(1S,2S,4S,7R,8S,11R)-6-acetyl-11-hydroxy-1',6'-dimethoxyspiro[10-oxa-5-azatricyclo[5.3.1.04,8]undec-5-ene-2,3'-indole]-2'-one

Details

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Internal ID b609c898-f691-4cfd-8925-97bc5ad4cb05
Taxonomy Organoheterocyclic compounds > Indoles and derivatives
IUPAC Name (1S,2S,4S,7R,8S,11R)-6-acetyl-11-hydroxy-1',6'-dimethoxyspiro[10-oxa-5-azatricyclo[5.3.1.04,8]undec-5-ene-2,3'-indole]-2'-one
SMILES (Canonical) CC(=O)C1=NC2CC3(C4C(C1C2CO4)O)C5=C(C=C(C=C5)OC)N(C3=O)OC
SMILES (Isomeric) CC(=O)C1=N[C@H]2C[C@@]3([C@H]4[C@@H]([C@@H]1[C@@H]2CO4)O)C5=C(C=C(C=C5)OC)N(C3=O)OC
InChI InChI=1S/C20H22N2O6/c1-9(23)16-15-11-8-28-18(17(15)24)20(7-13(11)21-16)12-5-4-10(26-2)6-14(12)22(27-3)19(20)25/h4-6,11,13,15,17-18,24H,7-8H2,1-3H3/t11-,13+,15-,17-,18-,20+/m1/s1
InChI Key XTCNHYCPNSGXRX-PXUXMEPPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H22N2O6
Molecular Weight 386.40 g/mol
Exact Mass 386.14778643 g/mol
Topological Polar Surface Area (TPSA) 97.70 Ų
XlogP -0.70
Atomic LogP (AlogP) 0.65
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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XTCNHYCPNSGXRX-PXUXMEPPSA-N

2D Structure

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2D Structure of (1S,2S,4S,7R,8S,11R)-6-acetyl-11-hydroxy-1',6'-dimethoxyspiro[10-oxa-5-azatricyclo[5.3.1.04,8]undec-5-ene-2,3'-indole]-2'-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8996 89.96%
Caco-2 + 0.5631 56.31%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.5949 59.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9155 91.55%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4801 48.01%
P-glycoprotein inhibitior - 0.5627 56.27%
P-glycoprotein substrate + 0.5116 51.16%
CYP3A4 substrate + 0.6748 67.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8217 82.17%
CYP3A4 inhibition + 0.5063 50.63%
CYP2C9 inhibition - 0.5811 58.11%
CYP2C19 inhibition - 0.5911 59.11%
CYP2D6 inhibition - 0.8770 87.70%
CYP1A2 inhibition - 0.7566 75.66%
CYP2C8 inhibition - 0.5935 59.35%
CYP inhibitory promiscuity - 0.7518 75.18%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5578 55.78%
Eye corrosion - 0.9817 98.17%
Eye irritation - 0.9625 96.25%
Skin irritation - 0.7808 78.08%
Skin corrosion - 0.9319 93.19%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.6057 60.57%
skin sensitisation - 0.8427 84.27%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.5948 59.48%
Acute Oral Toxicity (c) III 0.6187 61.87%
Estrogen receptor binding + 0.8415 84.15%
Androgen receptor binding + 0.6730 67.30%
Thyroid receptor binding + 0.6453 64.53%
Glucocorticoid receptor binding + 0.6264 62.64%
Aromatase binding - 0.5060 50.60%
PPAR gamma + 0.6072 60.72%
Honey bee toxicity - 0.7646 76.46%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9200 92.00%

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 98.91% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.04% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.19% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.42% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.15% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.74% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.56% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.44% 93.40%
CHEMBL226 P30542 Adenosine A1 receptor 87.60% 95.93%
CHEMBL3137261 O14744 PRMT5/MEP50 complex 87.34% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.15% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.68% 94.45%
CHEMBL2535 P11166 Glucose transporter 85.34% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.73% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.71% 90.71%
CHEMBL4208 P20618 Proteasome component C5 83.42% 90.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.93% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.73% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.44% 92.62%
CHEMBL340 P08684 Cytochrome P450 3A4 80.97% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.04% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.01% 91.07%

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.
Gelsemium sempervirens

Cross-Links

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PubChem 12070887
LOTUS LTS0012463
wikiData Q105341458