Phyllanemblinin B

Details

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Internal ID b2c72509-ae83-4c17-994a-72dd0f9bd266
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name [(1S,18R,19S,21R,22S)-6,7,8,11,12,13,22-heptahydroxy-21-(hydroxymethyl)-3,16-dioxo-2,17,20-trioxatetracyclo[16.3.1.04,9.010,15]docosa-4,6,8,10,12,14-hexaen-19-yl] 3,4,5-trihydroxybenzoate
SMILES (Canonical) C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)O
SMILES (Isomeric) C1=C(C=C(C(=C1O)O)O)C(=O)O[C@H]2[C@H]3[C@H]([C@@H]([C@H](O2)CO)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)O
InChI InChI=1S/C27H22O18/c28-5-13-22-21(38)23(27(42-13)45-24(39)6-1-9(29)16(33)10(30)2-6)44-26(41)8-4-12(32)18(35)20(37)15(8)14-7(25(40)43-22)3-11(31)17(34)19(14)36/h1-4,13,21-23,27-38H,5H2/t13-,21+,22-,23-,27+/m1/s1
InChI Key NJXCTOMVEYVVGG-MLKBLKPTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H22O18
Molecular Weight 634.50 g/mol
Exact Mass 634.08061385 g/mol
Topological Polar Surface Area (TPSA) 311.00 Ų
XlogP 0.10
Atomic LogP (AlogP) -0.30
H-Bond Acceptor 18
H-Bond Donor 11
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Phyllanemblinin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7085 70.85%
Caco-2 - 0.9047 90.47%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5238 52.38%
OATP2B1 inhibitior - 0.5572 55.72%
OATP1B1 inhibitior - 0.4351 43.51%
OATP1B3 inhibitior + 0.9534 95.34%
MATE1 inhibitior - 0.5600 56.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6153 61.53%
P-glycoprotein inhibitior + 0.6446 64.46%
P-glycoprotein substrate - 0.8770 87.70%
CYP3A4 substrate + 0.5680 56.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8401 84.01%
CYP3A4 inhibition - 0.8527 85.27%
CYP2C9 inhibition - 0.8589 85.89%
CYP2C19 inhibition - 0.9055 90.55%
CYP2D6 inhibition - 0.9340 93.40%
CYP1A2 inhibition - 0.9278 92.78%
CYP2C8 inhibition + 0.4669 46.69%
CYP inhibitory promiscuity - 0.8555 85.55%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7196 71.96%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.8336 83.36%
Skin irritation - 0.8214 82.14%
Skin corrosion - 0.9642 96.42%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8261 82.61%
Micronuclear + 0.6233 62.33%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation - 0.8793 87.93%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8329 83.29%
Acute Oral Toxicity (c) III 0.4262 42.62%
Estrogen receptor binding + 0.7692 76.92%
Androgen receptor binding + 0.6598 65.98%
Thyroid receptor binding - 0.5498 54.98%
Glucocorticoid receptor binding - 0.5313 53.13%
Aromatase binding - 0.6035 60.35%
PPAR gamma + 0.6587 65.87%
Honey bee toxicity - 0.8190 81.90%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5950 59.50%
Fish aquatic toxicity + 0.8241 82.41%

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 99.40% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.10% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.79% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.46% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 89.35% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.17% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.03% 86.33%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 88.48% 83.00%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 88.19% 95.64%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.91% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 87.69% 94.73%
CHEMBL3194 P02766 Transthyretin 87.22% 90.71%
CHEMBL1951 P21397 Monoamine oxidase A 86.14% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.32% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.38% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.26% 99.15%

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.
Phyllanthus emblica

Cross-Links

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PubChem 10941235
NPASS NPC29310
LOTUS LTS0126399
wikiData Q105180355