MyricaneneB

Details

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Internal ID 92204b46-cb0f-440c-af9c-437a5f896e55
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Cyclic diarylheptanoids > Meta,meta-bridged biphenyls
IUPAC Name (8Z)-16,17-dimethoxytricyclo[12.3.1.12,6]nonadeca-1(17),2,4,6(19),8,14(18),15-heptaene-3,15-diol
SMILES (Canonical) COC1=C2C=C(CCCCC=CCC3=CC2=C(C=C3)O)C(=C1OC)O
SMILES (Isomeric) COC1=C2C=C(CCCC/C=C\CC3=CC2=C(C=C3)O)C(=C1OC)O
InChI InChI=1S/C21H24O4/c1-24-20-17-13-15(19(23)21(20)25-2)9-7-5-3-4-6-8-14-10-11-18(22)16(17)12-14/h4,6,10-13,22-23H,3,5,7-9H2,1-2H3/b6-4-
InChI Key JKMZSGSRYKMBOO-XQRVVYSFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H24O4
Molecular Weight 340.40 g/mol
Exact Mass 340.16745924 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.61
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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SCHEMBL15326614

2D Structure

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2D Structure of MyricaneneB

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9837 98.37%
Caco-2 + 0.7542 75.42%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8223 82.23%
OATP2B1 inhibitior - 0.8511 85.11%
OATP1B1 inhibitior + 0.8722 87.22%
OATP1B3 inhibitior + 0.9632 96.32%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.7571 75.71%
BSEP inhibitior + 0.8143 81.43%
P-glycoprotein inhibitior - 0.5109 51.09%
P-glycoprotein substrate - 0.7934 79.34%
CYP3A4 substrate + 0.5382 53.82%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate + 0.4452 44.52%
CYP3A4 inhibition - 0.6565 65.65%
CYP2C9 inhibition - 0.6454 64.54%
CYP2C19 inhibition + 0.6051 60.51%
CYP2D6 inhibition - 0.7999 79.99%
CYP1A2 inhibition + 0.9523 95.23%
CYP2C8 inhibition + 0.5238 52.38%
CYP inhibitory promiscuity + 0.5425 54.25%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8063 80.63%
Carcinogenicity (trinary) Non-required 0.5808 58.08%
Eye corrosion - 0.9831 98.31%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.6876 68.76%
Skin corrosion - 0.9035 90.35%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6891 68.91%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.6467 64.67%
skin sensitisation - 0.7695 76.95%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8752 87.52%
Acute Oral Toxicity (c) III 0.5261 52.61%
Estrogen receptor binding + 0.8148 81.48%
Androgen receptor binding + 0.6473 64.73%
Thyroid receptor binding + 0.7279 72.79%
Glucocorticoid receptor binding + 0.8026 80.26%
Aromatase binding + 0.6372 63.72%
PPAR gamma + 0.8409 84.09%
Honey bee toxicity - 0.8991 89.91%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9931 99.31%

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 99.41% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.19% 91.49%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.54% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.24% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.19% 98.95%
CHEMBL4208 P20618 Proteasome component C5 91.77% 90.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 90.00% 91.79%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.18% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.50% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.13% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.37% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.64% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.81% 95.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.63% 92.94%
CHEMBL2535 P11166 Glucose transporter 82.01% 98.75%
CHEMBL2056 P21728 Dopamine D1 receptor 81.46% 91.00%

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 rubra

Cross-Links

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PubChem 89856897
NPASS NPC180062