Austalide M

Details

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Internal ID 783acc74-94d9-4611-ab5b-12560d9b1082
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthenes
IUPAC Name (1R,2R,4S,15S,16S,17R,20S)-2-hydroxy-13,15,20-trimethoxy-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/C27H36O9/c1-13-14-12-33-22(29)16(14)19(30-6)17-18(13)34-25(5)11-15(28)27-23(2,3)35-26(32-8,36-27)10-9-24(27,4)21(25)20(17)31-7/h15,20-21,28H,9-12H2,1-8H3/t15-,20-,21-,24-,25+,26+,27-/m1/s1
InChI Key OMVDEMLRFJDVFO-VGMMAMMESA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C27H36O9
Molecular Weight 504.60 g/mol
Exact Mass 504.23593272 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 3.56
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Austalide M

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9795 97.95%
Caco-2 - 0.5820 58.20%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7137 71.37%
OATP2B1 inhibitior - 0.8608 86.08%
OATP1B1 inhibitior + 0.8852 88.52%
OATP1B3 inhibitior + 0.8743 87.43%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9456 94.56%
P-glycoprotein inhibitior + 0.6448 64.48%
P-glycoprotein substrate + 0.5000 50.00%
CYP3A4 substrate + 0.6989 69.89%
CYP2C9 substrate - 0.8015 80.15%
CYP2D6 substrate - 0.8247 82.47%
CYP3A4 inhibition - 0.8126 81.26%
CYP2C9 inhibition - 0.7084 70.84%
CYP2C19 inhibition - 0.6630 66.30%
CYP2D6 inhibition - 0.8492 84.92%
CYP1A2 inhibition - 0.6490 64.90%
CYP2C8 inhibition + 0.6364 63.64%
CYP inhibitory promiscuity - 0.8984 89.84%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5559 55.59%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.8213 82.13%
Skin irritation - 0.7881 78.81%
Skin corrosion - 0.9402 94.02%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6260 62.60%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5802 58.02%
skin sensitisation - 0.8472 84.72%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6903 69.03%
Acute Oral Toxicity (c) III 0.3694 36.94%
Estrogen receptor binding + 0.8085 80.85%
Androgen receptor binding + 0.7590 75.90%
Thyroid receptor binding + 0.6772 67.72%
Glucocorticoid receptor binding + 0.8381 83.81%
Aromatase binding + 0.8468 84.68%
PPAR gamma + 0.7409 74.09%
Honey bee toxicity - 0.7800 78.00%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9167 91.67%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.52% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.34% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.16% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.35% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.07% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.05% 89.00%
CHEMBL2581 P07339 Cathepsin D 90.36% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.50% 94.45%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.98% 97.14%
CHEMBL1871 P10275 Androgen Receptor 87.85% 96.43%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 87.13% 82.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.93% 97.09%
CHEMBL2535 P11166 Glucose transporter 85.75% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.26% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.93% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.81% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.03% 94.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.72% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.48% 85.14%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.89% 93.40%
CHEMBL4208 P20618 Proteasome component C5 80.83% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.53% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.47% 97.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.28% 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 56839628
LOTUS LTS0088842
wikiData Q105194524