Isotectorigenin

Details

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Internal ID 3dd68d4e-77ff-4885-b05d-dc1c28c0f025
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 5,7-dihydroxy-3-(4-hydroxyphenyl)-8-methoxychromen-4-one
SMILES (Canonical) COC1=C(C=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)O
SMILES (Isomeric) COC1=C(C=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)O
InChI InChI=1S/C16H12O6/c1-21-15-12(19)6-11(18)13-14(20)10(7-22-16(13)15)8-2-4-9(17)5-3-8/h2-7,17-19H,1H3
InChI Key UYLQOGTYNFVQQX-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O6
Molecular Weight 300.26 g/mol
Exact Mass 300.06338810 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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Isotectorigenin
13111-57-4
Pseudotectorigenin
5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-methoxy-4H-chromen-4-one
5,7-dihydroxy-3-(4-hydroxyphenyl)-8-methoxychromen-4-one
UNII-8HXB4THX7F
8HXB4THX7F
5,7,4'-Trihydroxy-8-methoxyisoflavone
BRN 0305254
5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-methoxy-4H-1-benzopyran-4-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isotectorigenin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9524 95.24%
Caco-2 + 0.9000 90.00%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6494 64.94%
OATP2B1 inhibitior + 0.5574 55.74%
OATP1B1 inhibitior + 0.9261 92.61%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6910 69.10%
P-glycoprotein inhibitior - 0.7606 76.06%
P-glycoprotein substrate - 0.9344 93.44%
CYP3A4 substrate + 0.5202 52.02%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.7348 73.48%
CYP2C9 inhibition + 0.7560 75.60%
CYP2C19 inhibition + 0.8648 86.48%
CYP2D6 inhibition - 0.6993 69.93%
CYP1A2 inhibition + 0.9218 92.18%
CYP2C8 inhibition + 0.6240 62.40%
CYP inhibitory promiscuity + 0.8546 85.46%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6176 61.76%
Eye corrosion - 0.9767 97.67%
Eye irritation + 0.9127 91.27%
Skin irritation - 0.5841 58.41%
Skin corrosion - 0.9319 93.19%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7020 70.20%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.9240 92.40%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.4665 46.65%
Acute Oral Toxicity (c) III 0.7362 73.62%
Estrogen receptor binding + 0.9091 90.91%
Androgen receptor binding + 0.8793 87.93%
Thyroid receptor binding + 0.7944 79.44%
Glucocorticoid receptor binding + 0.8837 88.37%
Aromatase binding + 0.7112 71.12%
PPAR gamma + 0.7725 77.25%
Honey bee toxicity - 0.8971 89.71%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8321 83.21%

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 97.38% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.06% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.82% 94.00%
CHEMBL242 Q92731 Estrogen receptor beta 93.83% 98.35%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.73% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.69% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.11% 89.00%
CHEMBL3194 P02766 Transthyretin 86.86% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.95% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.16% 86.92%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.65% 95.56%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.16% 91.71%
CHEMBL1937 Q92769 Histone deacetylase 2 80.02% 94.75%

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.
Iris domestica
Iris tectorum

Cross-Links

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PubChem 5353911
NPASS NPC131266
LOTUS LTS0011600
wikiData Q3409943