Asperterrestide A

Details

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Internal ID 89ac16ed-696f-4132-9a3b-826ea92f945b
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name (4R,7R,10R)-7-butan-2-yl-4-[(S)-hydroxy(phenyl)methyl]-5,10-dimethyl-2,5,8,11-tetrazabicyclo[11.4.0]heptadeca-1(17),13,15-triene-3,6,9,12-tetrone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H32N4O5/c1-5-15(2)20-26(35)30(4)21(22(31)17-11-7-6-8-12-17)25(34)28-19-14-10-9-13-18(19)24(33)27-16(3)23(32)29-20/h6-16,20-22,31H,5H2,1-4H3,(H,27,33)(H,28,34)(H,29,32)/t15?,16-,20-,21-,22+/m1/s1
InChI Key AQBNNSWAQPPMPF-QZPRSPPASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H32N4O5
Molecular Weight 480.60 g/mol
Exact Mass 480.23727013 g/mol
Topological Polar Surface Area (TPSA) 128.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.85
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Asperterrestide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7183 71.83%
Caco-2 - 0.6658 66.58%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5414 54.14%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.8348 83.48%
OATP1B3 inhibitior + 0.9219 92.19%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9568 95.68%
BSEP inhibitior + 0.8286 82.86%
P-glycoprotein inhibitior + 0.7172 71.72%
P-glycoprotein substrate + 0.7163 71.63%
CYP3A4 substrate + 0.5944 59.44%
CYP2C9 substrate + 0.6043 60.43%
CYP2D6 substrate - 0.8578 85.78%
CYP3A4 inhibition - 0.6920 69.20%
CYP2C9 inhibition - 0.8264 82.64%
CYP2C19 inhibition - 0.8233 82.33%
CYP2D6 inhibition - 0.8869 88.69%
CYP1A2 inhibition - 0.6628 66.28%
CYP2C8 inhibition - 0.7752 77.52%
CYP inhibitory promiscuity - 0.9113 91.13%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7710 77.10%
Carcinogenicity (trinary) Non-required 0.6545 65.45%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9779 97.79%
Skin irritation - 0.8179 81.79%
Skin corrosion - 0.9525 95.25%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7240 72.40%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.9108 91.08%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6129 61.29%
Acute Oral Toxicity (c) III 0.6853 68.53%
Estrogen receptor binding + 0.5286 52.86%
Androgen receptor binding + 0.6759 67.59%
Thyroid receptor binding + 0.5654 56.54%
Glucocorticoid receptor binding + 0.6880 68.80%
Aromatase binding - 0.6569 65.69%
PPAR gamma + 0.6737 67.37%
Honey bee toxicity - 0.8319 83.19%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8781 87.81%

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 99.69% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.58% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.38% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.03% 85.14%
CHEMBL221 P23219 Cyclooxygenase-1 95.00% 90.17%
CHEMBL4208 P20618 Proteasome component C5 91.16% 90.00%
CHEMBL202 P00374 Dihydrofolate reductase 90.22% 89.92%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.12% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.02% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 88.90% 94.75%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.55% 93.03%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.68% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.34% 91.11%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.74% 90.24%
CHEMBL226 P30542 Adenosine A1 receptor 82.70% 95.93%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.03% 100.00%
CHEMBL2443 P49862 Kallikrein 7 80.60% 94.00%

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 71726177
LOTUS LTS0030674
wikiData Q75062922