Emericellolide A

Details

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Internal ID 9e62dd3d-4ff5-4938-a451-0c038b052c15
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name methyl (4S,9R)-24-hydroxy-9-(2-hydroxypropan-2-yl)-21-methoxy-12,16-dimethyl-7,25-dioxo-8,19-dioxa-3-azatricyclo[18.3.1.13,23]pentacosa-1(24),12,16,20,22-pentaene-4-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H41NO9/c1-18-8-7-9-19(2)14-15-39-27-23(37-5)16-20-21(26(27)33)17-31(28(20)34)22(29(35)38-6)11-13-25(32)40-24(12-10-18)30(3,4)36/h8,14,16,22,24,33,36H,7,9-13,15,17H2,1-6H3/t22-,24+/m0/s1
InChI Key ZEKGYLQKGKLSCC-LADGPHEKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H41NO9
Molecular Weight 559.60 g/mol
Exact Mass 559.27813189 g/mol
Topological Polar Surface Area (TPSA) 132.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 4.21
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Emericellolide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9281 92.81%
Caco-2 - 0.7216 72.16%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6836 68.36%
OATP2B1 inhibitior - 0.7147 71.47%
OATP1B1 inhibitior + 0.8651 86.51%
OATP1B3 inhibitior + 0.9244 92.44%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9936 99.36%
P-glycoprotein inhibitior + 0.7975 79.75%
P-glycoprotein substrate + 0.6365 63.65%
CYP3A4 substrate + 0.6927 69.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8583 85.83%
CYP3A4 inhibition - 0.8168 81.68%
CYP2C9 inhibition - 0.8770 87.70%
CYP2C19 inhibition - 0.8500 85.00%
CYP2D6 inhibition - 0.9065 90.65%
CYP1A2 inhibition - 0.8957 89.57%
CYP2C8 inhibition + 0.7257 72.57%
CYP inhibitory promiscuity - 0.8843 88.43%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Danger 0.4931 49.31%
Eye corrosion - 0.9869 98.69%
Eye irritation - 0.9365 93.65%
Skin irritation - 0.7743 77.43%
Skin corrosion - 0.9290 92.90%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4919 49.19%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.5446 54.46%
skin sensitisation - 0.8478 84.78%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.5583 55.83%
Acute Oral Toxicity (c) III 0.6801 68.01%
Estrogen receptor binding + 0.7533 75.33%
Androgen receptor binding + 0.5831 58.31%
Thyroid receptor binding + 0.5246 52.46%
Glucocorticoid receptor binding + 0.8236 82.36%
Aromatase binding + 0.6910 69.10%
PPAR gamma + 0.6340 63.40%
Honey bee toxicity - 0.7914 79.14%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9499 94.99%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.11% 91.11%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 97.25% 98.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.17% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.92% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.62% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.21% 97.25%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.07% 96.77%
CHEMBL2535 P11166 Glucose transporter 91.09% 98.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.90% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.85% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.31% 86.33%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 89.28% 90.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.94% 99.17%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.74% 97.21%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.55% 96.09%
CHEMBL5747 Q92793 CREB-binding protein 87.33% 95.12%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.86% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.65% 91.19%
CHEMBL2056 P21728 Dopamine D1 receptor 82.58% 91.00%
CHEMBL1871 P10275 Androgen Receptor 82.15% 96.43%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.69% 97.14%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 80.82% 97.47%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.81% 95.89%
CHEMBL204 P00734 Thrombin 80.69% 96.01%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 80.50% 98.00%

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 139586835
LOTUS LTS0203310
wikiData Q77515538