Corymbosin

Details

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Internal ID 2e8be5b9-4b41-4011-982c-c24369edc074
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name 5-hydroxy-7-methoxy-2-(3,4,5-trimethoxyphenyl)chromen-4-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3)OC)OC)OC)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3)OC)OC)OC)O
InChI InChI=1S/C19H18O7/c1-22-11-7-12(20)18-13(21)9-14(26-15(18)8-11)10-5-16(23-2)19(25-4)17(6-10)24-3/h5-9,20H,1-4H3
InChI Key FLCVGMVLNHYJAW-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O7
Molecular Weight 358.30 g/mol
Exact Mass 358.10525291 g/mol
Topological Polar Surface Area (TPSA) 83.40 Ų
XlogP 2.30
Atomic LogP (AlogP) 3.20
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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18103-41-8
5-hydroxy-7-methoxy-2-(3,4,5-trimethoxyphenyl)chromen-4-one
5-Hydroxy-3',4',5',7-tetramethoxyflavone
2-(3,4,5-Trimethoxyphenyl)-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one
CHEMBL511257
SCHEMBL1976826
FLCVGMVLNHYJAW-UHFFFAOYSA-N
DTXSID701347298
HY-N7329
LMPK12111069
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Corymbosin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.9010 90.10%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7745 77.45%
OATP2B1 inhibitior - 0.8645 86.45%
OATP1B1 inhibitior + 0.9503 95.03%
OATP1B3 inhibitior + 0.9817 98.17%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5584 55.84%
P-glycoprotein inhibitior + 0.9124 91.24%
P-glycoprotein substrate - 0.8971 89.71%
CYP3A4 substrate + 0.5076 50.76%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition - 0.5748 57.48%
CYP2C9 inhibition - 0.8861 88.61%
CYP2C19 inhibition + 0.5778 57.78%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition + 0.8530 85.30%
CYP2C8 inhibition + 0.6910 69.10%
CYP inhibitory promiscuity + 0.6103 61.03%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5716 57.16%
Eye corrosion - 0.9793 97.93%
Eye irritation - 0.5236 52.36%
Skin irritation - 0.7150 71.50%
Skin corrosion - 0.9836 98.36%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4532 45.32%
Micronuclear + 0.8359 83.59%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.9504 95.04%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6626 66.26%
Acute Oral Toxicity (c) II 0.4982 49.82%
Estrogen receptor binding + 0.9323 93.23%
Androgen receptor binding + 0.6868 68.68%
Thyroid receptor binding + 0.7079 70.79%
Glucocorticoid receptor binding + 0.7953 79.53%
Aromatase binding + 0.7239 72.39%
PPAR gamma + 0.8017 80.17%
Honey bee toxicity - 0.8015 80.15%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity + 0.8902 89.02%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.59% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.82% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.38% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.37% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.40% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.83% 89.00%
CHEMBL3194 P02766 Transthyretin 89.46% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.40% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.37% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.52% 93.99%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.37% 95.50%
CHEMBL4208 P20618 Proteasome component C5 81.38% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.04% 99.23%
CHEMBL2581 P07339 Cathepsin D 80.97% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 80.68% 94.73%

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.
Arctotis argentea
Ballota glandulosissima
Gardenia jasminoides
Lethedon tannensis

Cross-Links

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PubChem 10970376
NPASS NPC33265
LOTUS LTS0007504
wikiData Q63392823