Serratidine

Details

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Internal ID 9584657f-580b-4f79-bd4b-f257862e1207
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,10S,13R)-13-hydroxy-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadec-2-en-11-one
SMILES (Canonical) CC1CC2(CC(=O)C3CCCN4C3(C1)C2=CCC4)O
SMILES (Isomeric) CC1C[C@]2(CC(=O)[C@H]3CCCN4[C@]3(C1)C2=CCC4)O
InChI InChI=1S/C16H23NO2/c1-11-8-15(19)10-13(18)12-4-2-6-17-7-3-5-14(15)16(12,17)9-11/h5,11-12,19H,2-4,6-10H2,1H3/t11?,12-,15-,16+/m1/s1
InChI Key SEWDNOQXMYWSRQ-ARQBPDDDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H23NO2
Molecular Weight 261.36 g/mol
Exact Mass 261.172878976 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.90
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 Serratidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 + 0.8994 89.94%
Blood Brain Barrier + 0.8557 85.57%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5360 53.60%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.9485 94.85%
OATP1B3 inhibitior + 0.9569 95.69%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.5444 54.44%
P-glycoprotein inhibitior - 0.9309 93.09%
P-glycoprotein substrate - 0.7106 71.06%
CYP3A4 substrate + 0.5293 52.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3721 37.21%
CYP3A4 inhibition - 0.8959 89.59%
CYP2C9 inhibition - 0.8923 89.23%
CYP2C19 inhibition - 0.8756 87.56%
CYP2D6 inhibition - 0.7245 72.45%
CYP1A2 inhibition - 0.8882 88.82%
CYP2C8 inhibition - 0.9313 93.13%
CYP inhibitory promiscuity - 0.9731 97.31%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4204 42.04%
Eye corrosion - 0.9813 98.13%
Eye irritation - 0.7926 79.26%
Skin irritation - 0.6805 68.05%
Skin corrosion - 0.8469 84.69%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5677 56.77%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.7811 78.11%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity + 0.7019 70.19%
Acute Oral Toxicity (c) III 0.6931 69.31%
Estrogen receptor binding - 0.7814 78.14%
Androgen receptor binding - 0.5201 52.01%
Thyroid receptor binding + 0.5392 53.92%
Glucocorticoid receptor binding - 0.4929 49.29%
Aromatase binding - 0.6817 68.17%
PPAR gamma - 0.7057 70.57%
Honey bee toxicity - 0.9461 94.61%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity - 0.7390 73.90%

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 98.68% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.99% 91.11%
CHEMBL4208 P20618 Proteasome component C5 91.76% 90.00%
CHEMBL2581 P07339 Cathepsin D 91.66% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.51% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.00% 95.56%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.48% 92.94%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 88.71% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.68% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.27% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.61% 100.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.35% 86.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 84.94% 90.24%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.49% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.72% 89.00%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 82.62% 94.78%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.04% 96.77%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.35% 85.14%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.14% 93.03%

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 selago
Huperzia serrata

Cross-Links

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PubChem 20056306
LOTUS LTS0117204
wikiData Q105251565