5,2',3'-Trihydroxy-6,7-Methylenedioxyflavanone

Details

Top
Internal ID 08a09f13-0fd7-4375-864b-3922dbb86e91
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Flavanones
IUPAC Name 6-(2,3-dihydroxyphenyl)-9-hydroxy-6,7-dihydro-[1,3]dioxolo[4,5-g]chromen-8-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H12O7/c17-8-3-1-2-7(14(8)19)10-4-9(18)13-11(23-10)5-12-16(15(13)20)22-6-21-12/h1-3,5,10,17,19-20H,4,6H2
InChI Key KGKAAUBCGDPTDT-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C16H12O7
Molecular Weight 316.26 g/mol
Exact Mass 316.05830272 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.24
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

Top
6-(2,3-dihydroxyphenyl)-9-hydroxy-6,7-dihydro-[1,3]dioxolo[4,5-g]chromen-8-one
6-(2,3-dihydroxyphenyl)-9-hydroxy-6,7-dihydro-(1,3)dioxolo(4,5-g)chromen-8-one
RefChem:100942
188440-64-4
CHEMBL1807889
SCHEMBL28031092
CHEBI:186862
LMPK12140603

2D Structure

Top
2D Structure of 5,2',3'-Trihydroxy-6,7-Methylenedioxyflavanone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8970 89.70%
Caco-2 - 0.8243 82.43%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8201 82.01%
OATP2B1 inhibitior - 0.7064 70.64%
OATP1B1 inhibitior + 0.9318 93.18%
OATP1B3 inhibitior + 0.9414 94.14%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6530 65.30%
P-glycoprotein inhibitior - 0.8210 82.10%
P-glycoprotein substrate - 0.8523 85.23%
CYP3A4 substrate + 0.5355 53.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8009 80.09%
CYP3A4 inhibition - 0.6080 60.80%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition - 0.6561 65.61%
CYP2D6 inhibition - 0.7087 70.87%
CYP1A2 inhibition - 0.6282 62.82%
CYP2C8 inhibition - 0.6386 63.86%
CYP inhibitory promiscuity - 0.6391 63.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5273 52.73%
Eye corrosion - 0.9916 99.16%
Eye irritation + 0.8373 83.73%
Skin irritation - 0.7098 70.98%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7737 77.37%
Micronuclear + 0.8233 82.33%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation - 0.8420 84.20%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.5591 55.91%
Acute Oral Toxicity (c) III 0.4546 45.46%
Estrogen receptor binding + 0.7806 78.06%
Androgen receptor binding + 0.6085 60.85%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7503 75.03%
Aromatase binding + 0.5711 57.11%
PPAR gamma + 0.8090 80.90%
Honey bee toxicity - 0.8553 85.53%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9148 91.48%

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 99.37% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.53% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.95% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 92.21% 93.40%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.55% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.24% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.11% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.65% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.18% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.67% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.61% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.07% 94.80%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 85.32% 81.29%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.00% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.66% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.25% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.56% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.34% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 81.29% 94.73%
CHEMBL2535 P11166 Glucose transporter 81.06% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.53% 96.09%

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 tenuifolia

Cross-Links

Top
PubChem 42608091
LOTUS LTS0132759
wikiData Q105140814