Leopersin B

Details

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Internal ID f1863409-fb01-41b7-99d7-9763cd2b426d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name
SMILES (Canonical) CC(=O)OC1(C(=O)CC2C(CCCC2(C13CCC4(O3)CC(OC4)O)C)(C)C)C
SMILES (Isomeric) CC(=O)O[C@]1(C(=O)C[C@@H]2[C@@]([C@@]13CC[C@@]4(O3)C[C@H](OC4)O)(CCCC2(C)C)C)C
InChI InChI=1S/C22H34O6/c1-14(23)27-20(5)16(24)11-15-18(2,3)7-6-8-19(15,4)22(20)10-9-21(28-22)12-17(25)26-13-21/h15,17,25H,6-13H2,1-5H3/t15-,17-,19-,20-,21+,22-/m0/s1
InChI Key PYWYXDQVIHVOOS-YXJJOUJBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H34O6
Molecular Weight 394.50 g/mol
Exact Mass 394.23553880 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Leopersin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9762 97.62%
Caco-2 + 0.5897 58.97%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8481 84.81%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.8445 84.45%
OATP1B3 inhibitior + 0.8798 87.98%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5364 53.64%
BSEP inhibitior - 0.4777 47.77%
P-glycoprotein inhibitior - 0.6106 61.06%
P-glycoprotein substrate - 0.7748 77.48%
CYP3A4 substrate + 0.6578 65.78%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8677 86.77%
CYP3A4 inhibition - 0.7440 74.40%
CYP2C9 inhibition - 0.7367 73.67%
CYP2C19 inhibition - 0.8388 83.88%
CYP2D6 inhibition - 0.9684 96.84%
CYP1A2 inhibition - 0.8878 88.78%
CYP2C8 inhibition - 0.5842 58.42%
CYP inhibitory promiscuity - 0.9701 97.01%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5423 54.23%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.8628 86.28%
Skin irritation - 0.6017 60.17%
Skin corrosion - 0.9200 92.00%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6419 64.19%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.9159 91.59%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.7258 72.58%
Acute Oral Toxicity (c) III 0.3558 35.58%
Estrogen receptor binding + 0.8846 88.46%
Androgen receptor binding + 0.7332 73.32%
Thyroid receptor binding + 0.6249 62.49%
Glucocorticoid receptor binding + 0.7211 72.11%
Aromatase binding + 0.8162 81.62%
PPAR gamma + 0.6759 67.59%
Honey bee toxicity - 0.8175 81.75%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6150 61.50%
Fish aquatic toxicity + 0.9726 97.26%

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 97.71% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.68% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.65% 99.23%
CHEMBL2581 P07339 Cathepsin D 89.42% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.68% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.09% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.71% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.31% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.90% 95.56%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 83.56% 95.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.48% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.88% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 82.87% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.38% 89.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.69% 93.03%
CHEMBL340 P08684 Cytochrome P450 3A4 81.25% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.12% 92.94%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 81.04% 96.39%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.66% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.25% 82.69%

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.
Leonurus japonicus
Leonurus persicus

Cross-Links

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PubChem 101685533
NPASS NPC109688
LOTUS LTS0090137
wikiData Q105216826