Houttuynoside A

Details

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Internal ID 81092641-f2ae-4787-a79f-21187adeda84
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name methyl 4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(4-hydroxybenzoyl)oxymethyl]oxan-2-yl]oxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22O11/c1-29-19(27)11-4-7-13(23)14(8-11)31-21-18(26)17(25)16(24)15(32-21)9-30-20(28)10-2-5-12(22)6-3-10/h2-8,15-18,21-26H,9H2,1H3/t15-,16-,17+,18-,21-/m1/s1
InChI Key FBQCLBJQRYAZAQ-ZIKOTGLESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O11
Molecular Weight 450.40 g/mol
Exact Mass 450.11621151 g/mol
Topological Polar Surface Area (TPSA) 172.00 Ų
XlogP 0.60
Atomic LogP (AlogP) -0.07
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Houttuynoside A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7774 77.74%
Caco-2 - 0.8575 85.75%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6834 68.34%
OATP2B1 inhibitior - 0.7075 70.75%
OATP1B1 inhibitior + 0.8482 84.82%
OATP1B3 inhibitior + 0.9068 90.68%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.5572 55.72%
P-glycoprotein inhibitior - 0.5673 56.73%
P-glycoprotein substrate - 0.8280 82.80%
CYP3A4 substrate + 0.5629 56.29%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8530 85.30%
CYP3A4 inhibition - 0.8805 88.05%
CYP2C9 inhibition - 0.7954 79.54%
CYP2C19 inhibition - 0.8921 89.21%
CYP2D6 inhibition - 0.9291 92.91%
CYP1A2 inhibition - 0.8625 86.25%
CYP2C8 inhibition + 0.7380 73.80%
CYP inhibitory promiscuity - 0.8359 83.59%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7284 72.84%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.8514 85.14%
Skin irritation - 0.8516 85.16%
Skin corrosion - 0.9495 94.95%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3644 36.44%
Micronuclear + 0.6566 65.66%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.9221 92.21%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.7563 75.63%
Acute Oral Toxicity (c) III 0.8004 80.04%
Estrogen receptor binding + 0.5861 58.61%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5548 55.48%
Glucocorticoid receptor binding + 0.6466 64.66%
Aromatase binding - 0.6725 67.25%
PPAR gamma - 0.5631 56.31%
Honey bee toxicity - 0.9091 90.91%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.8066 80.66%
Fish aquatic toxicity + 0.8441 84.41%

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 98.07% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.79% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.54% 96.09%
CHEMBL4208 P20618 Proteasome component C5 91.46% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 89.68% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 88.28% 91.49%
CHEMBL3194 P02766 Transthyretin 87.87% 90.71%
CHEMBL2535 P11166 Glucose transporter 84.78% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.39% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.73% 94.00%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 83.40% 96.90%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 83.39% 95.83%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.17% 90.71%
CHEMBL4630 O14757 Serine/threonine-protein kinase Chk1 81.94% 97.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.76% 95.89%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.29% 89.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.80% 95.89%
CHEMBL2581 P07339 Cathepsin D 80.62% 98.95%
CHEMBL5255 O00206 Toll-like receptor 4 80.48% 92.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.26% 89.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.25% 94.33%

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.
Houttuynia cordata

Cross-Links

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PubChem 44521323
LOTUS LTS0232164
wikiData Q104992832