Exumolide A

Details

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Internal ID 53c41180-fe26-42e0-b636-732948b29e87
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name (3S,6S,12S,15S,18S,21S)-12,15-dibenzyl-19-methyl-3,18-bis(2-methylpropyl)-4-oxa-1,10,13,16,19-pentazatricyclo[19.3.0.06,10]tetracosane-2,5,11,14,17,20-hexone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C41H55N5O7/c1-26(2)22-34-37(48)42-30(24-28-14-8-6-9-15-28)36(47)43-31(25-29-16-10-7-11-17-29)38(49)46-21-13-19-33(46)41(52)53-35(23-27(3)4)40(51)45-20-12-18-32(45)39(50)44(34)5/h6-11,14-17,26-27,30-35H,12-13,18-25H2,1-5H3,(H,42,48)(H,43,47)/t30-,31-,32-,33-,34-,35-/m0/s1
InChI Key GWGKNTICBPKKKW-LBBUGJAGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C41H55N5O7
Molecular Weight 729.90 g/mol
Exact Mass 729.41014911 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP 5.70
Atomic LogP (AlogP) 3.27
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Exumolide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5000 50.00%
Caco-2 - 0.8060 80.60%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Lysosomes 0.5251 52.51%
OATP2B1 inhibitior - 0.5642 56.42%
OATP1B1 inhibitior + 0.8756 87.56%
OATP1B3 inhibitior + 0.9198 91.98%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9173 91.73%
P-glycoprotein inhibitior + 0.8208 82.08%
P-glycoprotein substrate + 0.7964 79.64%
CYP3A4 substrate + 0.6476 64.76%
CYP2C9 substrate - 0.6147 61.47%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.6800 68.00%
CYP2C9 inhibition - 0.7244 72.44%
CYP2C19 inhibition - 0.6835 68.35%
CYP2D6 inhibition - 0.9049 90.49%
CYP1A2 inhibition - 0.9616 96.16%
CYP2C8 inhibition - 0.6913 69.13%
CYP inhibitory promiscuity - 0.9521 95.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6165 61.65%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9314 93.14%
Skin irritation - 0.7915 79.15%
Skin corrosion - 0.9307 93.07%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7427 74.27%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.5929 59.29%
skin sensitisation - 0.9078 90.78%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6211 62.11%
Acute Oral Toxicity (c) III 0.6907 69.07%
Estrogen receptor binding + 0.7950 79.50%
Androgen receptor binding + 0.7343 73.43%
Thyroid receptor binding + 0.5748 57.48%
Glucocorticoid receptor binding + 0.7433 74.33%
Aromatase binding + 0.5485 54.85%
PPAR gamma + 0.7784 77.84%
Honey bee toxicity - 0.8727 87.27%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9550 95.50%

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
CHEMBL2581 P07339 Cathepsin D 99.71% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.62% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.38% 96.09%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 95.08% 97.64%
CHEMBL333 P08253 Matrix metalloproteinase-2 94.68% 96.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.65% 85.14%
CHEMBL5103 Q969S8 Histone deacetylase 10 94.46% 90.08%
CHEMBL1902 P62942 FK506-binding protein 1A 92.58% 97.05%
CHEMBL3524 P56524 Histone deacetylase 4 89.77% 92.97%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.96% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.91% 95.89%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 86.52% 82.38%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 86.44% 90.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.82% 94.45%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.22% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.22% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.07% 97.14%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.39% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.12% 86.33%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.08% 98.33%

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 10509145
LOTUS LTS0231117
wikiData Q77375638