Arsanin

Details

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Internal ID cc83e8b1-8adf-432b-8623-13d127e51578
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Eudesmanolides, secoeudesmanolides, and derivatives
IUPAC Name (3S,3aS,5aR,6R,9S,9aS,9bS)-6-hydroxy-3,5a,9-trimethyl-3a,4,5,6,7,9,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2,8-dione
SMILES (Canonical) CC1C2CCC3(C(CC(=O)C(C3C2OC1=O)C)O)C
SMILES (Isomeric) C[C@H]1[C@@H]2CC[C@]3([C@@H](CC(=O)[C@H]([C@@H]3[C@H]2OC1=O)C)O)C
InChI InChI=1S/C15H22O4/c1-7-9-4-5-15(3)11(17)6-10(16)8(2)12(15)13(9)19-14(7)18/h7-9,11-13,17H,4-6H2,1-3H3/t7-,8+,9-,11+,12+,13-,15-/m0/s1
InChI Key YRFWEPYMRLGVBZ-SNNRJATNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O4
Molecular Weight 266.33 g/mol
Exact Mass 266.15180918 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.55
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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41135-04-0

2D Structure

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2D Structure of Arsanin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9834 98.34%
Caco-2 + 0.7445 74.45%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7279 72.79%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.9020 90.20%
OATP1B3 inhibitior + 0.8757 87.57%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6571 65.71%
BSEP inhibitior - 0.9298 92.98%
P-glycoprotein inhibitior - 0.8403 84.03%
P-glycoprotein substrate - 0.8421 84.21%
CYP3A4 substrate + 0.6165 61.65%
CYP2C9 substrate - 0.8176 81.76%
CYP2D6 substrate - 0.8269 82.69%
CYP3A4 inhibition - 0.7224 72.24%
CYP2C9 inhibition - 0.8834 88.34%
CYP2C19 inhibition - 0.8858 88.58%
CYP2D6 inhibition - 0.9784 97.84%
CYP1A2 inhibition - 0.7894 78.94%
CYP2C8 inhibition - 0.9346 93.46%
CYP inhibitory promiscuity - 0.9877 98.77%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6210 62.10%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.9497 94.97%
Skin irritation + 0.6426 64.26%
Skin corrosion - 0.7711 77.11%
Ames mutagenesis - 0.7070 70.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5856 58.56%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.6908 69.08%
skin sensitisation - 0.8907 89.07%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity + 0.5543 55.43%
Acute Oral Toxicity (c) III 0.3465 34.65%
Estrogen receptor binding + 0.8019 80.19%
Androgen receptor binding + 0.6446 64.46%
Thyroid receptor binding + 0.6290 62.90%
Glucocorticoid receptor binding + 0.5474 54.74%
Aromatase binding - 0.7440 74.40%
PPAR gamma - 0.6765 67.65%
Honey bee toxicity - 0.8322 83.22%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9760 97.60%

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 92.32% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.40% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.39% 96.77%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.82% 100.00%
CHEMBL2581 P07339 Cathepsin D 85.51% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.41% 95.56%
CHEMBL1902 P62942 FK506-binding protein 1A 84.96% 97.05%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.66% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.50% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.31% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.22% 89.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.31% 93.04%
CHEMBL1871 P10275 Androgen Receptor 82.27% 96.43%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.51% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.18% 95.89%

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.
Artemisia arborescens
Taraxacum mongolicum

Cross-Links

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PubChem 13864723
NPASS NPC206046
LOTUS LTS0048362
wikiData Q105352775