[(1R,2S,3S,4S,5S,7R,8S,9R,11R,12S,13R,14R,16S,17R,18S)-4,18-diacetyloxy-13-benzoyloxy-7-formyl-16,17-dihydroxy-7,10-dimethyl-15-methylidene-10-azahexacyclo[7.7.1.12,14.01,12.03,8.03,11]octadecan-5-yl] benzoate

Details

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Internal ID 60be6b2f-321b-4049-910d-f40c222c854f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Villanovane, atisane, trachylobane or helvifulvane diterpenoids > Atisane diterpenoids
IUPAC Name [(1R,2S,3S,4S,5S,7R,8S,9R,11R,12S,13R,14R,16S,17R,18S)-4,18-diacetyloxy-13-benzoyloxy-7-formyl-16,17-dihydroxy-7,10-dimethyl-15-methylidene-10-azahexacyclo[7.7.1.12,14.01,12.03,8.03,11]octadecan-5-yl] benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C39H41NO11/c1-18-24-27(51-36(47)22-14-10-7-11-15-22)25-31-39-29(26(40(31)5)33(45)38(25,32(18)44)30(39)28(24)48-19(2)42)37(4,17-41)16-23(34(39)49-20(3)43)50-35(46)21-12-8-6-9-13-21/h6-15,17,23-34,44-45H,1,16H2,2-5H3/t23-,24-,25+,26+,27-,28+,29+,30+,31+,32-,33-,34+,37-,38-,39-/m0/s1
InChI Key SKPOUZKDPRGKHR-JXJUCQPOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C39H41NO11
Molecular Weight 699.70 g/mol
Exact Mass 699.26796112 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 12
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1R,2S,3S,4S,5S,7R,8S,9R,11R,12S,13R,14R,16S,17R,18S)-4,18-diacetyloxy-13-benzoyloxy-7-formyl-16,17-dihydroxy-7,10-dimethyl-15-methylidene-10-azahexacyclo[7.7.1.12,14.01,12.03,8.03,11]octadecan-5-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 + 0.7690 76.90%
Caco-2 - 0.8350 83.50%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.3695 36.95%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.8678 86.78%
OATP1B3 inhibitior + 0.9270 92.70%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9546 95.46%
P-glycoprotein inhibitior + 0.7954 79.54%
P-glycoprotein substrate + 0.6350 63.50%
CYP3A4 substrate + 0.6899 68.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7305 73.05%
CYP3A4 inhibition - 0.8053 80.53%
CYP2C9 inhibition - 0.8241 82.41%
CYP2C19 inhibition - 0.7280 72.80%
CYP2D6 inhibition - 0.8902 89.02%
CYP1A2 inhibition - 0.8065 80.65%
CYP2C8 inhibition + 0.6016 60.16%
CYP inhibitory promiscuity - 0.7920 79.20%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.3926 39.26%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.9003 90.03%
Skin irritation - 0.7838 78.38%
Skin corrosion - 0.9326 93.26%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7194 71.94%
Micronuclear + 0.6600 66.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8454 84.54%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.5274 52.74%
Acute Oral Toxicity (c) III 0.5198 51.98%
Estrogen receptor binding + 0.7495 74.95%
Androgen receptor binding + 0.7000 70.00%
Thyroid receptor binding + 0.6100 61.00%
Glucocorticoid receptor binding + 0.6630 66.30%
Aromatase binding + 0.5478 54.78%
PPAR gamma + 0.7236 72.36%
Honey bee toxicity - 0.7568 75.68%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5355 53.55%
Fish aquatic toxicity + 0.9502 95.02%

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
CHEMBL240 Q12809 HERG 98.89% 89.76%
CHEMBL221 P23219 Cyclooxygenase-1 98.19% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.34% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.58% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.51% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.34% 86.33%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 90.06% 94.08%
CHEMBL4208 P20618 Proteasome component C5 87.74% 90.00%
CHEMBL340 P08684 Cytochrome P450 3A4 86.89% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.69% 95.89%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 85.77% 83.00%
CHEMBL5028 O14672 ADAM10 84.97% 97.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.22% 94.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.21% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.06% 95.50%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.24% 82.69%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.12% 96.47%

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 trifoliolatum

Cross-Links

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PubChem 163105977
LOTUS LTS0187615
wikiData Q105254978