Prestegane B

Details

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Internal ID 04d65d95-980a-4b15-8d60-aff022d685d1
Taxonomy Lignans, neolignans and related compounds > Furanoid lignans > Tetrahydrofuran lignans > 9,9-epoxylignans > Dibenzylbutyrolactone lignans
IUPAC Name (3R,4R)-3,4-bis[(3-hydroxy-4-methoxyphenyl)methyl]oxolan-2-one
SMILES (Canonical) COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC)O)O
SMILES (Isomeric) COC1=C(C=C(C=C1)C[C@H]2COC(=O)[C@@H]2CC3=CC(=C(C=C3)OC)O)O
InChI InChI=1S/C20H22O6/c1-24-18-5-3-12(9-16(18)21)7-14-11-26-20(23)15(14)8-13-4-6-19(25-2)17(22)10-13/h3-6,9-10,14-15,21-22H,7-8,11H2,1-2H3/t14-,15+/m0/s1
InChI Key IDASJTBLBSIWHG-LSDHHAIUSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H22O6
Molecular Weight 358.40 g/mol
Exact Mass 358.14163842 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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93376-04-6
Prestegane B - Hewittia subloblata
(3R,4R)-3,4-Bis(3-hydroxy-4-methoxybenzyl)dihydrofuran-2(3H)-one
(3R,4R)-3,4-bis[(3-hydroxy-4-methoxyphenyl)methyl]oxolan-2-one
SCHEMBL5853491
DTXSID50239404
NSC721156
NSC-721156
XP170500
2(3H)-Furanone, dihydro-3,4-bis((3-hydroxy-4-methoxyphenyl)methyl)-, (3R-trans)-

2D Structure

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2D Structure of Prestegane B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9224 92.24%
Caco-2 + 0.7255 72.55%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.9221 92.21%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9444 94.44%
OATP1B3 inhibitior + 0.8860 88.60%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8402 84.02%
P-glycoprotein inhibitior + 0.6004 60.04%
P-glycoprotein substrate - 0.7846 78.46%
CYP3A4 substrate - 0.5229 52.29%
CYP2C9 substrate - 0.5898 58.98%
CYP2D6 substrate - 0.7380 73.80%
CYP3A4 inhibition + 0.7912 79.12%
CYP2C9 inhibition + 0.9043 90.43%
CYP2C19 inhibition + 0.8936 89.36%
CYP2D6 inhibition - 0.7980 79.80%
CYP1A2 inhibition + 0.8318 83.18%
CYP2C8 inhibition - 0.7134 71.34%
CYP inhibitory promiscuity + 0.9049 90.49%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8617 86.17%
Carcinogenicity (trinary) Non-required 0.6394 63.94%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.5102 51.02%
Skin irritation - 0.8419 84.19%
Skin corrosion - 0.9738 97.38%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6534 65.34%
Micronuclear + 0.5292 52.92%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.8770 87.70%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6423 64.23%
Acute Oral Toxicity (c) III 0.6295 62.95%
Estrogen receptor binding + 0.7792 77.92%
Androgen receptor binding + 0.7489 74.89%
Thyroid receptor binding + 0.5737 57.37%
Glucocorticoid receptor binding + 0.6523 65.23%
Aromatase binding - 0.5477 54.77%
PPAR gamma + 0.5633 56.33%
Honey bee toxicity - 0.8588 85.88%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity + 0.9918 99.18%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.17% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.68% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 95.51% 83.82%
CHEMBL2581 P07339 Cathepsin D 94.57% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.43% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.31% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.03% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.14% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.13% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.79% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.43% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.59% 95.89%
CHEMBL1255126 O15151 Protein Mdm4 82.45% 90.20%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.10% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.54% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.53% 85.14%
CHEMBL2535 P11166 Glucose transporter 80.49% 98.75%
CHEMBL261 P00915 Carbonic anhydrase I 80.48% 96.76%
CHEMBL3401 O75469 Pregnane X receptor 80.30% 94.73%

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.
Spatholobus suberectus
Steganotaenia araliacea

Cross-Links

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PubChem 146425
NPASS NPC122371
LOTUS LTS0092537
wikiData Q83121760