Iristectorigenin A

Details

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Internal ID 825eefbc-fc4f-4e73-8187-0c32042af09e
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 3-O-methylated isoflavonoids > 3-O-methylisoflavones
IUPAC Name 5,7-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-6-methoxychromen-4-one
SMILES (Canonical) COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)OC)O)O
InChI InChI=1S/C17H14O7/c1-22-12-5-8(3-4-10(12)18)9-7-24-13-6-11(19)17(23-2)16(21)14(13)15(9)20/h3-7,18-19,21H,1-2H3
InChI Key CCRPIWFQMLICCY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H14O7
Molecular Weight 330.29 g/mol
Exact Mass 330.07395278 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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39012-01-6
5,7-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-6-methoxychromen-4-one
5,7,4'-Trihydroxy-6,3'-dimethoxyisoflavone
4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-6-methoxy-
5,7-Dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-6-methoxy-4H-1-benzopyran-4-one
5,7-Dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-6-methoxy-4H-chromen-4-one
IRISTECTORIGENINA
DTXSID30192285
HY-N2505
LMPK12050403
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Iristectorigenin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9440 94.40%
Caco-2 + 0.8824 88.24%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6642 66.42%
OATP2B1 inhibitior - 0.5653 56.53%
OATP1B1 inhibitior + 0.9574 95.74%
OATP1B3 inhibitior + 0.9261 92.61%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7074 70.74%
P-glycoprotein inhibitior - 0.5302 53.02%
P-glycoprotein substrate - 0.9188 91.88%
CYP3A4 substrate + 0.5479 54.79%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.7817 78.17%
CYP2C9 inhibition + 0.6258 62.58%
CYP2C19 inhibition + 0.8187 81.87%
CYP2D6 inhibition - 0.6249 62.49%
CYP1A2 inhibition + 0.8668 86.68%
CYP2C8 inhibition + 0.7313 73.13%
CYP inhibitory promiscuity + 0.8459 84.59%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6581 65.81%
Eye corrosion - 0.9779 97.79%
Eye irritation + 0.7296 72.96%
Skin irritation - 0.6522 65.22%
Skin corrosion - 0.9396 93.96%
Ames mutagenesis - 0.6982 69.82%
Human Ether-a-go-go-Related Gene inhibition - 0.7768 77.68%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.9222 92.22%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.6976 69.76%
Acute Oral Toxicity (c) III 0.5920 59.20%
Estrogen receptor binding + 0.9123 91.23%
Androgen receptor binding + 0.7769 77.69%
Thyroid receptor binding + 0.7052 70.52%
Glucocorticoid receptor binding + 0.8823 88.23%
Aromatase binding + 0.7677 76.77%
PPAR gamma + 0.8153 81.53%
Honey bee toxicity - 0.8413 84.13%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5351 53.51%
Fish aquatic toxicity + 0.8636 86.36%

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 98.12% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.30% 94.00%
CHEMBL2581 P07339 Cathepsin D 94.34% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.91% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.36% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.62% 89.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 90.07% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.21% 95.56%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 88.30% 80.78%
CHEMBL3194 P02766 Transthyretin 85.82% 90.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.55% 85.14%
CHEMBL3438 Q05513 Protein kinase C zeta 84.51% 88.48%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.20% 99.17%
CHEMBL4302 P08183 P-glycoprotein 1 83.79% 92.98%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.00% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.18% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 81.00% 93.31%
CHEMBL5903 Q04771 Activin receptor type-1 80.79% 89.93%

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.
Eriocaulon cinereum
Iris domestica
Iris florentina
Iris japonica
Iris pseudacorus
Iris spuria
Iris tectorum
Lantana camara
Sophora tomentosa

Cross-Links

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PubChem 5491637
NPASS NPC128513
LOTUS LTS0124153
wikiData Q83064938