Campyrone B

Details

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Internal ID c6b1030f-e188-4d48-b0df-72f47bd7b358
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name N-[(1S)-1-(4-methoxy-6-oxopyran-2-yl)-3-methylbutyl]acetamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H19NO4/c1-8(2)5-11(14-9(3)15)12-6-10(17-4)7-13(16)18-12/h6-8,11H,5H2,1-4H3,(H,14,15)/t11-/m0/s1
InChI Key PFIUOLPDUMSADF-NSHDSACASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H19NO4
Molecular Weight 253.29 g/mol
Exact Mass 253.13140809 g/mol
Topological Polar Surface Area (TPSA) 64.60 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.87
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Campyrone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9601 96.01%
Caco-2 + 0.7205 72.05%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5210 52.10%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.8995 89.95%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.8033 80.33%
OCT2 inhibitior - 0.8567 85.67%
BSEP inhibitior - 0.6941 69.41%
P-glycoprotein inhibitior - 0.9172 91.72%
P-glycoprotein substrate - 0.6000 60.00%
CYP3A4 substrate - 0.5498 54.98%
CYP2C9 substrate + 0.6027 60.27%
CYP2D6 substrate - 0.8686 86.86%
CYP3A4 inhibition - 0.9304 93.04%
CYP2C9 inhibition - 0.6411 64.11%
CYP2C19 inhibition - 0.8163 81.63%
CYP2D6 inhibition - 0.9005 90.05%
CYP1A2 inhibition - 0.7598 75.98%
CYP2C8 inhibition - 0.9532 95.32%
CYP inhibitory promiscuity - 0.7765 77.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8013 80.13%
Carcinogenicity (trinary) Non-required 0.6354 63.54%
Eye corrosion - 0.9884 98.84%
Eye irritation - 0.9085 90.85%
Skin irritation - 0.8379 83.79%
Skin corrosion - 0.9597 95.97%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7558 75.58%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.6158 61.58%
skin sensitisation - 0.9285 92.85%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5872 58.72%
Acute Oral Toxicity (c) III 0.6351 63.51%
Estrogen receptor binding - 0.6107 61.07%
Androgen receptor binding - 0.4910 49.10%
Thyroid receptor binding - 0.5644 56.44%
Glucocorticoid receptor binding - 0.6045 60.45%
Aromatase binding - 0.6040 60.40%
PPAR gamma + 0.7330 73.30%
Honey bee toxicity - 0.9424 94.24%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.5063 50.63%

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 97.89% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.44% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.56% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.30% 99.17%
CHEMBL4208 P20618 Proteasome component C5 90.27% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.81% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.80% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 88.55% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.78% 96.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.64% 91.07%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.42% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.36% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.08% 95.50%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 82.14% 80.00%
CHEMBL340 P08684 Cytochrome P450 3A4 81.98% 91.19%
CHEMBL3437 Q16853 Amine oxidase, copper containing 81.92% 94.00%
CHEMBL2535 P11166 Glucose transporter 81.36% 98.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.03% 97.14%

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 72197063
LOTUS LTS0154689
wikiData Q77567342