Lycoposerramine-M

Details

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Internal ID b8091b59-d2d2-4050-b76b-eee01e39eb97
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,2R,3S,10S,13S,15R)-3-hydroxy-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadecan-11-one
SMILES (Canonical) CC1CC2CC(=O)C3CCCN4C3(C1)C2C(CC4)O
SMILES (Isomeric) C[C@@H]1C[C@H]2CC(=O)[C@H]3CCCN4[C@]3(C1)[C@@H]2[C@H](CC4)O
InChI InChI=1S/C16H25NO2/c1-10-7-11-8-14(19)12-3-2-5-17-6-4-13(18)15(11)16(12,17)9-10/h10-13,15,18H,2-9H2,1H3/t10-,11+,12-,13+,15+,16+/m1/s1
InChI Key QPVQGYVJKIXZFG-GMCZJSKOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H25NO2
Molecular Weight 263.37 g/mol
Exact Mass 263.188529040 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.84
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Lycoposerramine-M

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.8030 80.30%
Blood Brain Barrier + 0.9129 91.29%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.4793 47.93%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.9083 90.83%
OATP1B3 inhibitior + 0.9519 95.19%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.7307 73.07%
P-glycoprotein inhibitior - 0.9206 92.06%
P-glycoprotein substrate - 0.6184 61.84%
CYP3A4 substrate + 0.5521 55.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4705 47.05%
CYP3A4 inhibition - 0.6678 66.78%
CYP2C9 inhibition - 0.8874 88.74%
CYP2C19 inhibition - 0.9221 92.21%
CYP2D6 inhibition - 0.6143 61.43%
CYP1A2 inhibition - 0.9321 93.21%
CYP2C8 inhibition - 0.9187 91.87%
CYP inhibitory promiscuity - 0.9901 99.01%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5289 52.89%
Eye corrosion - 0.9817 98.17%
Eye irritation - 0.7296 72.96%
Skin irritation - 0.6398 63.98%
Skin corrosion - 0.7424 74.24%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6104 61.04%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8137 81.37%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.5703 57.03%
Acute Oral Toxicity (c) III 0.6827 68.27%
Estrogen receptor binding - 0.5461 54.61%
Androgen receptor binding + 0.6447 64.47%
Thyroid receptor binding + 0.5179 51.79%
Glucocorticoid receptor binding + 0.6053 60.53%
Aromatase binding - 0.6931 69.31%
PPAR gamma - 0.8061 80.61%
Honey bee toxicity - 0.9002 90.02%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity - 0.9087 90.87%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.79% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.64% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.29% 97.09%
CHEMBL2581 P07339 Cathepsin D 92.89% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.15% 92.94%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 88.24% 95.58%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.53% 95.89%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.99% 93.04%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 85.83% 94.78%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.13% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.97% 95.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.27% 93.03%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.24% 86.33%
CHEMBL217 P14416 Dopamine D2 receptor 83.19% 95.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.79% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.60% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.88% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.41% 89.00%

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.
Huperzia serrata
Lycopodium japonicum

Cross-Links

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PubChem 11129147
NPASS NPC157935
LOTUS LTS0171915
wikiData Q105225625