Calycopterin

Details

Top
Internal ID ebd4a08e-7a40-4073-8878-345a0424cba1
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 8-O-methylated flavonoids
IUPAC Name 5-hydroxy-2-(4-hydroxyphenyl)-3,6,7,8-tetramethoxychromen-4-one
SMILES (Canonical) COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)OC
SMILES (Isomeric) COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)OC
InChI InChI=1S/C19H18O8/c1-23-16-12(21)11-13(22)17(24-2)19(26-4)18(25-3)15(11)27-14(16)9-5-7-10(20)8-6-9/h5-8,20,22H,1-4H3
InChI Key PIUSRRUXGNYCSS-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H18O8
Molecular Weight 374.30 g/mol
Exact Mass 374.10016753 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.91
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

Top
481-52-7
Calcycopterin
5,4'-Dihydroxy-3,6,7,8-tetramethoxyflavone
8794DO3YB5
UNII-8794DO3YB5
5-hydroxy-2-(4-hydroxyphenyl)-3,6,7,8-tetramethoxychromen-4-one
4H-1-Benzopyran-4-one, 5-hydroxy-2-(4-hydroxyphenyl)-3,6,7,8-tetramethoxy-
Thapsin
CHEMBL512767
SCHEMBL2214965
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Calycopterin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9711 97.11%
Caco-2 + 0.6832 68.32%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7936 79.36%
OATP2B1 inhibitior - 0.7154 71.54%
OATP1B1 inhibitior + 0.8917 89.17%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.4506 45.06%
P-glycoprotein inhibitior + 0.7722 77.22%
P-glycoprotein substrate - 0.8590 85.90%
CYP3A4 substrate - 0.5082 50.82%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.7237 72.37%
CYP2C9 inhibition - 0.6863 68.63%
CYP2C19 inhibition + 0.6566 65.66%
CYP2D6 inhibition - 0.8329 83.29%
CYP1A2 inhibition + 0.8642 86.42%
CYP2C8 inhibition + 0.7310 73.10%
CYP inhibitory promiscuity + 0.7231 72.31%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5851 58.51%
Eye corrosion - 0.9825 98.25%
Eye irritation + 0.6337 63.37%
Skin irritation - 0.7275 72.75%
Skin corrosion - 0.9759 97.59%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5530 55.30%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.5176 51.76%
skin sensitisation - 0.9511 95.11%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5189 51.89%
Acute Oral Toxicity (c) III 0.4741 47.41%
Estrogen receptor binding + 0.8021 80.21%
Androgen receptor binding + 0.7865 78.65%
Thyroid receptor binding + 0.6851 68.51%
Glucocorticoid receptor binding + 0.8150 81.50%
Aromatase binding + 0.6301 63.01%
PPAR gamma + 0.7617 76.17%
Honey bee toxicity - 0.8927 89.27%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8969 89.69%

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 97.64% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.65% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.10% 94.45%
CHEMBL2581 P07339 Cathepsin D 92.43% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.31% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.59% 86.33%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 88.45% 95.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.15% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 84.76% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.45% 99.23%

Cross-Links

Top
PubChem 10429470
NPASS NPC105242
LOTUS LTS0003876
wikiData Q27269811