Lolicine-B 11-O-propionate

Details

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Internal ID 923686c8-af12-46da-995d-11e704d37b9f
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Oxosteroids > 19-oxosteroids
IUPAC Name [(2S,3S,6S,8S,10R,11R,12R,15S,21R,25R)-11-formyl-8-(2-hydroxypropan-2-yl)-2,3,22,22,24,24-hexamethyl-26-oxo-7,23-dioxa-31-azaoctacyclo[15.14.0.02,15.03,12.06,11.018,30.019,27.021,25]hentriaconta-1(17),18(30),19(27),28-tetraen-10-yl] propanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C41H55NO7/c1-10-31(44)48-30-19-29(36(2,3)46)47-28-15-16-39(8)27(41(28,30)20-43)14-11-21-17-24-32-23-18-25-33(38(6,7)49-37(25,4)5)34(45)22(23)12-13-26(32)42-35(24)40(21,39)9/h12-13,20-21,25,27-30,33,42,46H,10-11,14-19H2,1-9H3/t21-,25+,27+,28-,29-,30+,33-,39-,40+,41-/m0/s1
InChI Key PUDUYGKIVHTRTL-SKACZCJFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C41H55NO7
Molecular Weight 673.90 g/mol
Exact Mass 673.39785309 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 6.80
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Lolicine-B 11-O-propionate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9588 95.88%
Caco-2 - 0.8023 80.23%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6775 67.75%
OATP2B1 inhibitior - 0.7152 71.52%
OATP1B1 inhibitior + 0.7945 79.45%
OATP1B3 inhibitior + 0.8105 81.05%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9946 99.46%
P-glycoprotein inhibitior + 0.8267 82.67%
P-glycoprotein substrate + 0.7382 73.82%
CYP3A4 substrate + 0.7408 74.08%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.8714 87.14%
CYP3A4 inhibition - 0.6516 65.16%
CYP2C9 inhibition - 0.8380 83.80%
CYP2C19 inhibition - 0.7906 79.06%
CYP2D6 inhibition - 0.9294 92.94%
CYP1A2 inhibition - 0.5528 55.28%
CYP2C8 inhibition + 0.8272 82.72%
CYP inhibitory promiscuity - 0.6141 61.41%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6040 60.40%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.9216 92.16%
Skin irritation - 0.7723 77.23%
Skin corrosion - 0.9333 93.33%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6963 69.63%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.8847 88.47%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.6047 60.47%
Acute Oral Toxicity (c) III 0.5603 56.03%
Estrogen receptor binding + 0.7629 76.29%
Androgen receptor binding + 0.7411 74.11%
Thyroid receptor binding + 0.5694 56.94%
Glucocorticoid receptor binding + 0.8138 81.38%
Aromatase binding + 0.6888 68.88%
PPAR gamma + 0.7164 71.64%
Honey bee toxicity - 0.7298 72.98%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9883 98.83%

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 99.39% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.67% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.32% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.98% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.87% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.76% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.30% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.12% 97.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 92.12% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.29% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.40% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 88.83% 97.79%
CHEMBL3922 P50579 Methionine aminopeptidase 2 87.80% 97.28%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.60% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.58% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.89% 86.33%
CHEMBL1902 P62942 FK506-binding protein 1A 86.78% 97.05%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 86.20% 95.71%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 86.03% 91.71%
CHEMBL2413 P32246 C-C chemokine receptor type 1 84.22% 89.50%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 83.69% 80.96%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.46% 85.11%
CHEMBL233 P35372 Mu opioid receptor 83.42% 97.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.57% 99.17%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.10% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.06% 89.34%
CHEMBL340 P08684 Cytochrome P450 3A4 80.80% 91.19%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.64% 97.50%

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 139583195
LOTUS LTS0251681
wikiData Q75056921