(-)-aspersclerolide D

Details

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Internal ID b4ff9924-8f9d-4518-b4ca-218584e67cbc
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans
IUPAC Name (2R,3S)-7-hydroxy-4'-methoxy-3,5-dimethylspiro[3,4-dihydrochromene-2,5'-furan]-2'-one
SMILES (Canonical) CC1CC2=C(C=C(C=C2C)O)OC13C(=CC(=O)O3)OC
SMILES (Isomeric) C[C@H]1CC2=C(C=C(C=C2C)O)O[C@]13C(=CC(=O)O3)OC
InChI InChI=1S/C15H16O5/c1-8-4-10(16)6-12-11(8)5-9(2)15(19-12)13(18-3)7-14(17)20-15/h4,6-7,9,16H,5H2,1-3H3/t9-,15+/m0/s1
InChI Key XWMWNVWBHJDLED-BJOHPYRUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H16O5
Molecular Weight 276.28 g/mol
Exact Mass 276.09977361 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.06
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (-)-aspersclerolide D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9868 98.68%
Caco-2 + 0.8559 85.59%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6214 62.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9149 91.49%
OATP1B3 inhibitior + 0.8434 84.34%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6718 67.18%
P-glycoprotein inhibitior - 0.9019 90.19%
P-glycoprotein substrate - 0.7690 76.90%
CYP3A4 substrate + 0.5805 58.05%
CYP2C9 substrate - 0.6044 60.44%
CYP2D6 substrate - 0.8578 85.78%
CYP3A4 inhibition - 0.5298 52.98%
CYP2C9 inhibition - 0.8817 88.17%
CYP2C19 inhibition + 0.5643 56.43%
CYP2D6 inhibition - 0.6757 67.57%
CYP1A2 inhibition - 0.5331 53.31%
CYP2C8 inhibition - 0.7039 70.39%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Danger 0.5418 54.18%
Eye corrosion - 0.9792 97.92%
Eye irritation - 0.8551 85.51%
Skin irritation - 0.6879 68.79%
Skin corrosion - 0.9620 96.20%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4059 40.59%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.5296 52.96%
skin sensitisation - 0.7367 73.67%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.5985 59.85%
Acute Oral Toxicity (c) II 0.5564 55.64%
Estrogen receptor binding + 0.6496 64.96%
Androgen receptor binding + 0.7540 75.40%
Thyroid receptor binding + 0.5255 52.55%
Glucocorticoid receptor binding + 0.5781 57.81%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7890 78.90%
Honey bee toxicity - 0.8245 82.45%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9773 97.73%

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 99.15% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.38% 85.14%
CHEMBL2581 P07339 Cathepsin D 93.25% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.67% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.87% 96.09%
CHEMBL4208 P20618 Proteasome component C5 88.99% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.35% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.56% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.26% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.20% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.14% 92.94%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 85.61% 82.38%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.44% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.16% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.11% 94.80%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 84.01% 93.40%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.73% 86.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.41% 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 146682631
LOTUS LTS0262140
wikiData Q105343617