Huperzine E

Details

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Internal ID 71273134-057f-4d93-860d-8c2de159409d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,2R,13S,15R)-11-hydroxy-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadeca-8,10-dien-12-one
SMILES (Canonical) CC1CC2C3CCCN4C3(C1)C(=C(C2=O)O)C=CC4
SMILES (Isomeric) C[C@@H]1C[C@H]2[C@H]3CCCN4[C@@]3(C1)C(=C(C2=O)O)C=CC4
InChI InChI=1S/C16H21NO2/c1-10-8-11-12-4-2-6-17-7-3-5-13(15(19)14(11)18)16(12,17)9-10/h3,5,10-12,19H,2,4,6-9H2,1H3/t10-,11+,12-,16-/m1/s1
InChI Key IRBNEBXOQHDOSE-AZKPJATDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H21NO2
Molecular Weight 259.34 g/mol
Exact Mass 259.157228913 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.45
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 Huperzine E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9805 98.05%
Caco-2 + 0.8876 88.76%
Blood Brain Barrier + 0.8629 86.29%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6931 69.31%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.9027 90.27%
OATP1B3 inhibitior + 0.9544 95.44%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.6981 69.81%
P-glycoprotein inhibitior - 0.9433 94.33%
P-glycoprotein substrate - 0.6865 68.65%
CYP3A4 substrate + 0.5943 59.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7824 78.24%
CYP3A4 inhibition - 0.8389 83.89%
CYP2C9 inhibition - 0.7864 78.64%
CYP2C19 inhibition - 0.8674 86.74%
CYP2D6 inhibition - 0.7097 70.97%
CYP1A2 inhibition - 0.7608 76.08%
CYP2C8 inhibition - 0.8737 87.37%
CYP inhibitory promiscuity - 0.8929 89.29%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4567 45.67%
Eye corrosion - 0.9807 98.07%
Eye irritation - 0.9399 93.99%
Skin irritation - 0.6594 65.94%
Skin corrosion - 0.8673 86.73%
Ames mutagenesis - 0.6278 62.78%
Human Ether-a-go-go-Related Gene inhibition - 0.6008 60.08%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.6369 63.69%
skin sensitisation - 0.7806 78.06%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.6013 60.13%
Acute Oral Toxicity (c) III 0.6165 61.65%
Estrogen receptor binding - 0.7273 72.73%
Androgen receptor binding + 0.6143 61.43%
Thyroid receptor binding - 0.5299 52.99%
Glucocorticoid receptor binding + 0.5807 58.07%
Aromatase binding - 0.7207 72.07%
PPAR gamma - 0.5483 54.83%
Honey bee toxicity - 0.9277 92.77%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.4285 42.85%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.56% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.20% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.19% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.02% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.47% 97.09%
CHEMBL2581 P07339 Cathepsin D 89.16% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.15% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.06% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.39% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.11% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.73% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.69% 95.89%
CHEMBL4208 P20618 Proteasome component C5 83.60% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.49% 89.00%
CHEMBL1871 P10275 Androgen Receptor 82.93% 96.43%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.50% 93.04%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.27% 86.33%

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.
Lycopodium japonicum

Cross-Links

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PubChem 102588705
NPASS NPC118514