Methyl 3-(1-methyl-14-propan-2-yl-12-azatetracyclo[8.6.0.02,13.03,7]hexadec-3-en-2-yl)propanoate

Details

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Internal ID 6bce8163-3817-4b50-aea1-f34d7b8e98d3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name methyl 3-(1-methyl-14-propan-2-yl-12-azatetracyclo[8.6.0.02,13.03,7]hexadec-3-en-2-yl)propanoate
SMILES (Canonical) CC(C)C1CCC2(C3CCC4CCC=C4C2(C1NC3)CCC(=O)OC)C
SMILES (Isomeric) CC(C)C1CCC2(C3CCC4CCC=C4C2(C1NC3)CCC(=O)OC)C
InChI InChI=1S/C23H37NO2/c1-15(2)18-10-12-22(3)17-9-8-16-6-5-7-19(16)23(22,21(18)24-14-17)13-11-20(25)26-4/h7,15-18,21,24H,5-6,8-14H2,1-4H3
InChI Key WDKKUOYIQZUWGE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H37NO2
Molecular Weight 359.50 g/mol
Exact Mass 359.282429423 g/mol
Topological Polar Surface Area (TPSA) 38.30 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.72
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 3-(1-methyl-14-propan-2-yl-12-azatetracyclo[8.6.0.02,13.03,7]hexadec-3-en-2-yl)propanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.7855 78.55%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6502 65.02%
OATP2B1 inhibitior - 0.8660 86.60%
OATP1B1 inhibitior + 0.8667 86.67%
OATP1B3 inhibitior + 0.8934 89.34%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.5838 58.38%
P-glycoprotein inhibitior - 0.7363 73.63%
P-glycoprotein substrate + 0.5489 54.89%
CYP3A4 substrate + 0.6397 63.97%
CYP2C9 substrate - 0.8149 81.49%
CYP2D6 substrate - 0.7525 75.25%
CYP3A4 inhibition - 0.7296 72.96%
CYP2C9 inhibition + 0.5434 54.34%
CYP2C19 inhibition - 0.5477 54.77%
CYP2D6 inhibition - 0.8048 80.48%
CYP1A2 inhibition - 0.6529 65.29%
CYP2C8 inhibition - 0.5731 57.31%
CYP inhibitory promiscuity + 0.5122 51.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6277 62.77%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.9862 98.62%
Skin irritation - 0.7199 71.99%
Skin corrosion - 0.9198 91.98%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7773 77.73%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.5073 50.73%
skin sensitisation - 0.7585 75.85%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7836 78.36%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.8738 87.38%
Acute Oral Toxicity (c) III 0.6166 61.66%
Estrogen receptor binding + 0.7903 79.03%
Androgen receptor binding + 0.6979 69.79%
Thyroid receptor binding + 0.6002 60.02%
Glucocorticoid receptor binding + 0.8334 83.34%
Aromatase binding + 0.6829 68.29%
PPAR gamma - 0.6429 64.29%
Honey bee toxicity - 0.8564 85.64%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9562 95.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.15% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.90% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.23% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 96.86% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.88% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 91.39% 82.69%
CHEMBL2581 P07339 Cathepsin D 89.82% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.55% 97.25%
CHEMBL4227 P25090 Lipoxin A4 receptor 88.86% 100.00%
CHEMBL4208 P20618 Proteasome component C5 86.87% 90.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 86.36% 95.71%
CHEMBL3437 Q16853 Amine oxidase, copper containing 85.93% 94.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.89% 91.07%
CHEMBL4072 P07858 Cathepsin B 84.05% 93.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.58% 95.89%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 83.52% 91.03%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.42% 90.71%
CHEMBL221 P23219 Cyclooxygenase-1 83.28% 90.17%
CHEMBL5028 O14672 ADAM10 83.23% 97.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.99% 94.33%
CHEMBL1937 Q92769 Histone deacetylase 2 81.67% 94.75%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.02% 93.03%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.60% 96.77%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 80.13% 96.38%

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.
Daphniphyllum calycinum

Cross-Links

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PubChem 162915703
LOTUS LTS0215774
wikiData Q105302477