Peperphilippinin VI

Details

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Internal ID f60aa901-74d5-4697-bf1e-576f74339d45
Taxonomy Lignans, neolignans and related compounds > Dibenzylbutane lignans > Dibenzylbutanediol lignans
IUPAC Name (2R,3R)-2-(1,3-benzodioxol-5-ylmethyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]butane-1,4-diol
SMILES (Canonical) COC1=C(C=CC(=C1)CC(CO)C(CC2=CC3=C(C=C2)OCO3)CO)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C[C@@H](CO)[C@@H](CC2=CC3=C(C=C2)OCO3)CO)O
InChI InChI=1S/C20H24O6/c1-24-19-8-13(2-4-17(19)23)6-15(10-21)16(11-22)7-14-3-5-18-20(9-14)26-12-25-18/h2-5,8-9,15-16,21-23H,6-7,10-12H2,1H3/t15-,16-/m0/s1
InChI Key DHCLUBMQECJTCD-HOTGVXAUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O6
Molecular Weight 360.40 g/mol
Exact Mass 360.15728848 g/mol
Topological Polar Surface Area (TPSA) 88.40 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.13
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Peperphilippinin VI

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9252 92.52%
Caco-2 + 0.5226 52.26%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.7322 73.22%
OATP2B1 inhibitior - 0.8605 86.05%
OATP1B1 inhibitior + 0.9203 92.03%
OATP1B3 inhibitior + 0.9617 96.17%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7848 78.48%
P-glycoprotein inhibitior - 0.4553 45.53%
P-glycoprotein substrate - 0.8616 86.16%
CYP3A4 substrate - 0.5395 53.95%
CYP2C9 substrate - 0.8108 81.08%
CYP2D6 substrate + 0.3952 39.52%
CYP3A4 inhibition + 0.8135 81.35%
CYP2C9 inhibition + 0.7356 73.56%
CYP2C19 inhibition + 0.8211 82.11%
CYP2D6 inhibition - 0.5585 55.85%
CYP1A2 inhibition + 0.5290 52.90%
CYP2C8 inhibition - 0.5646 56.46%
CYP inhibitory promiscuity + 0.8869 88.69%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.3819 38.19%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.8387 83.87%
Skin irritation - 0.7542 75.42%
Skin corrosion - 0.9406 94.06%
Ames mutagenesis - 0.6644 66.44%
Human Ether-a-go-go-Related Gene inhibition + 0.7597 75.97%
Micronuclear + 0.6700 67.00%
Hepatotoxicity - 0.5696 56.96%
skin sensitisation - 0.8156 81.56%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7465 74.65%
Acute Oral Toxicity (c) III 0.6671 66.71%
Estrogen receptor binding + 0.8366 83.66%
Androgen receptor binding + 0.7944 79.44%
Thyroid receptor binding + 0.5952 59.52%
Glucocorticoid receptor binding - 0.4896 48.96%
Aromatase binding - 0.5298 52.98%
PPAR gamma + 0.6608 66.08%
Honey bee toxicity - 0.8757 87.57%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5349 53.49%
Fish aquatic toxicity + 0.9365 93.65%

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 98.35% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.74% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.82% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.19% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 93.97% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.28% 96.77%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.38% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.18% 86.33%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.66% 90.24%
CHEMBL1255126 O15151 Protein Mdm4 87.44% 90.20%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.95% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.48% 95.56%
CHEMBL2535 P11166 Glucose transporter 86.15% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.55% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.40% 89.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.27% 99.15%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.31% 95.50%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.04% 95.17%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 82.11% 82.67%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 80.86% 93.24%
CHEMBL4208 P20618 Proteasome component C5 80.52% 90.00%

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.
Asplenium adiantum-nigrum
Distemonanthus benthamianus
Piper kwashoense

Cross-Links

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PubChem 17754956
NPASS NPC244136
LOTUS LTS0013696
wikiData Q104979841