Bis(3,4,5-trihydroxybenzoic acid)2alpha,2'alpha-bis(3,4-dihydroxyphenyl)-5,5',7,7'-tetrahydroxy-4,8'-bichroman-3alpha,3'alpha-diyl ester

Details

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Internal ID c9c3e34e-8f15-4098-8679-338f809e7837
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Biflavonoids and polyflavonoids
IUPAC Name [(2R,3R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxybenzoyl)oxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate
SMILES (Canonical) C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O
SMILES (Isomeric) C1[C@H]([C@H](OC2=C1C(=CC(=C2C3[C@H]([C@H](OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O
InChI InChI=1S/C44H34O20/c45-19-11-26(51)34-32(12-19)61-40(16-2-4-22(47)25(50)6-16)42(64-44(60)18-9-30(55)38(58)31(56)10-18)36(34)35-27(52)14-23(48)20-13-33(62-43(59)17-7-28(53)37(57)29(54)8-17)39(63-41(20)35)15-1-3-21(46)24(49)5-15/h1-12,14,33,36,39-40,42,45-58H,13H2/t33-,36?,39-,40-,42-/m1/s1
InChI Key KTLUHRSHFRODPS-ZMSZJQPBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C44H34O20
Molecular Weight 882.70 g/mol
Exact Mass 882.16434347 g/mol
Topological Polar Surface Area (TPSA) 354.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.96
H-Bond Acceptor 20
H-Bond Donor 14
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Bis(3,4,5-trihydroxybenzoic acid)2alpha,2'alpha-bis(3,4-dihydroxyphenyl)-5,5',7,7'-tetrahydroxy-4,8'-bichroman-3alpha,3'alpha-diyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7121 71.21%
Caco-2 - 0.8957 89.57%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6276 62.76%
OATP2B1 inhibitior - 0.8472 84.72%
OATP1B1 inhibitior + 0.8055 80.55%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8383 83.83%
P-glycoprotein inhibitior + 0.7327 73.27%
P-glycoprotein substrate - 0.6712 67.12%
CYP3A4 substrate + 0.6680 66.80%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.7271 72.71%
CYP3A4 inhibition - 0.8393 83.93%
CYP2C9 inhibition - 0.8024 80.24%
CYP2C19 inhibition - 0.8085 80.85%
CYP2D6 inhibition - 0.9646 96.46%
CYP1A2 inhibition - 0.9029 90.29%
CYP2C8 inhibition + 0.8133 81.33%
CYP inhibitory promiscuity - 0.9303 93.03%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6672 66.72%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.8841 88.41%
Skin irritation - 0.6964 69.64%
Skin corrosion - 0.9457 94.57%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7680 76.80%
Micronuclear + 0.8559 85.59%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8758 87.58%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7530 75.30%
Acute Oral Toxicity (c) IV 0.3575 35.75%
Estrogen receptor binding + 0.7760 77.60%
Androgen receptor binding + 0.8039 80.39%
Thyroid receptor binding + 0.5724 57.24%
Glucocorticoid receptor binding + 0.5592 55.92%
Aromatase binding - 0.5502 55.02%
PPAR gamma + 0.6944 69.44%
Honey bee toxicity - 0.7721 77.21%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9277 92.77%

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 99.57% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.97% 91.49%
CHEMBL3194 P02766 Transthyretin 95.34% 90.71%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 94.23% 83.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.50% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.13% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 91.02% 95.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.12% 86.33%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 89.36% 96.37%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.97% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.84% 99.17%
CHEMBL1929 P47989 Xanthine dehydrogenase 88.24% 96.12%
CHEMBL4208 P20618 Proteasome component C5 87.87% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.81% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.08% 99.15%
CHEMBL2581 P07339 Cathepsin D 83.54% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.45% 95.56%
CHEMBL245 P20309 Muscarinic acetylcholine receptor M3 82.89% 97.53%
CHEMBL4040 P28482 MAP kinase ERK2 82.66% 83.82%
CHEMBL233 P35372 Mu opioid receptor 82.57% 97.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.05% 95.89%
CHEMBL236 P41143 Delta opioid receptor 81.51% 99.35%
CHEMBL2535 P11166 Glucose transporter 81.14% 98.75%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 80.21% 95.78%

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.
Rheum officinale
Rheum palmatum
Rheum tanguticum

Cross-Links

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PubChem 12795894
NPASS NPC3415