Austocystinc

Details

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Internal ID 573fd19a-cc3b-44c3-90f6-693c5b53918b
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 18-hydroxy-15-(3-hydroxy-3-methylbutyl)-2-methoxy-7,9,13-trioxapentacyclo[10.8.0.03,10.04,8.014,19]icosa-1,3(10),5,11,14,16,18-heptaen-20-one
SMILES (Canonical) CC(C)(CCC1=C2C(=C(C=C1)O)C(=O)C3=C(C4=C(C=C3O2)OC5C4C=CO5)OC)O
SMILES (Isomeric) CC(C)(CCC1=C2C(=C(C=C1)O)C(=O)C3=C(C4=C(C=C3O2)OC5C4C=CO5)OC)O
InChI InChI=1S/C23H22O7/c1-23(2,26)8-6-11-4-5-13(24)17-19(25)18-15(29-20(11)17)10-14-16(21(18)27-3)12-7-9-28-22(12)30-14/h4-5,7,9-10,12,22,24,26H,6,8H2,1-3H3
InChI Key MLCZRFXGJOUFHE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H22O7
Molecular Weight 410.40 g/mol
Exact Mass 410.13655304 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.71
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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55256-55-8
AKOS040734750
NCGC00386095-01!

2D Structure

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2D Structure of Austocystinc

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 - 0.6331 63.31%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7891 78.91%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8947 89.47%
OATP1B3 inhibitior + 0.8098 80.98%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.7678 76.78%
P-glycoprotein inhibitior + 0.6934 69.34%
P-glycoprotein substrate - 0.5797 57.97%
CYP3A4 substrate + 0.6358 63.58%
CYP2C9 substrate - 0.5923 59.23%
CYP2D6 substrate - 0.8402 84.02%
CYP3A4 inhibition - 0.7554 75.54%
CYP2C9 inhibition - 0.8016 80.16%
CYP2C19 inhibition - 0.8255 82.55%
CYP2D6 inhibition - 0.7937 79.37%
CYP1A2 inhibition - 0.7715 77.15%
CYP2C8 inhibition + 0.7388 73.88%
CYP inhibitory promiscuity - 0.7399 73.99%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.4403 44.03%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.8478 84.78%
Skin irritation - 0.7707 77.07%
Skin corrosion - 0.9282 92.82%
Ames mutagenesis + 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4822 48.22%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8065 80.65%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8894 88.94%
Acute Oral Toxicity (c) I 0.3952 39.52%
Estrogen receptor binding + 0.8643 86.43%
Androgen receptor binding + 0.7732 77.32%
Thyroid receptor binding + 0.5607 56.07%
Glucocorticoid receptor binding + 0.9031 90.31%
Aromatase binding + 0.7093 70.93%
PPAR gamma + 0.8699 86.99%
Honey bee toxicity - 0.7849 78.49%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9691 96.91%

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 99.57% 91.11%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 93.65% 80.78%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.12% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.33% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.14% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.53% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.40% 94.45%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 90.17% 92.68%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.71% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 89.65% 94.73%
CHEMBL2581 P07339 Cathepsin D 87.44% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.18% 99.15%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.30% 92.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.97% 99.23%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.34% 86.92%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.67% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.43% 99.17%
CHEMBL2535 P11166 Glucose transporter 81.51% 98.75%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.17% 95.71%

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 73715386
LOTUS LTS0231933
wikiData Q105166513