5(S),9(S),10(S)-15,16-Epoxycleroda-3,8,13(16),14-tetraene-19,18:20,12(S)-diolactone (swassin)

Details

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Internal ID 93da0b02-f33d-4783-aa28-80ff6cf5f2a5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name (5'S,6aS,7S,10aS)-5'-(furan-3-yl)-8-methylidenespiro[1,5,6,6a,9,10-hexahydrobenzo[d][2]benzofuran-7,3'-oxolane]-2',3-dione
SMILES (Canonical) C=C1CCC23COC(=O)C2=CCCC3C14CC(OC4=O)C5=COC=C5
SMILES (Isomeric) C=C1CC[C@@]23COC(=O)C2=CCC[C@@H]3[C@@]14C[C@H](OC4=O)C5=COC=C5
InChI InChI=1S/C20H20O5/c1-12-5-7-19-11-24-17(21)14(19)3-2-4-16(19)20(12)9-15(25-18(20)22)13-6-8-23-10-13/h3,6,8,10,15-16H,1-2,4-5,7,9,11H2/t15-,16-,19+,20+/m0/s1
InChI Key WQEZWMOABWIAIU-XAMWDVODSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O5
Molecular Weight 340.40 g/mol
Exact Mass 340.13107373 g/mol
Topological Polar Surface Area (TPSA) 65.70 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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5(S),9(S),10(S)-15,16-Epoxycleroda-3,8,13(16),14-tetraene-19,18:20,12(S)-diolactone (swassin)

2D Structure

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2D Structure of 5(S),9(S),10(S)-15,16-Epoxycleroda-3,8,13(16),14-tetraene-19,18:20,12(S)-diolactone (swassin)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 - 0.5519 55.19%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8310 83.10%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.8665 86.65%
OATP1B3 inhibitior + 0.9306 93.06%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.5446 54.46%
P-glycoprotein inhibitior - 0.6285 62.85%
P-glycoprotein substrate - 0.7374 73.74%
CYP3A4 substrate + 0.6211 62.11%
CYP2C9 substrate - 0.8047 80.47%
CYP2D6 substrate - 0.8469 84.69%
CYP3A4 inhibition - 0.5394 53.94%
CYP2C9 inhibition - 0.6716 67.16%
CYP2C19 inhibition - 0.7290 72.90%
CYP2D6 inhibition - 0.8763 87.63%
CYP1A2 inhibition - 0.7709 77.09%
CYP2C8 inhibition + 0.5615 56.15%
CYP inhibitory promiscuity - 0.7213 72.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9243 92.43%
Carcinogenicity (trinary) Non-required 0.5224 52.24%
Eye corrosion - 0.9389 93.89%
Eye irritation - 0.8444 84.44%
Skin irritation - 0.7633 76.33%
Skin corrosion - 0.9478 94.78%
Ames mutagenesis - 0.6470 64.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8501 85.01%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.6302 63.02%
skin sensitisation - 0.7970 79.70%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.6459 64.59%
Acute Oral Toxicity (c) III 0.5318 53.18%
Estrogen receptor binding + 0.8162 81.62%
Androgen receptor binding + 0.6550 65.50%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6456 64.56%
Aromatase binding + 0.6431 64.31%
PPAR gamma + 0.5939 59.39%
Honey bee toxicity - 0.8081 80.81%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9934 99.34%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 94.73% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.25% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.69% 93.40%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.83% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.66% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.42% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.84% 100.00%
CHEMBL4530 P00488 Coagulation factor XIII 85.14% 96.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.71% 82.69%
CHEMBL221 P23219 Cyclooxygenase-1 82.43% 90.17%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 82.38% 82.05%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.83% 92.62%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.34% 93.04%

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.
Croton sublyratus

Cross-Links

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PubChem 91741938
LOTUS LTS0256201
wikiData Q104396717