Asterinin E

Details

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Internal ID 9c526a76-2693-44ff-93c9-64a1c76d48be
Taxonomy Organic acids and derivatives > Peptidomimetics > Hybrid peptides
IUPAC Name methyl 3-hydroxy-2-[[3-[[3-hydroxy-2-[[3-hydroxy-2-(1H-pyrrole-2-carbonylamino)butanoyl]amino]propanoyl]amino]-3-phenylpropanoyl]amino]butanoate
SMILES (Canonical) CC(C(C(=O)NC(CO)C(=O)NC(CC(=O)NC(C(C)O)C(=O)OC)C1=CC=CC=C1)NC(=O)C2=CC=CN2)O
SMILES (Isomeric) CC(C(C(=O)NC(CO)C(=O)NC(CC(=O)NC(C(C)O)C(=O)OC)C1=CC=CC=C1)NC(=O)C2=CC=CN2)O
InChI InChI=1S/C26H35N5O9/c1-14(33)21(31-23(36)17-10-7-11-27-17)25(38)29-19(13-32)24(37)28-18(16-8-5-4-6-9-16)12-20(35)30-22(15(2)34)26(39)40-3/h4-11,14-15,18-19,21-22,27,32-34H,12-13H2,1-3H3,(H,28,37)(H,29,38)(H,30,35)(H,31,36)
InChI Key CJCYMDBASVMOKO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H35N5O9
Molecular Weight 561.60 g/mol
Exact Mass 561.24347771 g/mol
Topological Polar Surface Area (TPSA) 219.00 Ų
XlogP -1.40
Atomic LogP (AlogP) -1.74
H-Bond Acceptor 9
H-Bond Donor 8
Rotatable Bonds 14

Synonyms

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172548-92-4
methyl 3-hydroxy-2-[[3-[[3-hydroxy-2-[[3-hydroxy-2-(1H-pyrrole-2-carbonylamino)butanoyl]amino]propanoyl]amino]-3-phenylpropanoyl]amino]butanoate
delta(2,4)-Pro-allo-thr-ser-betaphe-allo-throme
delta(2,4)-Pro-L-allo-thr-L-ser-L-betahe-L-allo-throme
2,3,4,5-Tetradehydroprolyl-allothreonyl-seryl-3-phenyl-beta-alanyl-L-allothreonine methyl ester
L-Allothreonine, N-(N-(N-(N-(2,3,4,5-tetradehydroprolyl)-L-allothreonyl)-L-seryl)-(R)-3-phenyl-beta-alanyl)-, methyl ester
C26H35N5O9
C26-H35-N5-O9
DTXSID40938171
AKOS040750608
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Asterinin E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8039 80.39%
Caco-2 - 0.8806 88.06%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7053 70.53%
OATP2B1 inhibitior + 0.5788 57.88%
OATP1B1 inhibitior + 0.8929 89.29%
OATP1B3 inhibitior + 0.9320 93.20%
MATE1 inhibitior - 0.8441 84.41%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9789 97.89%
P-glycoprotein inhibitior + 0.6467 64.67%
P-glycoprotein substrate + 0.6470 64.70%
CYP3A4 substrate + 0.6146 61.46%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate - 0.8370 83.70%
CYP3A4 inhibition - 0.7473 74.73%
CYP2C9 inhibition - 0.8692 86.92%
CYP2C19 inhibition - 0.8687 86.87%
CYP2D6 inhibition - 0.9282 92.82%
CYP1A2 inhibition - 0.7948 79.48%
CYP2C8 inhibition - 0.6519 65.19%
CYP inhibitory promiscuity - 0.8277 82.77%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6906 69.06%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.9536 95.36%
Skin irritation - 0.8316 83.16%
Skin corrosion - 0.9630 96.30%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7147 71.47%
Micronuclear + 0.7700 77.00%
Hepatotoxicity - 0.7166 71.66%
skin sensitisation - 0.9075 90.75%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6049 60.49%
Acute Oral Toxicity (c) III 0.6421 64.21%
Estrogen receptor binding + 0.6690 66.90%
Androgen receptor binding - 0.4858 48.58%
Thyroid receptor binding + 0.5468 54.68%
Glucocorticoid receptor binding + 0.5849 58.49%
Aromatase binding - 0.5877 58.77%
PPAR gamma + 0.7232 72.32%
Honey bee toxicity - 0.8624 86.24%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.8833 88.33%

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 99.21% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 97.90% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.11% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 94.44% 90.20%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.13% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.34% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 90.35% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.61% 95.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 89.41% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.23% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.71% 91.11%
CHEMBL3776 Q14790 Caspase-8 86.12% 97.06%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.68% 94.62%
CHEMBL202 P00374 Dihydrofolate reductase 84.67% 89.92%
CHEMBL2535 P11166 Glucose transporter 83.66% 98.75%
CHEMBL2095164 P49354 Geranylgeranyl transferase type I 83.24% 92.80%
CHEMBL5028 O14672 ADAM10 82.97% 97.50%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 81.50% 89.33%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.12% 94.08%

Plants that contains it

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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.
Aster tataricus

Cross-Links

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PubChem 3083496
NPASS NPC162422
LOTUS LTS0178756
wikiData Q82914425