4-acetamido-2,3-dihydroxy-N-[1-(8-hydroxy-1-oxo-3,4-dihydroisochromen-3-yl)-3-methylbutyl]butanamide

Details

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Internal ID 3f1e5a8a-6529-4abc-87af-f5478e421cb0
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 4-acetamido-2,3-dihydroxy-N-[1-(8-hydroxy-1-oxo-3,4-dihydroisochromen-3-yl)-3-methylbutyl]butanamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H28N2O7/c1-10(2)7-13(22-19(27)18(26)15(25)9-21-11(3)23)16-8-12-5-4-6-14(24)17(12)20(28)29-16/h4-6,10,13,15-16,18,24-26H,7-9H2,1-3H3,(H,21,23)(H,22,27)
InChI Key JKCOKUNVPWIXQY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28N2O7
Molecular Weight 408.40 g/mol
Exact Mass 408.18965124 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP 1.20
Atomic LogP (AlogP) -0.14
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-acetamido-2,3-dihydroxy-N-[1-(8-hydroxy-1-oxo-3,4-dihydroisochromen-3-yl)-3-methylbutyl]butanamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6752 67.52%
Caco-2 - 0.7251 72.51%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.4355 43.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8848 88.48%
OATP1B3 inhibitior + 0.9303 93.03%
MATE1 inhibitior - 0.8846 88.46%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7059 70.59%
P-glycoprotein inhibitior - 0.6034 60.34%
P-glycoprotein substrate + 0.7708 77.08%
CYP3A4 substrate + 0.6178 61.78%
CYP2C9 substrate + 0.6062 60.62%
CYP2D6 substrate - 0.8461 84.61%
CYP3A4 inhibition - 0.9782 97.82%
CYP2C9 inhibition - 0.9076 90.76%
CYP2C19 inhibition - 0.8434 84.34%
CYP2D6 inhibition - 0.8373 83.73%
CYP1A2 inhibition - 0.8705 87.05%
CYP2C8 inhibition - 0.8636 86.36%
CYP inhibitory promiscuity - 0.9407 94.07%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6235 62.35%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9739 97.39%
Skin irritation - 0.7995 79.95%
Skin corrosion - 0.9455 94.55%
Ames mutagenesis - 0.5454 54.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5852 58.52%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.5443 54.43%
skin sensitisation - 0.8756 87.56%
Respiratory toxicity + 0.8444 84.44%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.5362 53.62%
Acute Oral Toxicity (c) III 0.6565 65.65%
Estrogen receptor binding + 0.7030 70.30%
Androgen receptor binding + 0.5712 57.12%
Thyroid receptor binding + 0.6349 63.49%
Glucocorticoid receptor binding + 0.5992 59.92%
Aromatase binding - 0.5891 58.91%
PPAR gamma + 0.5517 55.17%
Honey bee toxicity - 0.9055 90.55%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.7847 78.47%

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 99.43% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.54% 91.11%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 97.01% 83.10%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.85% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.97% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.59% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.14% 99.23%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.96% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 91.71% 94.73%
CHEMBL2094135 Q96BI3 Gamma-secretase 91.69% 98.05%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.59% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.87% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 89.17% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.31% 97.09%
CHEMBL5028 O14672 ADAM10 83.71% 97.50%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.52% 97.21%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.29% 97.14%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 83.15% 89.33%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.91% 100.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.67% 99.15%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 82.39% 80.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.07% 90.71%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 80.49% 96.67%
CHEMBL2535 P11166 Glucose transporter 80.16% 98.75%

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 163044656
LOTUS LTS0215362
wikiData Q105130141