Bannamurpanisin

Details

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Internal ID a0576831-e04f-4e4d-81ee-1034d9df72e4
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 8-O-methylated flavonoids
IUPAC Name 5,7,8-trimethoxy-2-(3,4,5-trimethoxyphenyl)chromen-4-one
SMILES (Canonical) COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)OC
SMILES (Isomeric) COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(O2)C(=C(C=C3OC)OC)OC
InChI InChI=1S/C21H22O8/c1-23-14-10-17(26-4)20(28-6)21-18(14)12(22)9-13(29-21)11-7-15(24-2)19(27-5)16(8-11)25-3/h7-10H,1-6H3
InChI Key QLVJRZMVFHRFAV-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O8
Molecular Weight 402.40 g/mol
Exact Mass 402.13146766 g/mol
Topological Polar Surface Area (TPSA) 81.70 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.51
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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Compound NP-025444
SCHEMBL16894618
QLVJRZMVFHRFAV-UHFFFAOYSA-N
LMPK12111416
AKOS040736726
5,7,8,3',4',5'-hexamethoxyflavone
3',4',5',5,7,8-Hexamethoxyflavone
3',4',5,5',7,8-Hexamethoxyflavone
5,7,8-Trimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one #

2D Structure

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2D Structure of Bannamurpanisin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 + 0.8767 87.67%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7006 70.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9494 94.94%
OATP1B3 inhibitior + 0.9919 99.19%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7856 78.56%
P-glycoprotein inhibitior + 0.9322 93.22%
P-glycoprotein substrate - 0.8988 89.88%
CYP3A4 substrate - 0.5278 52.78%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7654 76.54%
CYP3A4 inhibition + 0.6138 61.38%
CYP2C9 inhibition - 0.7985 79.85%
CYP2C19 inhibition + 0.7445 74.45%
CYP2D6 inhibition - 0.9546 95.46%
CYP1A2 inhibition + 0.9694 96.94%
CYP2C8 inhibition + 0.4607 46.07%
CYP inhibitory promiscuity + 0.8123 81.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5636 56.36%
Eye corrosion - 0.9682 96.82%
Eye irritation + 0.5534 55.34%
Skin irritation - 0.7565 75.65%
Skin corrosion - 0.9845 98.45%
Ames mutagenesis - 0.5564 55.64%
Human Ether-a-go-go-Related Gene inhibition + 0.6566 65.66%
Micronuclear + 0.7759 77.59%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.9439 94.39%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6040 60.40%
Acute Oral Toxicity (c) II 0.6245 62.45%
Estrogen receptor binding + 0.9112 91.12%
Androgen receptor binding + 0.7173 71.73%
Thyroid receptor binding + 0.6482 64.82%
Glucocorticoid receptor binding + 0.7789 77.89%
Aromatase binding + 0.6947 69.47%
PPAR gamma + 0.7315 73.15%
Honey bee toxicity - 0.6805 68.05%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9192 91.92%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.45% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.60% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.44% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.25% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.73% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.31% 89.00%
CHEMBL2581 P07339 Cathepsin D 83.63% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.36% 99.17%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.82% 94.03%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.81% 93.99%
CHEMBL4302 P08183 P-glycoprotein 1 80.55% 92.98%

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.
Aniba burchellii
Murraya paniculata
Murraya paniculata
Neoraputia alba

Cross-Links

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PubChem 633619
NPASS NPC289882
LOTUS LTS0004529
wikiData Q104195951