Aspereusin D

Details

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Internal ID 9a4cd7d5-eee8-49c8-a967-04cbd9a0adf0
Taxonomy Benzenoids > Benzene and substituted derivatives > Methoxybenzenes > Dimethoxybenzenes
IUPAC Name cis-(2S,3R)-2-[(2,4-dimethoxy-6-methylphenyl)methyl]-2-(hydroxymethyl)-3-methylcyclopentan-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H24O4/c1-11-7-13(20-3)8-15(21-4)14(11)9-17(10-18)12(2)5-6-16(17)19/h7-8,12,18H,5-6,9-10H2,1-4H3/t12-,17-/m1/s1
InChI Key QNUWWXUBTHSGPY-SJKOYZFVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H24O4
Molecular Weight 292.40 g/mol
Exact Mass 292.16745924 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Aspereusin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.8620 86.20%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.9130 91.30%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.9391 93.91%
OATP1B3 inhibitior + 0.8910 89.10%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.5627 56.27%
P-glycoprotein inhibitior - 0.8847 88.47%
P-glycoprotein substrate - 0.8537 85.37%
CYP3A4 substrate + 0.5346 53.46%
CYP2C9 substrate - 0.7948 79.48%
CYP2D6 substrate - 0.7247 72.47%
CYP3A4 inhibition - 0.5755 57.55%
CYP2C9 inhibition - 0.5425 54.25%
CYP2C19 inhibition - 0.6436 64.36%
CYP2D6 inhibition - 0.9462 94.62%
CYP1A2 inhibition + 0.6852 68.52%
CYP2C8 inhibition - 0.7206 72.06%
CYP inhibitory promiscuity - 0.8593 85.93%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7643 76.43%
Carcinogenicity (trinary) Non-required 0.6438 64.38%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.8811 88.11%
Skin irritation - 0.7613 76.13%
Skin corrosion - 0.9794 97.94%
Ames mutagenesis - 0.7254 72.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6759 67.59%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5040 50.40%
skin sensitisation - 0.8446 84.46%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.7685 76.85%
Acute Oral Toxicity (c) III 0.5725 57.25%
Estrogen receptor binding - 0.6215 62.15%
Androgen receptor binding - 0.4922 49.22%
Thyroid receptor binding + 0.5809 58.09%
Glucocorticoid receptor binding + 0.6532 65.32%
Aromatase binding - 0.5516 55.16%
PPAR gamma + 0.5982 59.82%
Honey bee toxicity - 0.9007 90.07%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9645 96.45%

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 94.50% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.11% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.02% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.36% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.77% 92.94%
CHEMBL4208 P20618 Proteasome component C5 89.68% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.32% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.66% 92.62%
CHEMBL4581 P52732 Kinesin-like protein 1 86.38% 93.18%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.88% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.86% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.72% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.49% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.18% 99.17%
CHEMBL2581 P07339 Cathepsin D 84.44% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.92% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.43% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.39% 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 139590894
LOTUS LTS0145451
wikiData Q105224669