Myrocin B

Details

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Internal ID 23fee665-4d85-4c54-813a-039be93f497c
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name (1S,2S,5R,9S,12S,15S,17R)-5-ethenyl-2,9-dihydroxy-5,12-dimethyl-10-oxapentacyclo[7.7.1.01,15.02,7.012,17]heptadec-6-ene-3,8,11-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H22O6/c1-4-16(2)8-11-13(22)20(25)14-17(3,15(23)26-20)6-5-10-7-18(10,14)19(11,24)12(21)9-16/h4,8,10,14,24-25H,1,5-7,9H2,2-3H3/t10-,14-,16+,17-,18-,19-,20+/m0/s1
InChI Key ZALWBYOUGDMNTP-RXSCCBSPSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H22O6
Molecular Weight 358.40 g/mol
Exact Mass 358.14163842 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.06
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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(1S,2S,5R,9S,12S,15S,17R)-5-Ethenyl-2,9-dihydroxy-5,12-dimethyl-10-oxapentacyclo[7.7.1.01,15.02,7.012,17]heptadec-6-ene-3,8,11-trione

2D Structure

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2D Structure of Myrocin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9815 98.15%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7784 77.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9139 91.39%
OATP1B3 inhibitior + 0.8933 89.33%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5124 51.24%
BSEP inhibitior - 0.4772 47.72%
P-glycoprotein inhibitior - 0.8162 81.62%
P-glycoprotein substrate - 0.8506 85.06%
CYP3A4 substrate + 0.6389 63.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8845 88.45%
CYP3A4 inhibition - 0.6479 64.79%
CYP2C9 inhibition - 0.7826 78.26%
CYP2C19 inhibition - 0.8576 85.76%
CYP2D6 inhibition - 0.9384 93.84%
CYP1A2 inhibition + 0.5333 53.33%
CYP2C8 inhibition + 0.4895 48.95%
CYP inhibitory promiscuity - 0.9194 91.94%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.4945 49.45%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9633 96.33%
Skin irritation + 0.5455 54.55%
Skin corrosion - 0.8854 88.54%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5791 57.91%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.6408 64.08%
skin sensitisation - 0.8191 81.91%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.7975 79.75%
Acute Oral Toxicity (c) IV 0.3648 36.48%
Estrogen receptor binding + 0.6162 61.62%
Androgen receptor binding + 0.6842 68.42%
Thyroid receptor binding + 0.5903 59.03%
Glucocorticoid receptor binding + 0.6770 67.70%
Aromatase binding + 0.6780 67.80%
PPAR gamma - 0.5972 59.72%
Honey bee toxicity - 0.8903 89.03%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 1.0000 100.00%

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 93.70% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.09% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.41% 95.56%
CHEMBL240 Q12809 HERG 89.30% 89.76%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.27% 97.09%
CHEMBL1951 P21397 Monoamine oxidase A 85.96% 91.49%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.80% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 82.05% 94.75%
CHEMBL2581 P07339 Cathepsin D 81.78% 98.95%

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 14059869
LOTUS LTS0032939
wikiData Q77370867