Asperlide A

Details

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Internal ID c5016530-545c-482d-b224-f09c74377049
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name methyl (2R)-4-hydroxy-2-[(3-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)methyl]-5-oxo-3-phenylfuran-2-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H24O7/c1-23(2)18(25)12-16-11-14(9-10-17(16)30-23)13-24(22(28)29-3)19(20(26)21(27)31-24)15-7-5-4-6-8-15/h4-11,18,25-26H,12-13H2,1-3H3/t18?,24-/m1/s1
InChI Key PSCBKXCZUOOZDC-VCUSLETLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H24O7
Molecular Weight 424.40 g/mol
Exact Mass 424.15220310 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.74
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEMBL4291550

2D Structure

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2D Structure of Asperlide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9796 97.96%
Caco-2 - 0.5503 55.03%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7479 74.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8493 84.93%
OATP1B3 inhibitior - 0.2166 21.66%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9817 98.17%
P-glycoprotein inhibitior + 0.5879 58.79%
P-glycoprotein substrate - 0.5907 59.07%
CYP3A4 substrate + 0.6403 64.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8268 82.68%
CYP3A4 inhibition - 0.5406 54.06%
CYP2C9 inhibition - 0.5398 53.98%
CYP2C19 inhibition - 0.6175 61.75%
CYP2D6 inhibition - 0.8479 84.79%
CYP1A2 inhibition - 0.7964 79.64%
CYP2C8 inhibition + 0.6969 69.69%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.4749 47.49%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.8914 89.14%
Skin irritation - 0.7409 74.09%
Skin corrosion - 0.9387 93.87%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6919 69.19%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.6983 69.83%
skin sensitisation - 0.8032 80.32%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.6628 66.28%
Acute Oral Toxicity (c) I 0.6409 64.09%
Estrogen receptor binding + 0.7848 78.48%
Androgen receptor binding + 0.7959 79.59%
Thyroid receptor binding + 0.5283 52.83%
Glucocorticoid receptor binding + 0.8085 80.85%
Aromatase binding + 0.5680 56.80%
PPAR gamma + 0.8021 80.21%
Honey bee toxicity - 0.7885 78.85%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9930 99.30%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.49% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.97% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.70% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.06% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 97.61% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.38% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 92.94% 90.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 92.91% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.51% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.86% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.34% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.23% 96.95%
CHEMBL5028 O14672 ADAM10 86.14% 97.50%
CHEMBL340 P08684 Cytochrome P450 3A4 82.79% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.23% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.85% 97.14%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.53% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.14% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 145988278
LOTUS LTS0187151
wikiData Q105214096