14-Ethyl-6-methoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19,21-triol

Details

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Internal ID 0aa1459f-1b52-445c-ba83-07c1cbcc6341
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Aconitane-type diterpenoid alkaloids
IUPAC Name 14-ethyl-6-methoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19,21-triol
SMILES (Canonical) CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7O)OC)OCO5)O)O)C
SMILES (Isomeric) CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7O)OC)OCO5)O)O)C
InChI InChI=1S/C23H35NO6/c1-4-24-9-20(2)6-5-14(25)22-12-7-11-13(28-3)8-21(15(12)16(11)26)23(19(22)24,30-10-29-21)18(27)17(20)22/h11-19,25-27H,4-10H2,1-3H3
InChI Key ZHIUGHDKWOISDE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H35NO6
Molecular Weight 421.50 g/mol
Exact Mass 421.24643784 g/mol
Topological Polar Surface Area (TPSA) 91.60 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.36
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 14-Ethyl-6-methoxy-16-methyl-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19,21-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6828 68.28%
Caco-2 - 0.5825 58.25%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.6960 69.60%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9123 91.23%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6128 61.28%
P-glycoprotein inhibitior - 0.8914 89.14%
P-glycoprotein substrate + 0.5895 58.95%
CYP3A4 substrate + 0.6975 69.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3849 38.49%
CYP3A4 inhibition - 0.9020 90.20%
CYP2C9 inhibition - 0.9087 90.87%
CYP2C19 inhibition - 0.8949 89.49%
CYP2D6 inhibition - 0.9354 93.54%
CYP1A2 inhibition - 0.9296 92.96%
CYP2C8 inhibition + 0.6073 60.73%
CYP inhibitory promiscuity - 0.9358 93.58%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5492 54.92%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.8986 89.86%
Skin irritation - 0.7934 79.34%
Skin corrosion - 0.9371 93.71%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6615 66.15%
Micronuclear + 0.5200 52.00%
Hepatotoxicity - 0.6070 60.70%
skin sensitisation - 0.8615 86.15%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.6490 64.90%
Acute Oral Toxicity (c) III 0.4324 43.24%
Estrogen receptor binding + 0.6725 67.25%
Androgen receptor binding + 0.7447 74.47%
Thyroid receptor binding + 0.7382 73.82%
Glucocorticoid receptor binding + 0.5374 53.74%
Aromatase binding + 0.6869 68.69%
PPAR gamma + 0.6104 61.04%
Honey bee toxicity - 0.7195 71.95%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.5959 59.59%

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 98.58% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.56% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.91% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.35% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.95% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.94% 91.11%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.46% 95.17%
CHEMBL221 P23219 Cyclooxygenase-1 88.37% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.06% 100.00%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 88.05% 95.58%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.78% 92.62%
CHEMBL2581 P07339 Cathepsin D 87.07% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.65% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.70% 95.89%
CHEMBL1871 P10275 Androgen Receptor 84.95% 96.43%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.10% 96.77%
CHEMBL226 P30542 Adenosine A1 receptor 84.03% 95.93%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.75% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.03% 94.00%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.69% 95.50%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.00% 82.69%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.10% 97.28%

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.
Delphinium anthriscifolium
Delphinium yunnanense

Cross-Links

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PubChem 73657141
LOTUS LTS0046719
wikiData Q105375774