11-Ethyl-13-(hydroxymethyl)-4,16,18-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol

Details

Top
Internal ID 976a7295-45e4-4a96-9c03-6747357a7d21
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Aconitane-type diterpenoid alkaloids
IUPAC Name 11-ethyl-13-(hydroxymethyl)-4,16,18-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol
SMILES (Canonical) CCN1CC2(CCC(C34C2C(C(C31)(C5(CCC6CC4C5C6OC)O)O)OC)OC)CO
SMILES (Isomeric) CCN1CC2(CCC(C34C2C(C(C31)(C5(CCC6CC4C5C6OC)O)O)OC)OC)CO
InChI InChI=1S/C24H39NO6/c1-5-25-11-21(12-26)8-7-15(29-2)23-14-10-13-6-9-22(27,16(14)17(13)30-3)24(28,20(23)25)19(31-4)18(21)23/h13-20,26-28H,5-12H2,1-4H3
InChI Key SRLOJAMIILIMMJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H39NO6
Molecular Weight 437.60 g/mol
Exact Mass 437.27773796 g/mol
Topological Polar Surface Area (TPSA) 91.60 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.65
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 11-Ethyl-13-(hydroxymethyl)-4,16,18-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6595 65.95%
Caco-2 - 0.6307 63.07%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.6712 67.12%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9021 90.21%
OATP1B3 inhibitior + 0.9415 94.15%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.5225 52.25%
P-glycoprotein inhibitior - 0.8893 88.93%
P-glycoprotein substrate + 0.5899 58.99%
CYP3A4 substrate + 0.6721 67.21%
CYP2C9 substrate - 0.8114 81.14%
CYP2D6 substrate + 0.3571 35.71%
CYP3A4 inhibition - 0.8647 86.47%
CYP2C9 inhibition - 0.8943 89.43%
CYP2C19 inhibition - 0.9088 90.88%
CYP2D6 inhibition - 0.9213 92.13%
CYP1A2 inhibition - 0.9285 92.85%
CYP2C8 inhibition + 0.5247 52.47%
CYP inhibitory promiscuity - 0.9741 97.41%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6286 62.86%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.9343 93.43%
Skin irritation - 0.7688 76.88%
Skin corrosion - 0.9300 93.00%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7409 74.09%
Micronuclear + 0.5800 58.00%
Hepatotoxicity - 0.6442 64.42%
skin sensitisation - 0.8598 85.98%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.7674 76.74%
Acute Oral Toxicity (c) III 0.4928 49.28%
Estrogen receptor binding + 0.7527 75.27%
Androgen receptor binding + 0.7410 74.10%
Thyroid receptor binding + 0.6956 69.56%
Glucocorticoid receptor binding - 0.4642 46.42%
Aromatase binding + 0.6659 66.59%
PPAR gamma + 0.6668 66.68%
Honey bee toxicity - 0.7914 79.14%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.8508 85.08%

Targets

Top

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 98.75% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.24% 96.09%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 94.39% 95.58%
CHEMBL4040 P28482 MAP kinase ERK2 93.67% 83.82%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.13% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.70% 94.45%
CHEMBL226 P30542 Adenosine A1 receptor 86.72% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.79% 95.89%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.51% 96.61%
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 85.25% 92.38%
CHEMBL2996 Q05655 Protein kinase C delta 85.05% 97.79%
CHEMBL2534 O15530 3-phosphoinositide dependent protein kinase-1 83.91% 95.36%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 83.80% 91.03%
CHEMBL3820 P35557 Hexokinase type IV 83.29% 91.96%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.33% 97.28%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.98% 92.62%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.52% 92.94%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 81.44% 100.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.80% 93.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.57% 89.62%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.32% 97.50%
CHEMBL1991 O14920 Inhibitor of nuclear factor kappa B kinase beta subunit 80.11% 97.15%

Plants that contains it

Top
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 cuneatum

Cross-Links

Top
PubChem 162871191
LOTUS LTS0136608
wikiData Q105259269