Aspergillicin D

Details

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Internal ID c08fabb2-f101-45a7-b902-607f55397649
Taxonomy Organic acids and derivatives > Peptidomimetics > Depsipeptides > Cyclic depsipeptides
IUPAC Name N-[(3S,9R,12S,13R,16S,19S,22S)-19-benzyl-9-[(2S)-butan-2-yl]-13-methyl-2,8,11,15,18,21-hexaoxo-16-propan-2-yl-14-oxa-1,7,10,17,20-pentazatricyclo[20.3.0.03,7]pentacosan-12-yl]acetamide
SMILES (Canonical) CCC(C)C1C(=O)N2CCCC2C(=O)N3CCCC3C(=O)NC(C(=O)NC(C(=O)OC(C(C(=O)N1)NC(=O)C)C)C(C)C)CC4=CC=CC=C4
SMILES (Isomeric) CC[C@H](C)[C@@H]1C(=O)N2CCC[C@H]2C(=O)N3CCC[C@H]3C(=O)N[C@H](C(=O)N[C@H](C(=O)O[C@@H]([C@@H](C(=O)N1)NC(=O)C)C)C(C)C)CC4=CC=CC=C4
InChI InChI=1S/C36H52N6O8/c1-7-21(4)29-35(48)42-18-12-16-27(42)34(47)41-17-11-15-26(41)32(45)38-25(19-24-13-9-8-10-14-24)31(44)39-28(20(2)3)36(49)50-22(5)30(33(46)40-29)37-23(6)43/h8-10,13-14,20-22,25-30H,7,11-12,15-19H2,1-6H3,(H,37,43)(H,38,45)(H,39,44)(H,40,46)/t21-,22+,25-,26-,27-,28-,29+,30-/m0/s1
InChI Key NRXZQMCJXXMPFH-QKUSIRIFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C36H52N6O8
Molecular Weight 696.80 g/mol
Exact Mass 696.38466264 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 0.82
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Aspergillicin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7315 73.15%
Caco-2 - 0.8498 84.98%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.4912 49.12%
OATP2B1 inhibitior + 0.5668 56.68%
OATP1B1 inhibitior + 0.8275 82.75%
OATP1B3 inhibitior + 0.9269 92.69%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9317 93.17%
P-glycoprotein inhibitior + 0.7875 78.75%
P-glycoprotein substrate + 0.8464 84.64%
CYP3A4 substrate + 0.6475 64.75%
CYP2C9 substrate - 0.6017 60.17%
CYP2D6 substrate - 0.8219 82.19%
CYP3A4 inhibition - 0.7457 74.57%
CYP2C9 inhibition - 0.8984 89.84%
CYP2C19 inhibition - 0.8307 83.07%
CYP2D6 inhibition - 0.8769 87.69%
CYP1A2 inhibition - 0.9219 92.19%
CYP2C8 inhibition - 0.5750 57.50%
CYP inhibitory promiscuity - 0.9296 92.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6344 63.44%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.9298 92.98%
Skin irritation - 0.7866 78.66%
Skin corrosion - 0.9317 93.17%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3807 38.07%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.7069 70.69%
skin sensitisation - 0.8873 88.73%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.6125 61.25%
Acute Oral Toxicity (c) III 0.6368 63.68%
Estrogen receptor binding + 0.7797 77.97%
Androgen receptor binding + 0.6562 65.62%
Thyroid receptor binding + 0.5503 55.03%
Glucocorticoid receptor binding + 0.6844 68.44%
Aromatase binding + 0.6100 61.00%
PPAR gamma + 0.7841 78.41%
Honey bee toxicity - 0.8299 82.99%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9466 94.66%

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 99.72% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.87% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.05% 96.09%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 95.24% 97.64%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 91.82% 93.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.81% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 89.57% 90.08%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.28% 95.89%
CHEMBL333 P08253 Matrix metalloproteinase-2 86.92% 96.31%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.04% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.73% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.55% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 84.88% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.74% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.81% 97.09%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 83.20% 95.83%
CHEMBL3524 P56524 Histone deacetylase 4 83.15% 92.97%
CHEMBL1902 P62942 FK506-binding protein 1A 81.82% 97.05%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.72% 82.38%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.63% 99.23%
CHEMBL4072 P07858 Cathepsin B 81.56% 93.67%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.54% 93.00%
CHEMBL3401 O75469 Pregnane X receptor 80.12% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.06% 89.00%

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 11028873
LOTUS LTS0218847
wikiData Q77503918