Theaflavate B

Details

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Internal ID 1ed27965-c396-4299-a6ac-1b7abaf68507
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Catechins
IUPAC Name [2-(3,4-dihydroxyphenyl)-6,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxy-6-oxo-1-(3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl)benzo[7]annulene-8-carboxylate
SMILES (Canonical) C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C4=C(C(=O)C=C(C=C34)C(=O)OC5CC6=CC(=C(C=C6OC5C7=CC(=C(C=C7)O)O)O)O)O)O)O)O
SMILES (Isomeric) C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C4=C(C(=O)C=C(C=C34)C(=O)OC5CC6=CC(=C(C=C6OC5C7=CC(=C(C=C7)O)O)O)O)O)O)O)O
InChI InChI=1S/C36H28O15/c37-16-8-21(39)19-11-27(45)35(50-29(19)9-16)18-10-26(44)33(47)31-17(18)3-15(6-25(43)32(31)46)36(48)51-30-7-14-5-23(41)24(42)12-28(14)49-34(30)13-1-2-20(38)22(40)4-13/h1-6,8-10,12,27,30,34-35,37-42,44-45,47H,7,11H2,(H,43,46)
InChI Key SEDUYIBVUMLAFJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C36H28O15
Molecular Weight 700.60 g/mol
Exact Mass 700.14282018 g/mol
Topological Polar Surface Area (TPSA) 264.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 15
H-Bond Donor 10
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Theaflavate B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5800 58.00%
Caco-2 - 0.9200 92.00%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.4676 46.76%
OATP2B1 inhibitior - 0.7051 70.51%
OATP1B1 inhibitior + 0.7430 74.30%
OATP1B3 inhibitior + 0.9683 96.83%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7783 77.83%
P-glycoprotein inhibitior + 0.7496 74.96%
P-glycoprotein substrate + 0.5139 51.39%
CYP3A4 substrate + 0.7110 71.10%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.7327 73.27%
CYP3A4 inhibition - 0.7575 75.75%
CYP2C9 inhibition - 0.9093 90.93%
CYP2C19 inhibition - 0.8777 87.77%
CYP2D6 inhibition - 0.9173 91.73%
CYP1A2 inhibition - 0.9401 94.01%
CYP2C8 inhibition + 0.8088 80.88%
CYP inhibitory promiscuity - 0.9660 96.60%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6324 63.24%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.8753 87.53%
Skin irritation - 0.7177 71.77%
Skin corrosion - 0.9351 93.51%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7716 77.16%
Micronuclear + 0.8459 84.59%
Hepatotoxicity - 0.5820 58.20%
skin sensitisation - 0.8838 88.38%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7767 77.67%
Acute Oral Toxicity (c) IV 0.3018 30.18%
Estrogen receptor binding + 0.7934 79.34%
Androgen receptor binding + 0.8355 83.55%
Thyroid receptor binding - 0.4898 48.98%
Glucocorticoid receptor binding + 0.5535 55.35%
Aromatase binding - 0.5794 57.94%
PPAR gamma + 0.6938 69.38%
Honey bee toxicity - 0.7052 70.52%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6350 63.50%
Fish aquatic toxicity + 0.9115 91.15%

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 99.92% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 99.87% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.45% 97.09%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 94.09% 83.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.45% 89.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 93.29% 96.12%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.14% 99.23%
CHEMBL2581 P07339 Cathepsin D 92.29% 98.95%
CHEMBL3194 P02766 Transthyretin 91.49% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.25% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.22% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.53% 93.99%
CHEMBL2535 P11166 Glucose transporter 90.48% 98.75%
CHEMBL4302 P08183 P-glycoprotein 1 90.48% 92.98%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.41% 95.56%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 89.20% 96.37%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.02% 99.15%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 87.73% 95.55%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 87.21% 92.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.52% 95.89%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 85.98% 95.64%
CHEMBL217 P14416 Dopamine D2 receptor 84.39% 95.62%
CHEMBL340 P08684 Cytochrome P450 3A4 83.90% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.49% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.26% 99.17%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 82.88% 95.78%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.85% 96.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.96% 100.00%
CHEMBL2056 P21728 Dopamine D1 receptor 80.63% 91.00%

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.
Camellia sinensis

Cross-Links

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PubChem 131751365
LOTUS LTS0030851
wikiData Q105251044