Austalide R

Details

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Internal ID bac50f9b-15f2-4f9d-bd0d-f73f5aa8061f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthenes
IUPAC Name (1R,2R,4S,15S,16S,17R,20S)-2,15,20-trihydroxy-13-methoxy-4,7,17,22,22-pentamethyl-5,10,21,23-tetraoxahexacyclo[18.2.1.01,17.04,16.06,14.08,12]tricosa-6(14),7,12-trien-11-one
SMILES (Canonical) CC1=C2COC(=O)C2=C(C3=C1OC4(CC(C56C(OC(O5)(CCC6(C4C3O)C)O)(C)C)O)C)OC
SMILES (Isomeric) CC1=C2COC(=O)C2=C(C3=C1O[C@]4(C[C@H]([C@@]56[C@@]([C@H]4[C@@H]3O)(CC[C@@](O5)(OC6(C)C)O)C)O)C)OC
InChI InChI=1S/C25H32O9/c1-11-12-10-31-20(28)14(12)18(30-6)15-16(27)19-22(4)7-8-24(29)33-21(2,3)25(22,34-24)13(26)9-23(19,5)32-17(11)15/h13,16,19,26-27,29H,7-10H2,1-6H3/t13-,16-,19-,22-,23+,24+,25-/m1/s1
InChI Key PUKOIDBGERLELO-BPVTVUGRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H32O9
Molecular Weight 476.50 g/mol
Exact Mass 476.20463259 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 2.25
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Austalide R

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9797 97.97%
Caco-2 - 0.6240 62.40%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7499 74.99%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9091 90.91%
OATP1B3 inhibitior + 0.8303 83.03%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8672 86.72%
P-glycoprotein inhibitior - 0.4714 47.14%
P-glycoprotein substrate - 0.5797 57.97%
CYP3A4 substrate + 0.6869 68.69%
CYP2C9 substrate - 0.8002 80.02%
CYP2D6 substrate - 0.8226 82.26%
CYP3A4 inhibition - 0.8257 82.57%
CYP2C9 inhibition - 0.7334 73.34%
CYP2C19 inhibition - 0.7338 73.38%
CYP2D6 inhibition - 0.8728 87.28%
CYP1A2 inhibition - 0.5942 59.42%
CYP2C8 inhibition + 0.5602 56.02%
CYP inhibitory promiscuity - 0.8999 89.99%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5562 55.62%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.8193 81.93%
Skin irritation - 0.7892 78.92%
Skin corrosion - 0.9387 93.87%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6413 64.13%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.5680 56.80%
skin sensitisation - 0.8597 85.97%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.5092 50.92%
Acute Oral Toxicity (c) III 0.3976 39.76%
Estrogen receptor binding + 0.7721 77.21%
Androgen receptor binding + 0.7341 73.41%
Thyroid receptor binding + 0.6410 64.10%
Glucocorticoid receptor binding + 0.7929 79.29%
Aromatase binding + 0.8735 87.35%
PPAR gamma + 0.6556 65.56%
Honey bee toxicity - 0.7799 77.99%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9315 93.15%

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 95.70% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.07% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.14% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.29% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.26% 85.14%
CHEMBL4040 P28482 MAP kinase ERK2 88.92% 83.82%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.74% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.79% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.41% 97.14%
CHEMBL1871 P10275 Androgen Receptor 86.50% 96.43%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.79% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.11% 86.33%
CHEMBL2581 P07339 Cathepsin D 85.01% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.10% 96.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.08% 100.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 82.92% 82.38%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.84% 96.77%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.43% 92.62%
CHEMBL1937 Q92769 Histone deacetylase 2 82.18% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.88% 94.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.73% 97.25%

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 102339292
LOTUS LTS0215991
wikiData Q77280800