Peperphilippinin III

Details

Top
Internal ID 8eebb6ba-e32b-4c09-b4f4-89fcd6f6315e
Taxonomy Lignans, neolignans and related compounds > Furanoid lignans > Tetrahydrofuran lignans > 9,9-epoxylignans > Dibenzylbutyrolactone lignans
IUPAC Name (3E,4R)-3-[(4-hydroxy-3,5-dimethoxyphenyl)methylidene]-4-[(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one
SMILES (Canonical) COC1=CC(=CC(=C1OC)OC)CC2COC(=O)C2=CC3=CC(=C(C(=C3)OC)O)OC
SMILES (Isomeric) COC1=CC(=CC(=C1OC)OC)C[C@H]\2COC(=O)/C2=C/C3=CC(=C(C(=C3)OC)O)OC
InChI InChI=1S/C23H26O8/c1-26-17-8-14(9-18(27-2)21(17)24)7-16-15(12-31-23(16)25)6-13-10-19(28-3)22(30-5)20(11-13)29-4/h7-11,15,24H,6,12H2,1-5H3/b16-7+/t15-/m0/s1
InChI Key CZLLEPKEWJTTCK-PLWLOYALSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C23H26O8
Molecular Weight 430.40 g/mol
Exact Mass 430.16276778 g/mol
Topological Polar Surface Area (TPSA) 92.70 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Peperphilippinin III

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9854 98.54%
Caco-2 + 0.6811 68.11%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8218 82.18%
OATP2B1 inhibitior - 0.8649 86.49%
OATP1B1 inhibitior + 0.8875 88.75%
OATP1B3 inhibitior + 0.9121 91.21%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8154 81.54%
P-glycoprotein inhibitior + 0.7364 73.64%
P-glycoprotein substrate - 0.6891 68.91%
CYP3A4 substrate + 0.5996 59.96%
CYP2C9 substrate + 0.5928 59.28%
CYP2D6 substrate - 0.7807 78.07%
CYP3A4 inhibition + 0.5416 54.16%
CYP2C9 inhibition + 0.6683 66.83%
CYP2C19 inhibition + 0.9099 90.99%
CYP2D6 inhibition - 0.8759 87.59%
CYP1A2 inhibition + 0.7964 79.64%
CYP2C8 inhibition + 0.6649 66.49%
CYP inhibitory promiscuity + 0.9286 92.86%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9228 92.28%
Carcinogenicity (trinary) Non-required 0.5392 53.92%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.8363 83.63%
Skin irritation - 0.8179 81.79%
Skin corrosion - 0.9833 98.33%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4215 42.15%
Micronuclear + 0.7066 70.66%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.7360 73.60%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.7583 75.83%
Acute Oral Toxicity (c) III 0.4983 49.83%
Estrogen receptor binding + 0.9119 91.19%
Androgen receptor binding - 0.5512 55.12%
Thyroid receptor binding + 0.7785 77.85%
Glucocorticoid receptor binding + 0.8336 83.36%
Aromatase binding - 0.4893 48.93%
PPAR gamma + 0.7933 79.33%
Honey bee toxicity - 0.8264 82.64%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9884 98.84%

Targets

Top

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 98.73% 91.11%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 95.16% 83.57%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.06% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.31% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.13% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.84% 96.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 92.79% 92.62%
CHEMBL2581 P07339 Cathepsin D 92.73% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.86% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.16% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.89% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.92% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.46% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 82.99% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.62% 96.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.14% 89.34%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.17% 94.00%

Plants that contains it

Top
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

Top
PubChem 17754952
NPASS NPC299909
LOTUS LTS0251840
wikiData Q104972871