Asperversin C

Details

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Internal ID 0ef2c36b-d7c9-4852-a098-134ff825db16
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name methyl (3S)-3-[(5aR,7R,8S,9S,9aR)-7-acetyloxy-3,5a,9-trimethyl-1-oxo-8-prop-1-en-2-yl-7,8,9a,10-tetrahydro-6H-pyrano[4,3-b]chromen-9-yl]-3-acetyloxypropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H34O9/c1-13(2)23-19(33-15(4)27)12-25(6)20(10-17-18(35-25)9-14(3)32-24(17)30)26(23,7)21(34-16(5)28)11-22(29)31-8/h9,19-21,23H,1,10-12H2,2-8H3/t19-,20+,21+,23-,25-,26+/m1/s1
InChI Key YXSFOIHUGDEKQU-LUNSLZPNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H34O9
Molecular Weight 490.50 g/mol
Exact Mass 490.22028266 g/mol
Topological Polar Surface Area (TPSA) 114.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.29
H-Bond Acceptor 9
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Asperversin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.5054 50.54%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6998 69.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8871 88.71%
OATP1B3 inhibitior + 0.8112 81.12%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8806 88.06%
P-glycoprotein inhibitior + 0.8133 81.33%
P-glycoprotein substrate + 0.5904 59.04%
CYP3A4 substrate + 0.6805 68.05%
CYP2C9 substrate + 0.6236 62.36%
CYP2D6 substrate - 0.8736 87.36%
CYP3A4 inhibition + 0.5308 53.08%
CYP2C9 inhibition - 0.8719 87.19%
CYP2C19 inhibition - 0.6309 63.09%
CYP2D6 inhibition - 0.9496 94.96%
CYP1A2 inhibition - 0.6161 61.61%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.6502 65.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.6807 68.07%
Eye corrosion - 0.9878 98.78%
Eye irritation - 0.8531 85.31%
Skin irritation - 0.7407 74.07%
Skin corrosion - 0.9549 95.49%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5090 50.90%
Micronuclear - 0.6100 61.00%
Hepatotoxicity - 0.5968 59.68%
skin sensitisation - 0.7519 75.19%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.6644 66.44%
Acute Oral Toxicity (c) III 0.4533 45.33%
Estrogen receptor binding + 0.7764 77.64%
Androgen receptor binding + 0.7089 70.89%
Thyroid receptor binding + 0.5407 54.07%
Glucocorticoid receptor binding + 0.7799 77.99%
Aromatase binding + 0.5605 56.05%
PPAR gamma + 0.7425 74.25%
Honey bee toxicity - 0.6521 65.21%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5300 53.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.44% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.23% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.99% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.26% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.60% 96.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 91.38% 94.80%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.49% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.47% 86.33%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 87.93% 95.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.47% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.43% 99.17%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 86.06% 89.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.68% 95.56%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.88% 97.21%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.81% 91.07%
CHEMBL3401 O75469 Pregnane X receptor 84.52% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 83.64% 91.19%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.83% 97.28%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.62% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.53% 94.00%

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 139590631
LOTUS LTS0248397
wikiData Q105368108