Myrislignan

Details

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Internal ID a2f09a7f-f879-4226-bdd9-89a47e9543bb
Taxonomy Lignans, neolignans and related compounds
IUPAC Name 4-[(1R,2S)-2-(2,6-dimethoxy-4-prop-2-enylphenoxy)-1-hydroxypropyl]-2-methoxyphenol
SMILES (Canonical) CC(C(C1=CC(=C(C=C1)O)OC)O)OC2=C(C=C(C=C2OC)CC=C)OC
SMILES (Isomeric) C[C@@H]([C@@H](C1=CC(=C(C=C1)O)OC)O)OC2=C(C=C(C=C2OC)CC=C)OC
InChI InChI=1S/C21H26O6/c1-6-7-14-10-18(25-4)21(19(11-14)26-5)27-13(2)20(23)15-8-9-16(22)17(12-15)24-3/h6,8-13,20,22-23H,1,7H2,2-5H3/t13-,20-/m0/s1
InChI Key ULZFTGWWPHYLGI-RBZFPXEDSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C21H26O6
Molecular Weight 374.40 g/mol
Exact Mass 374.17293854 g/mol
Topological Polar Surface Area (TPSA) 77.40 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.65
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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171485-39-5
CHEMBL4085435
(aR)-alpha-[(1S)-1-[2,6-Dimethoxy-4-(2-propen-1-yl)phenoxy]ethyl]-4-hydroxy-3-methoxybenzenemethanol
(-)-(1R,2S)-Myrislignan
DTXSID30333494
HY-N0608
BDBM50242967
MFCD13195532
s3261
AKOS015909818
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Myrislignan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9770 97.70%
Caco-2 + 0.6271 62.71%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7134 71.34%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.8588 85.88%
OATP1B3 inhibitior + 0.9164 91.64%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6193 61.93%
P-glycoprotein inhibitior - 0.4788 47.88%
P-glycoprotein substrate - 0.6494 64.94%
CYP3A4 substrate - 0.5285 52.85%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate + 0.4432 44.32%
CYP3A4 inhibition + 0.6497 64.97%
CYP2C9 inhibition - 0.6898 68.98%
CYP2C19 inhibition + 0.7508 75.08%
CYP2D6 inhibition - 0.7093 70.93%
CYP1A2 inhibition + 0.6970 69.70%
CYP2C8 inhibition + 0.5361 53.61%
CYP inhibitory promiscuity + 0.8079 80.79%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7621 76.21%
Carcinogenicity (trinary) Non-required 0.6612 66.12%
Eye corrosion - 0.9712 97.12%
Eye irritation - 0.8637 86.37%
Skin irritation - 0.8198 81.98%
Skin corrosion - 0.8954 89.54%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4608 46.08%
Micronuclear + 0.5259 52.59%
Hepatotoxicity - 0.5057 50.57%
skin sensitisation - 0.7041 70.41%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.8480 84.80%
Acute Oral Toxicity (c) III 0.6856 68.56%
Estrogen receptor binding + 0.7585 75.85%
Androgen receptor binding - 0.6049 60.49%
Thyroid receptor binding + 0.7490 74.90%
Glucocorticoid receptor binding + 0.7495 74.95%
Aromatase binding + 0.6279 62.79%
PPAR gamma - 0.5098 50.98%
Honey bee toxicity - 0.8700 87.00%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9906 99.06%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.72% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.65% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.56% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.44% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.19% 94.45%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 93.17% 89.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.77% 99.17%
CHEMBL4208 P20618 Proteasome component C5 92.01% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 91.20% 90.20%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.21% 99.15%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.41% 90.24%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.01% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.52% 86.33%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.45% 95.89%
CHEMBL2535 P11166 Glucose transporter 82.77% 98.75%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.92% 95.17%

Plants that contains it

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Cross-Links

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PubChem 21636106
NPASS NPC203831
LOTUS LTS0228300
wikiData Q105275431