Asperversin A

Details

Top
Internal ID 2b5f0f0f-ff53-4c5b-9fcd-6df6b2b9b0aa
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name methyl 2-[(1R,10R,11R,12S,15S,16R)-16-acetyloxy-1,5,11,14,14-pentamethyl-7-oxo-2,6,13-trioxatetracyclo[8.7.0.03,8.011,15]heptadeca-3(8),4-dien-12-yl]acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H32O8/c1-12-8-15-14(21(27)29-12)9-17-23(5,31-15)11-16(30-13(2)25)20-22(3,4)32-18(24(17,20)6)10-19(26)28-7/h8,16-18,20H,9-11H2,1-7H3/t16-,17+,18+,20+,23-,24+/m1/s1
InChI Key XZUBQSJKQPRBGE-GRAVRPJHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H32O8
Molecular Weight 448.50 g/mol
Exact Mass 448.20971797 g/mol
Topological Polar Surface Area (TPSA) 97.40 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.96
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Asperversin A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.5376 53.76%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7635 76.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8710 87.10%
OATP1B3 inhibitior + 0.9361 93.61%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9244 92.44%
P-glycoprotein inhibitior + 0.7683 76.83%
P-glycoprotein substrate + 0.5865 58.65%
CYP3A4 substrate + 0.6949 69.49%
CYP2C9 substrate - 0.5646 56.46%
CYP2D6 substrate - 0.8676 86.76%
CYP3A4 inhibition - 0.6419 64.19%
CYP2C9 inhibition - 0.7072 70.72%
CYP2C19 inhibition - 0.6888 68.88%
CYP2D6 inhibition - 0.9091 90.91%
CYP1A2 inhibition - 0.7447 74.47%
CYP2C8 inhibition + 0.6172 61.72%
CYP inhibitory promiscuity - 0.7605 76.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5889 58.89%
Eye corrosion - 0.9869 98.69%
Eye irritation - 0.8658 86.58%
Skin irritation - 0.8143 81.43%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis - 0.7164 71.64%
Human Ether-a-go-go-Related Gene inhibition + 0.6830 68.30%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.5912 59.12%
skin sensitisation - 0.8397 83.97%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.4940 49.40%
Acute Oral Toxicity (c) III 0.4234 42.34%
Estrogen receptor binding + 0.8553 85.53%
Androgen receptor binding + 0.7160 71.60%
Thyroid receptor binding + 0.5971 59.71%
Glucocorticoid receptor binding + 0.8379 83.79%
Aromatase binding + 0.6947 69.47%
PPAR gamma + 0.7547 75.47%
Honey bee toxicity - 0.7506 75.06%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9951 99.51%

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 98.99% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.35% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.29% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.71% 96.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.62% 94.80%
CHEMBL3922 P50579 Methionine aminopeptidase 2 88.93% 97.28%
CHEMBL2581 P07339 Cathepsin D 88.85% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.93% 95.56%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 84.52% 89.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.00% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.83% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.34% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.15% 100.00%
CHEMBL5028 O14672 ADAM10 82.94% 97.50%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.92% 95.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.89% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.98% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.60% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 80.44% 91.19%

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 139590626
LOTUS LTS0157978
wikiData Q105345176