64%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.78% 95.89%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.34% 91.71%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.13% 97.28%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.86% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.13% 95.50%

Cross-Links

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PubChem 5322079
NPASS NPC44745
LOTUS LTS0091991
wikiData Q105237329