Austalide O

Details

Top
Internal ID 9f1f6fc8-6cfb-40ab-a12b-4f8499da77d9
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthenes
IUPAC Name (1R,2R,4S,15S,16S,17R,20S)-2,15-dihydroxy-13,20-dimethoxy-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)
SMILES (Isomeric)
InChI InChI=1S/C26H34O9/c1-12-13-11-32-21(29)15(13)19(30-6)16-17(28)20-23(4)8-9-25(31-7)34-22(2,3)26(23,35-25)14(27)10-24(20,5)33-18(12)16/h14,17,20,27-28H,8-11H2,1-7H3/t14-,17-,20-,23-,24+,25+,26-/m1/s1
InChI Key RWUXVAPZLXXYCR-KVFIAQGVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C26H34O9
Molecular Weight 490.50 g/mol
Exact Mass 490.22028266 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.90
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Austalide O

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9725 97.25%
Caco-2 - 0.6110 61.10%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7379 73.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8924 89.24%
OATP1B3 inhibitior + 0.8997 89.97%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9368 93.68%
P-glycoprotein inhibitior + 0.5785 57.85%
P-glycoprotein substrate - 0.5485 54.85%
CYP3A4 substrate + 0.6927 69.27%
CYP2C9 substrate - 0.8002 80.02%
CYP2D6 substrate - 0.8214 82.14%
CYP3A4 inhibition - 0.8447 84.47%
CYP2C9 inhibition - 0.7569 75.69%
CYP2C19 inhibition - 0.7281 72.81%
CYP2D6 inhibition - 0.8497 84.97%
CYP1A2 inhibition - 0.6366 63.66%
CYP2C8 inhibition + 0.6223 62.23%
CYP inhibitory promiscuity - 0.8781 87.81%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5487 54.87%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8199 81.99%
Skin irritation - 0.7864 78.64%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6136 61.36%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation - 0.8521 85.21%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6166 61.66%
Acute Oral Toxicity (c) III 0.3998 39.98%
Estrogen receptor binding + 0.8086 80.86%
Androgen receptor binding + 0.7436 74.36%
Thyroid receptor binding + 0.6740 67.40%
Glucocorticoid receptor binding + 0.8231 82.31%
Aromatase binding + 0.8545 85.45%
PPAR gamma + 0.6758 67.58%
Honey bee toxicity - 0.7879 78.79%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9214 92.14%

Targets

Top

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
CHEMBL4040 P28482 MAP kinase ERK2 99.11% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.17% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.98% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.97% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.94% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.52% 99.23%
CHEMBL2581 P07339 Cathepsin D 89.02% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.66% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.34% 97.14%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.89% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.71% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.38% 97.09%
CHEMBL1871 P10275 Androgen Receptor 87.20% 96.43%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 86.81% 96.77%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 85.87% 82.38%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.69% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.93% 92.62%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.80% 93.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.27% 100.00%
CHEMBL2535 P11166 Glucose transporter 81.21% 98.75%
CHEMBL4208 P20618 Proteasome component C5 80.28% 90.00%

Plants that contains it

Top
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

Top
PubChem 56839852
LOTUS LTS0000737
wikiData Q77383472