Asteltoxin D

Details

Top
Internal ID 420cd6ba-8ae5-4119-8147-286574fd682a
Taxonomy Organoheterocyclic compounds > Furofurans
IUPAC Name 6-[(1E,3E)-4-[(1R,2R,4R,5R,6R,8S,10R,11R)-5,11-dihydroxy-1,10,11-trimethyl-3,7,9-trioxatricyclo[6.3.0.02,6]undecan-4-yl]buta-1,3-dienyl]-4-methoxy-5-methylpyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H28O8/c1-11-13(28-16(23)10-15(11)26-5)8-6-7-9-14-17(24)18-19(29-14)21(3)20(30-18)27-12(2)22(21,4)25/h6-10,12,14,17-20,24-25H,1-5H3/b8-6+,9-7+/t12-,14-,17-,18-,19+,20-,21+,22+/m1/s1
InChI Key AVOLRKQPXXFPLF-WMBDBGTCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C22H28O8
Molecular Weight 420.50 g/mol
Exact Mass 420.17841785 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.56
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Asteltoxin D

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9659 96.59%
Caco-2 - 0.7163 71.63%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6965 69.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8717 87.17%
OATP1B3 inhibitior + 0.9073 90.73%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7178 71.78%
P-glycoprotein inhibitior - 0.4746 47.46%
P-glycoprotein substrate - 0.5303 53.03%
CYP3A4 substrate + 0.6706 67.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8652 86.52%
CYP3A4 inhibition - 0.5774 57.74%
CYP2C9 inhibition - 0.9127 91.27%
CYP2C19 inhibition - 0.6312 63.12%
CYP2D6 inhibition - 0.8267 82.67%
CYP1A2 inhibition - 0.7827 78.27%
CYP2C8 inhibition + 0.6481 64.81%
CYP inhibitory promiscuity - 0.6048 60.48%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Danger 0.5459 54.59%
Eye corrosion - 0.9714 97.14%
Eye irritation - 0.9718 97.18%
Skin irritation - 0.6654 66.54%
Skin corrosion - 0.9388 93.88%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3973 39.73%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7793 77.93%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) II 0.4806 48.06%
Estrogen receptor binding + 0.8005 80.05%
Androgen receptor binding + 0.6044 60.44%
Thyroid receptor binding + 0.6656 66.56%
Glucocorticoid receptor binding + 0.7254 72.54%
Aromatase binding + 0.8134 81.34%
PPAR gamma + 0.6497 64.97%
Honey bee toxicity - 0.7618 76.18%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5066 50.66%
Fish aquatic toxicity + 0.8884 88.84%

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 98.78% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.81% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.30% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.65% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.06% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.30% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.26% 92.94%
CHEMBL2581 P07339 Cathepsin D 87.58% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.57% 99.23%
CHEMBL1255126 O15151 Protein Mdm4 83.84% 90.20%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.44% 94.00%
CHEMBL4208 P20618 Proteasome component C5 83.11% 90.00%
CHEMBL2535 P11166 Glucose transporter 83.08% 98.75%
CHEMBL1937 Q92769 Histone deacetylase 2 82.72% 94.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.04% 96.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.81% 91.07%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.20% 85.30%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.16% 100.00%

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 139585687
LOTUS LTS0011747
wikiData Q77489413