Hemiariensin

Details

Top
Internal ID 3e8c7cd2-b8d5-4c69-92a0-07861e4c58f9
Taxonomy Lignans, neolignans and related compounds > Dibenzylbutane lignans
IUPAC Name [2,3-bis(1,3-benzodioxol-5-ylmethyl)-4-hydroxybutyl] acetate
SMILES (Canonical) CC(=O)OCC(CC1=CC2=C(C=C1)OCO2)C(CC3=CC4=C(C=C3)OCO4)CO
SMILES (Isomeric) CC(=O)OCC(CC1=CC2=C(C=C1)OCO2)C(CC3=CC4=C(C=C3)OCO4)CO
InChI InChI=1S/C22H24O7/c1-14(24)25-11-18(7-16-3-5-20-22(9-16)29-13-27-20)17(10-23)6-15-2-4-19-21(8-15)28-12-26-19/h2-5,8-9,17-18,23H,6-7,10-13H2,1H3
InChI Key ZSECDNBADLTTJC-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C22H24O7
Molecular Weight 400.40 g/mol
Exact Mass 400.15220310 g/mol
Topological Polar Surface Area (TPSA) 83.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

Top
SCHEMBL29477360
CHEBI:172639
[2,3-bis(1,3-benzodioxol-5-ylmethyl)-4-hydroxybutyl] acetate

2D Structure

Top
2D Structure of Hemiariensin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9797 97.97%
Caco-2 + 0.5200 52.00%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7646 76.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9361 93.61%
OATP1B3 inhibitior + 0.9516 95.16%
MATE1 inhibitior - 0.9412 94.12%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9785 97.85%
P-glycoprotein inhibitior + 0.7528 75.28%
P-glycoprotein substrate - 0.9010 90.10%
CYP3A4 substrate - 0.5520 55.20%
CYP2C9 substrate - 0.5986 59.86%
CYP2D6 substrate - 0.8390 83.90%
CYP3A4 inhibition + 0.7041 70.41%
CYP2C9 inhibition + 0.7536 75.36%
CYP2C19 inhibition + 0.7945 79.45%
CYP2D6 inhibition - 0.6780 67.80%
CYP1A2 inhibition + 0.7553 75.53%
CYP2C8 inhibition - 0.9018 90.18%
CYP inhibitory promiscuity + 0.7916 79.16%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.4760 47.60%
Eye corrosion - 0.9830 98.30%
Eye irritation - 0.8848 88.48%
Skin irritation - 0.7130 71.30%
Skin corrosion - 0.9329 93.29%
Ames mutagenesis - 0.6744 67.44%
Human Ether-a-go-go-Related Gene inhibition + 0.7633 76.33%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.5196 51.96%
skin sensitisation - 0.7498 74.98%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6421 64.21%
Acute Oral Toxicity (c) III 0.6953 69.53%
Estrogen receptor binding + 0.8439 84.39%
Androgen receptor binding + 0.7701 77.01%
Thyroid receptor binding + 0.5835 58.35%
Glucocorticoid receptor binding + 0.6767 67.67%
Aromatase binding - 0.5454 54.54%
PPAR gamma - 0.4836 48.36%
Honey bee toxicity - 0.8849 88.49%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7255 72.55%
Fish aquatic toxicity + 0.9825 98.25%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.94% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.27% 96.77%
CHEMBL2581 P07339 Cathepsin D 96.50% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.10% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.55% 91.11%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 91.19% 94.80%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.67% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.22% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.91% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 87.49% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.80% 95.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.93% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.69% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.10% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.03% 96.00%

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.
There are no matching plants.

Cross-Links

Top
PubChem 13939341
LOTUS LTS0003825
wikiData Q105382471