Mycemycin B

Details

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Internal ID 18c648dd-9418-4b1b-a935-5e0d31d63adf
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Diarylethers
IUPAC Name methyl 8-chloro-6-oxo-5H-benzo[b][1,4]benzoxazepine-4-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H10ClNO4/c1-20-15(19)9-3-2-4-12-13(9)17-14(18)10-7-8(16)5-6-11(10)21-12/h2-7H,1H3,(H,17,18)
InChI Key HGYAROLWFFFLIE-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10ClNO4
Molecular Weight 303.69 g/mol
Exact Mass 303.0298355 g/mol
Topological Polar Surface Area (TPSA) 64.60 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Mycemycin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 + 0.8285 82.85%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.5527 55.27%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9019 90.19%
OATP1B3 inhibitior + 0.9582 95.82%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7771 77.71%
P-glycoprotein inhibitior - 0.6891 68.91%
P-glycoprotein substrate - 0.8355 83.55%
CYP3A4 substrate + 0.6686 66.86%
CYP2C9 substrate - 0.5802 58.02%
CYP2D6 substrate - 0.8899 88.99%
CYP3A4 inhibition - 0.5773 57.73%
CYP2C9 inhibition - 0.5627 56.27%
CYP2C19 inhibition - 0.5947 59.47%
CYP2D6 inhibition - 0.9213 92.13%
CYP1A2 inhibition + 0.7397 73.97%
CYP2C8 inhibition + 0.5395 53.95%
CYP inhibitory promiscuity + 0.5157 51.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6818 68.18%
Carcinogenicity (trinary) Danger 0.4326 43.26%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.5573 55.73%
Skin irritation - 0.8527 85.27%
Skin corrosion - 0.9613 96.13%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6041 60.41%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.9081 90.81%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.6776 67.76%
Acute Oral Toxicity (c) III 0.6954 69.54%
Estrogen receptor binding + 0.8792 87.92%
Androgen receptor binding + 0.6454 64.54%
Thyroid receptor binding + 0.5636 56.36%
Glucocorticoid receptor binding + 0.8782 87.82%
Aromatase binding + 0.6453 64.53%
PPAR gamma + 0.8418 84.18%
Honey bee toxicity - 0.8961 89.61%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5109 51.09%
Fish aquatic toxicity + 0.9245 92.45%

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
CHEMBL240 Q12809 HERG 98.59% 89.76%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.92% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.76% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 94.83% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.97% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.90% 94.80%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.75% 94.00%
CHEMBL2581 P07339 Cathepsin D 91.59% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 91.10% 91.19%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.66% 96.09%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 89.49% 92.29%
CHEMBL4208 P20618 Proteasome component C5 88.83% 90.00%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 88.00% 83.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.71% 95.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.98% 95.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 86.17% 81.11%
CHEMBL2535 P11166 Glucose transporter 86.00% 98.75%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.95% 100.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.52% 94.42%
CHEMBL4530 P00488 Coagulation factor XIII 82.19% 96.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.95% 96.95%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.05% 93.03%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.04% 86.92%

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 139588622
LOTUS LTS0052307
wikiData Q105028069