Myricananin B

Details

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Internal ID 4a076c10-9665-44dc-99c2-da594fdbd836
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name (8S,12S)-19,20-dimethoxy-10,10-dimethyl-9,11-dioxatetracyclo[15.3.1.12,6.08,12]docosa-1(20),2,4,6(22),17(21),18-hexaene-3,18-diol
SMILES (Canonical) CC1(OC2CCCCC3=CC(=C(C(=C3O)OC)OC)C4=C(C=CC(=C4)CC2O1)O)C
SMILES (Isomeric) CC1(O[C@H]2CCCCC3=CC(=C(C(=C3O)OC)OC)C4=C(C=CC(=C4)C[C@@H]2O1)O)C
InChI InChI=1S/C24H30O6/c1-24(2)29-19-8-6-5-7-15-13-17(22(27-3)23(28-4)21(15)26)16-11-14(9-10-18(16)25)12-20(19)30-24/h9-11,13,19-20,25-26H,5-8,12H2,1-4H3/t19-,20-/m0/s1
InChI Key LGOUSRFEXBDUON-PMACEKPBSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C24H30O6
Molecular Weight 414.50 g/mol
Exact Mass 414.20423867 g/mol
Topological Polar Surface Area (TPSA) 77.40 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.57
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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CHEMBL523109

2D Structure

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2D Structure of Myricananin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9076 90.76%
Caco-2 + 0.7414 74.14%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8309 83.09%
OATP2B1 inhibitior - 0.8627 86.27%
OATP1B1 inhibitior + 0.8840 88.40%
OATP1B3 inhibitior + 0.8375 83.75%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6821 68.21%
BSEP inhibitior + 0.8957 89.57%
P-glycoprotein inhibitior - 0.4634 46.34%
P-glycoprotein substrate - 0.5889 58.89%
CYP3A4 substrate + 0.6148 61.48%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate + 0.3759 37.59%
CYP3A4 inhibition - 0.6873 68.73%
CYP2C9 inhibition - 0.7131 71.31%
CYP2C19 inhibition - 0.5409 54.09%
CYP2D6 inhibition - 0.8636 86.36%
CYP1A2 inhibition + 0.5880 58.80%
CYP2C8 inhibition + 0.6840 68.40%
CYP inhibitory promiscuity - 0.6341 63.41%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.4105 41.05%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9049 90.49%
Skin irritation - 0.8034 80.34%
Skin corrosion - 0.9454 94.54%
Ames mutagenesis - 0.5454 54.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6591 65.91%
Micronuclear - 0.6200 62.00%
Hepatotoxicity - 0.5042 50.42%
skin sensitisation - 0.8749 87.49%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.8458 84.58%
Acute Oral Toxicity (c) III 0.3675 36.75%
Estrogen receptor binding + 0.8449 84.49%
Androgen receptor binding + 0.7935 79.35%
Thyroid receptor binding + 0.7851 78.51%
Glucocorticoid receptor binding + 0.8719 87.19%
Aromatase binding + 0.8161 81.61%
PPAR gamma + 0.6950 69.50%
Honey bee toxicity - 0.8721 87.21%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9766 97.66%

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 99.78% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.00% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 95.12% 92.94%
CHEMBL1951 P21397 Monoamine oxidase A 94.88% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.20% 95.89%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 91.20% 92.88%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.36% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.26% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.51% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.46% 92.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.87% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.09% 95.56%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 86.99% 96.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 86.40% 91.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.70% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.56% 94.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.80% 93.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.53% 99.15%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 82.34% 91.79%
CHEMBL2535 P11166 Glucose transporter 80.39% 98.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Myrica nana

Cross-Links

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PubChem 44579910
NPASS NPC41782
LOTUS LTS0191716
wikiData Q105151498