Aspergiside B

Details

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Internal ID ad44620f-9320-4a6d-b10f-c85ca9e16801
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 6-[(E)-but-2-en-2-yl]-4-(2,4-dihydroxy-6-methylbenzoyl)oxy-2-hydroxy-3-methylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20O7/c1-5-9(2)13-8-15(11(4)18(23)17(13)19(24)25)27-20(26)16-10(3)6-12(21)7-14(16)22/h5-8,21-23H,1-4H3,(H,24,25)/b9-5+
InChI Key MSAPYHMOHNMMPH-WEVVVXLNSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O7
Molecular Weight 372.40 g/mol
Exact Mass 372.12090297 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 3.76
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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CHEMBL4856066

2D Structure

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2D Structure of Aspergiside B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9775 97.75%
Caco-2 + 0.6217 62.17%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8361 83.61%
OATP2B1 inhibitior - 0.5634 56.34%
OATP1B1 inhibitior + 0.9204 92.04%
OATP1B3 inhibitior - 0.2438 24.38%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5975 59.75%
P-glycoprotein inhibitior - 0.7732 77.32%
P-glycoprotein substrate - 0.8402 84.02%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6089 60.89%
CYP2D6 substrate - 0.9067 90.67%
CYP3A4 inhibition - 0.7189 71.89%
CYP2C9 inhibition + 0.7429 74.29%
CYP2C19 inhibition + 0.7309 73.09%
CYP2D6 inhibition - 0.8414 84.14%
CYP1A2 inhibition + 0.7467 74.67%
CYP2C8 inhibition + 0.6972 69.72%
CYP inhibitory promiscuity + 0.7173 71.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7307 73.07%
Carcinogenicity (trinary) Non-required 0.5558 55.58%
Eye corrosion - 0.9941 99.41%
Eye irritation + 0.5821 58.21%
Skin irritation - 0.7876 78.76%
Skin corrosion - 0.9579 95.79%
Ames mutagenesis - 0.6115 61.15%
Human Ether-a-go-go-Related Gene inhibition - 0.3682 36.82%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.6788 67.88%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.6325 63.25%
Acute Oral Toxicity (c) III 0.4831 48.31%
Estrogen receptor binding + 0.8726 87.26%
Androgen receptor binding + 0.6841 68.41%
Thyroid receptor binding - 0.5947 59.47%
Glucocorticoid receptor binding + 0.6333 63.33%
Aromatase binding + 0.5443 54.43%
PPAR gamma + 0.6920 69.20%
Honey bee toxicity - 0.7935 79.35%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL3194 P02766 Transthyretin 94.37% 90.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 93.71% 94.42%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 93.32% 95.50%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.60% 97.21%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.35% 81.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.04% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.96% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 88.87% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.61% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.34% 96.95%
CHEMBL2581 P07339 Cathepsin D 86.95% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.44% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.55% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.10% 89.00%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 84.61% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.55% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.01% 96.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.27% 97.36%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.27% 99.15%
CHEMBL340 P08684 Cytochrome P450 3A4 80.11% 91.19%

Plants that contains it

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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

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PubChem 139590289
LOTUS LTS0205265
wikiData Q105171050