Armatin D

Details

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Internal ID 6bf60027-542b-4c74-99c3-76ed7da0b485
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,2R,3aS,7S,9S,9aS,9bR)-2-methoxy-1,9,9a-trimethyl-2,3a,4,5,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran-7-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H26O3/c1-9-7-12(17)8-11-5-6-13-14(16(9,11)3)10(2)15(18-4)19-13/h8-10,12-15,17H,5-7H2,1-4H3/t9-,10-,12-,13-,14-,15+,16+/m0/s1
InChI Key RVIFTQUMZYSBBG-XBNBVDRNSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H26O3
Molecular Weight 266.38 g/mol
Exact Mass 266.18819469 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.74
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL455764

2D Structure

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2D Structure of Armatin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.8601 86.01%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.5521 55.21%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.8877 88.77%
OATP1B3 inhibitior + 0.9628 96.28%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.8453 84.53%
P-glycoprotein inhibitior - 0.8414 84.14%
P-glycoprotein substrate - 0.7635 76.35%
CYP3A4 substrate + 0.6396 63.96%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7707 77.07%
CYP3A4 inhibition - 0.6699 66.99%
CYP2C9 inhibition - 0.8082 80.82%
CYP2C19 inhibition - 0.7498 74.98%
CYP2D6 inhibition - 0.9028 90.28%
CYP1A2 inhibition + 0.5191 51.91%
CYP2C8 inhibition - 0.5677 56.77%
CYP inhibitory promiscuity - 0.7376 73.76%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4870 48.70%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9544 95.44%
Skin irritation + 0.5162 51.62%
Skin corrosion - 0.9224 92.24%
Ames mutagenesis - 0.7154 71.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4476 44.76%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.5303 53.03%
skin sensitisation - 0.7502 75.02%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.5586 55.86%
Acute Oral Toxicity (c) III 0.5793 57.93%
Estrogen receptor binding - 0.6315 63.15%
Androgen receptor binding + 0.5220 52.20%
Thyroid receptor binding + 0.6221 62.21%
Glucocorticoid receptor binding - 0.5269 52.69%
Aromatase binding - 0.7096 70.96%
PPAR gamma - 0.6379 63.79%
Honey bee toxicity - 0.7648 76.48%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9293 92.93%

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 98.08% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 94.90% 92.94%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.61% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.26% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.66% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.50% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 86.48% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.02% 95.89%
CHEMBL1871 P10275 Androgen Receptor 85.51% 96.43%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.84% 97.25%
CHEMBL2996 Q05655 Protein kinase C delta 80.67% 97.79%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.57% 94.00%

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 11184702
LOTUS LTS0016275
wikiData Q105246052