[5,9,16-trihydroxy-6,18,20-trimethoxy-15-(methoxymethyl)-10,13-dimethyl-13-azahexacyclo[9.7.2.12,5.01,12.03,10.015,19]henicosan-4-yl] benzoate

Details

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Internal ID b9743656-9c5b-47b9-8689-51498b5a183f
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name [5,9,16-trihydroxy-6,18,20-trimethoxy-15-(methoxymethyl)-10,13-dimethyl-13-azahexacyclo[9.7.2.12,5.01,12.03,10.015,19]henicosan-4-yl] benzoate
SMILES (Canonical) CC12C(CCC(C3(CC(C1C3OC(=O)C4=CC=CC=C4)C56C(CC(C7(C5C(C2C6N(C7)C)OC)COC)O)OC)O)OC)O
SMILES (Isomeric) CC12C(CCC(C3(CC(C1C3OC(=O)C4=CC=CC=C4)C56C(CC(C7(C5C(C2C6N(C7)C)OC)COC)O)OC)O)OC)O
InChI InChI=1S/C34H49NO9/c1-31-20(36)12-13-22(41-4)33(39)15-19(24(31)29(33)44-30(38)18-10-8-7-9-11-18)34-23(42-5)14-21(37)32(17-40-3)16-35(2)28(34)25(31)26(43-6)27(32)34/h7-11,19-29,36-37,39H,12-17H2,1-6H3
InChI Key CLNODDZVJJQWNZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H49NO9
Molecular Weight 615.80 g/mol
Exact Mass 615.34073214 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.74
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [5,9,16-trihydroxy-6,18,20-trimethoxy-15-(methoxymethyl)-10,13-dimethyl-13-azahexacyclo[9.7.2.12,5.01,12.03,10.015,19]henicosan-4-yl] benzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7303 73.03%
Caco-2 - 0.7851 78.51%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.4488 44.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9164 91.64%
OATP1B3 inhibitior + 0.9363 93.63%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7349 73.49%
BSEP inhibitior + 0.9213 92.13%
P-glycoprotein inhibitior + 0.6230 62.30%
P-glycoprotein substrate + 0.7297 72.97%
CYP3A4 substrate + 0.7425 74.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6848 68.48%
CYP3A4 inhibition - 0.7108 71.08%
CYP2C9 inhibition - 0.9107 91.07%
CYP2C19 inhibition - 0.9013 90.13%
CYP2D6 inhibition - 0.9193 91.93%
CYP1A2 inhibition - 0.9311 93.11%
CYP2C8 inhibition + 0.7391 73.91%
CYP inhibitory promiscuity - 0.9610 96.10%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5842 58.42%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.9229 92.29%
Skin irritation - 0.7754 77.54%
Skin corrosion - 0.9492 94.92%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7383 73.83%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.8862 88.62%
Respiratory toxicity + 0.9444 94.44%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity - 0.8956 89.56%
Acute Oral Toxicity (c) I 0.4349 43.49%
Estrogen receptor binding + 0.8071 80.71%
Androgen receptor binding + 0.6490 64.90%
Thyroid receptor binding + 0.5791 57.91%
Glucocorticoid receptor binding - 0.6061 60.61%
Aromatase binding + 0.7309 73.09%
PPAR gamma + 0.7314 73.14%
Honey bee toxicity - 0.8279 82.79%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5245 52.45%
Fish aquatic toxicity + 0.7512 75.12%

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 99.55% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.32% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.77% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 92.64% 90.17%
CHEMBL4040 P28482 MAP kinase ERK2 90.29% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.27% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.85% 85.14%
CHEMBL4208 P20618 Proteasome component C5 89.65% 90.00%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 87.61% 91.43%
CHEMBL5028 O14672 ADAM10 86.34% 97.50%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.31% 91.07%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.01% 99.23%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.22% 96.00%
CHEMBL2096618 P11274 Bcr/Abl fusion protein 84.92% 85.83%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.65% 95.89%
CHEMBL1741221 Q9Y4P1 Cysteine protease ATG4B 83.60% 87.50%
CHEMBL340 P08684 Cytochrome P450 3A4 83.03% 91.19%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.42% 93.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.39% 97.14%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.23% 100.00%
CHEMBL2535 P11166 Glucose transporter 80.82% 98.75%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.40% 94.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.13% 97.25%

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.
Aconitum carmichaelii
Aconitum kusnezoffii
Aconitum napellus

Cross-Links

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PubChem 53399190
NPASS NPC206888