Maristachone D

Details

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Internal ID 91a8e2d1-a3af-40cd-b949-94e1c8a3d0b9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name (1R,3R)-5-(3,7-dimethylocta-2,6-dienoxy)-1,3,7-trimethoxy-3,6-dimethyl-1H-2-benzofuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H34O5/c1-15(2)10-9-11-16(3)12-13-27-19-14-18-20(21(24-6)17(19)4)22(25-7)28-23(18,5)26-8/h10,12,14,22H,9,11,13H2,1-8H3/t22-,23-/m1/s1
InChI Key NUMMDABPEFZWBV-DHIUTWEWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H34O5
Molecular Weight 390.50 g/mol
Exact Mass 390.24062418 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 5.00
Atomic LogP (AlogP) 5.57
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Maristachone D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.8349 83.49%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7159 71.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8532 85.32%
OATP1B3 inhibitior + 0.9466 94.66%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9254 92.54%
P-glycoprotein inhibitior + 0.8297 82.97%
P-glycoprotein substrate - 0.5826 58.26%
CYP3A4 substrate + 0.6092 60.92%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate + 0.3848 38.48%
CYP3A4 inhibition + 0.7325 73.25%
CYP2C9 inhibition + 0.5483 54.83%
CYP2C19 inhibition + 0.7040 70.40%
CYP2D6 inhibition - 0.7835 78.35%
CYP1A2 inhibition + 0.8657 86.57%
CYP2C8 inhibition + 0.6967 69.67%
CYP inhibitory promiscuity + 0.7570 75.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6387 63.87%
Eye corrosion - 0.9843 98.43%
Eye irritation - 0.8697 86.97%
Skin irritation - 0.8193 81.93%
Skin corrosion - 0.9669 96.69%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8145 81.45%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7231 72.31%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.5714 57.14%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.8087 80.87%
Acute Oral Toxicity (c) III 0.4415 44.15%
Estrogen receptor binding + 0.7825 78.25%
Androgen receptor binding + 0.6750 67.50%
Thyroid receptor binding + 0.7992 79.92%
Glucocorticoid receptor binding + 0.8347 83.47%
Aromatase binding + 0.6710 67.10%
PPAR gamma + 0.7863 78.63%
Honey bee toxicity - 0.7903 79.03%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5200 52.00%
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 98.07% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.53% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.48% 99.17%
CHEMBL2039 P27338 Monoamine oxidase B 93.13% 92.51%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.59% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 91.57% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.19% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.87% 94.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.45% 90.24%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.23% 92.08%
CHEMBL1937 Q92769 Histone deacetylase 2 84.10% 94.75%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 83.87% 91.03%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.82% 96.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.51% 92.94%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.53% 85.14%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.80% 95.89%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.47% 96.95%

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 139588467
LOTUS LTS0089617
wikiData Q105185941