beta-Peltatin-beta-D-glucoside

Details

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Internal ID 0f97eae4-a800-4da5-a2ba-8e5fe6923811
Taxonomy Lignans, neolignans and related compounds > Lignan glycosides
IUPAC Name (5aR,8aR,9R)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one
SMILES (Canonical) COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O)COC3=O
SMILES (Isomeric) COC1=CC(=CC(=C1OC)OC)[C@H]2[C@@H]3[C@@H](CC4=C(C5=C(C=C24)OCO5)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)COC3=O
InChI InChI=1S/C28H32O13/c1-34-15-5-11(6-16(35-2)25(15)36-3)19-13-7-17-26(39-10-38-17)24(14(13)4-12-9-37-27(33)20(12)19)41-28-23(32)22(31)21(30)18(8-29)40-28/h5-7,12,18-23,28-32H,4,8-10H2,1-3H3/t12-,18+,19+,20-,21+,22-,23+,28-/m0/s1
InChI Key PAIASCMUTMHGHU-WELBBKRVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C28H32O13
Molecular Weight 576.50 g/mol
Exact Mass 576.18429107 g/mol
Topological Polar Surface Area (TPSA) 172.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.10
H-Bond Acceptor 13
H-Bond Donor 4
Rotatable Bonds 7

Synonyms

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NSC-163025
UNII-1673AQJ022
beta-Peltatin-beta-D-glucoside [MI]
1673AQJ022
beta-Peltatin-o-beta-D-glucopyranoside
beta-Peltatin-beta-D-glucoside, (-)-
(-)-beta-Peltatin-5-o-beta-D-glucopyranoside
(-)-|A-Peltatin-5-O-beta-D-glucopyranoside
11024-59-2
Furo(3',4':6,7)naphtho(2,3-d)-1,3-dioxol-6(5ah)-one, 10-(beta-D-glucopyranosyloxy)-5,8,8a,9-tetrahydro-5-(3,4,5-trimethoxyphenyl)-, (5R,5aR,8aR)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of beta-Peltatin-beta-D-glucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5948 59.48%
Caco-2 - 0.8098 80.98%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6138 61.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8981 89.81%
OATP1B3 inhibitior + 0.9617 96.17%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8466 84.66%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.6466 64.66%
CYP3A4 substrate + 0.6786 67.86%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8419 84.19%
CYP3A4 inhibition - 0.6952 69.52%
CYP2C9 inhibition - 0.8203 82.03%
CYP2C19 inhibition - 0.7727 77.27%
CYP2D6 inhibition - 0.9178 91.78%
CYP1A2 inhibition - 0.9313 93.13%
CYP2C8 inhibition + 0.5748 57.48%
CYP inhibitory promiscuity + 0.6031 60.31%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5937 59.37%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9413 94.13%
Skin irritation - 0.8298 82.98%
Skin corrosion - 0.9519 95.19%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4418 44.18%
Micronuclear + 0.6933 69.33%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.8894 88.94%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.6458 64.58%
Acute Oral Toxicity (c) III 0.7638 76.38%
Estrogen receptor binding + 0.8520 85.20%
Androgen receptor binding + 0.6647 66.47%
Thyroid receptor binding + 0.5274 52.74%
Glucocorticoid receptor binding + 0.6470 64.70%
Aromatase binding - 0.5388 53.88%
PPAR gamma + 0.6600 66.00%
Honey bee toxicity - 0.6718 67.18%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.7723 77.23%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.72% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.18% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.56% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.42% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 93.49% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.97% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.44% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.03% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.54% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.59% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.56% 96.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.33% 96.77%
CHEMBL4040 P28482 MAP kinase ERK2 88.07% 83.82%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.67% 94.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 86.52% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.21% 95.89%
CHEMBL2535 P11166 Glucose transporter 83.34% 98.75%
CHEMBL4208 P20618 Proteasome component C5 83.29% 90.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.10% 97.25%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 82.77% 82.67%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.75% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 82.31% 94.73%
CHEMBL220 P22303 Acetylcholinesterase 81.68% 94.45%

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.
Bridelia ferruginea
Bursera simaruba
Podophyllum peltatum

Cross-Links

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PubChem 6325789
NPASS NPC222531
LOTUS LTS0143463
wikiData Q27251786