Sampsonione L

Details

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Internal ID 342868c3-6e8c-408a-a185-4df7ddaa77ac
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 8-benzoyl-3-(2-hydroxypropan-2-yl)-9,9-dimethyl-6,10-bis(3-methylbut-2-enyl)-4-oxatricyclo[6.3.1.01,5]dodec-5-ene-7,12-dione
SMILES (Canonical) CC(=CCC1CC23CC(OC2=C(C(=O)C(C3=O)(C1(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C(C)(C)O)C
SMILES (Isomeric) CC(=CCC1CC23CC(OC2=C(C(=O)C(C3=O)(C1(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C(C)(C)O)C
InChI InChI=1S/C33H42O5/c1-20(2)14-16-23-18-32-19-25(31(7,8)37)38-28(32)24(17-15-21(3)4)27(35)33(29(32)36,30(23,5)6)26(34)22-12-10-9-11-13-22/h9-15,23,25,37H,16-19H2,1-8H3
InChI Key HDUWARMIHZANDI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C33H42O5
Molecular Weight 518.70 g/mol
Exact Mass 518.30322444 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 6.80
Atomic LogP (AlogP) 6.57
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Sampsonione L

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.6558 65.58%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7891 78.91%
OATP2B1 inhibitior - 0.8494 84.94%
OATP1B1 inhibitior + 0.8794 87.94%
OATP1B3 inhibitior + 0.8440 84.40%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9745 97.45%
P-glycoprotein inhibitior + 0.7432 74.32%
P-glycoprotein substrate - 0.5775 57.75%
CYP3A4 substrate + 0.6323 63.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8258 82.58%
CYP3A4 inhibition - 0.8514 85.14%
CYP2C9 inhibition - 0.6621 66.21%
CYP2C19 inhibition - 0.7460 74.60%
CYP2D6 inhibition - 0.9019 90.19%
CYP1A2 inhibition - 0.6978 69.78%
CYP2C8 inhibition + 0.5490 54.90%
CYP inhibitory promiscuity - 0.5832 58.32%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5170 51.70%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8705 87.05%
Skin irritation - 0.6192 61.92%
Skin corrosion - 0.9217 92.17%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4145 41.45%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.6419 64.19%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6445 64.45%
Acute Oral Toxicity (c) III 0.4929 49.29%
Estrogen receptor binding + 0.7754 77.54%
Androgen receptor binding + 0.6338 63.38%
Thyroid receptor binding + 0.6169 61.69%
Glucocorticoid receptor binding + 0.7182 71.82%
Aromatase binding + 0.7287 72.87%
PPAR gamma + 0.7019 70.19%
Honey bee toxicity - 0.8670 86.70%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9898 98.98%

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
CHEMBL221 P23219 Cyclooxygenase-1 97.80% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.78% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.68% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.96% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.76% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 90.61% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.28% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.34% 98.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.33% 91.07%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.30% 93.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 84.84% 95.71%
CHEMBL5028 O14672 ADAM10 84.26% 97.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.53% 89.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.38% 89.34%

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.
Hypericum sampsonii
Hypericum scabrum

Cross-Links

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PubChem 73797640
LOTUS LTS0039851
wikiData Q105026575