Isoiriskashmirianin

Details

Top
Internal ID c9588335-d6f9-4722-a19e-5d2c4806afc9
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 3-O-methylated isoflavonoids > 3-O-methylisoflavones
IUPAC Name 7-(3-hydroxy-5-methoxyphenyl)-9-methoxy-[1,3]dioxolo[4,5-g]chromen-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H14O7/c1-21-11-4-9(3-10(19)5-11)12-7-23-13-6-14-17(25-8-24-14)18(22-2)15(13)16(12)20/h3-7,19H,8H2,1-2H3
InChI Key DLVQIIYSDXYGEG-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C18H14O7
Molecular Weight 342.30 g/mol
Exact Mass 342.07395278 g/mol
Topological Polar Surface Area (TPSA) 83.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.91
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
3'-Hydroxy-5,5'-dimethoxy-6,7-methylenedioxyisoflavone
LMPK12050370

2D Structure

Top
2D Structure of Isoiriskashmirianin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9794 97.94%
Caco-2 + 0.7792 77.92%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8101 81.01%
OATP2B1 inhibitior - 0.8632 86.32%
OATP1B1 inhibitior + 0.9515 95.15%
OATP1B3 inhibitior + 0.9172 91.72%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4729 47.29%
P-glycoprotein inhibitior + 0.7842 78.42%
P-glycoprotein substrate - 0.8732 87.32%
CYP3A4 substrate + 0.5678 56.78%
CYP2C9 substrate - 0.8253 82.53%
CYP2D6 substrate - 0.8058 80.58%
CYP3A4 inhibition + 0.8906 89.06%
CYP2C9 inhibition + 0.8811 88.11%
CYP2C19 inhibition + 0.8944 89.44%
CYP2D6 inhibition + 0.6487 64.87%
CYP1A2 inhibition - 0.7054 70.54%
CYP2C8 inhibition - 0.5642 56.42%
CYP inhibitory promiscuity + 0.8415 84.15%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4819 48.19%
Eye corrosion - 0.9842 98.42%
Eye irritation - 0.5787 57.87%
Skin irritation - 0.7505 75.05%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis - 0.5454 54.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7140 71.40%
Micronuclear + 0.8674 86.74%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8088 80.88%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.5277 52.77%
Acute Oral Toxicity (c) III 0.5795 57.95%
Estrogen receptor binding + 0.8604 86.04%
Androgen receptor binding + 0.7220 72.20%
Thyroid receptor binding + 0.6362 63.62%
Glucocorticoid receptor binding + 0.8329 83.29%
Aromatase binding + 0.7792 77.92%
PPAR gamma + 0.8435 84.35%
Honey bee toxicity - 0.7985 79.85%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9243 92.43%

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 99.05% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.42% 96.77%
CHEMBL2581 P07339 Cathepsin D 94.80% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.75% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.76% 94.00%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 91.53% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.90% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.20% 94.45%
CHEMBL4208 P20618 Proteasome component C5 89.57% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.03% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.84% 86.33%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.32% 94.42%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.72% 85.14%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 85.63% 82.67%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.57% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.42% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.74% 96.09%
CHEMBL2535 P11166 Glucose transporter 81.07% 98.75%
CHEMBL1929 P47989 Xanthine dehydrogenase 80.96% 96.12%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.74% 99.17%

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.
Iris kashmiriana

Cross-Links

Top
PubChem 14539328
LOTUS LTS0048505
wikiData Q104984741