Irisone B

Details

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Internal ID 27ae6d20-7c38-4af2-adbc-52d2d37dfdd8
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 9-hydroxy-7-(2-hydroxyphenyl)-[1,3]dioxolo[4,5-g]chromen-8-one
SMILES (Canonical) C1OC2=C(O1)C(=C3C(=C2)OC=C(C3=O)C4=CC=CC=C4O)O
SMILES (Isomeric) C1OC2=C(O1)C(=C3C(=C2)OC=C(C3=O)C4=CC=CC=C4O)O
InChI InChI=1S/C16H10O6/c17-10-4-2-1-3-8(10)9-6-20-11-5-12-16(22-7-21-12)15(19)13(11)14(9)18/h1-6,17,19H,7H2
InChI Key ITRQVDOUFMSYII-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C16H10O6
Molecular Weight 298.25 g/mol
Exact Mass 298.04773803 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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5,2'-Dihydroxy-6,7-methylenedioxyisoflavone
97359-75-6
2',5-Dihydroxy-6,7-methylenedioxyisoflavone
CHEMBL443974
DTXSID30242895
LMPK12050366
NSC621635
AKOS032961815
NSC-621635
8H-1,3-Dioxolo(4,5-g)(1)benzopyran-8-one, 9-hydroxy-7-(2-hydroxyphenyl)-

2D Structure

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2D Structure of Irisone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9455 94.55%
Caco-2 - 0.6603 66.03%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8322 83.22%
OATP2B1 inhibitior - 0.5730 57.30%
OATP1B1 inhibitior + 0.9528 95.28%
OATP1B3 inhibitior + 0.8872 88.72%
MATE1 inhibitior + 0.6200 62.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7568 75.68%
P-glycoprotein inhibitior - 0.4753 47.53%
P-glycoprotein substrate - 0.9205 92.05%
CYP3A4 substrate - 0.5129 51.29%
CYP2C9 substrate - 0.6133 61.33%
CYP2D6 substrate - 0.8612 86.12%
CYP3A4 inhibition + 0.5998 59.98%
CYP2C9 inhibition + 0.8211 82.11%
CYP2C19 inhibition + 0.5194 51.94%
CYP2D6 inhibition - 0.6831 68.31%
CYP1A2 inhibition - 0.5351 53.51%
CYP2C8 inhibition - 0.6544 65.44%
CYP inhibitory promiscuity + 0.6864 68.64%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5447 54.47%
Eye corrosion - 0.9912 99.12%
Eye irritation + 0.9302 93.02%
Skin irritation - 0.6180 61.80%
Skin corrosion - 0.9546 95.46%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8491 84.91%
Micronuclear + 0.8774 87.74%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8524 85.24%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.4643 46.43%
Acute Oral Toxicity (c) III 0.3669 36.69%
Estrogen receptor binding + 0.8298 82.98%
Androgen receptor binding + 0.8181 81.81%
Thyroid receptor binding + 0.6525 65.25%
Glucocorticoid receptor binding + 0.8320 83.20%
Aromatase binding + 0.8642 86.42%
PPAR gamma + 0.9194 91.94%
Honey bee toxicity - 0.8511 85.11%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9479 94.79%

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 99.44% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.27% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.20% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.69% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.36% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.78% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.53% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.39% 94.00%
CHEMBL4208 P20618 Proteasome component C5 84.40% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.37% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 80.86% 94.73%
CHEMBL2535 P11166 Glucose transporter 80.51% 98.75%

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.
Bassia scoparia
Blutaparon portulacoides
Iris missouriensis
Iris songarica
Iris tenuifolia
Salsola collina

Cross-Links

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PubChem 5387194
NPASS NPC225624
LOTUS LTS0107846
wikiData Q83126774