dimethyl (1R,9S,16R,19R,20S)-4-methoxy-21-oxo-2,12-diazahexacyclo[10.6.2.19,16.01,9.03,8.016,20]henicosa-3(8),4,6-triene-2,19-dicarboxylate

Details

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Internal ID a9bd7979-8b6d-41ec-8b51-90d234883b3a
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name dimethyl (1R,9S,16R,19R,20S)-4-methoxy-21-oxo-2,12-diazahexacyclo[10.6.2.19,16.01,9.03,8.016,20]henicosa-3(8),4,6-triene-2,19-dicarboxylate
SMILES (Canonical) COC1=CC=CC2=C1N(C34C25CCN6CCCC(C6C3C(=O)OC)(C5=O)CC4)C(=O)OC
SMILES (Isomeric) COC1=CC=CC2=C1N([C@@]34[C@]25CCN6CCC[C@@]([C@@H]6[C@H]3C(=O)OC)(C5=O)CC4)C(=O)OC
InChI InChI=1S/C24H28N2O6/c1-30-15-7-4-6-14-17(15)26(21(29)32-3)24-10-9-22-8-5-12-25(13-11-23(14,24)20(22)28)18(22)16(24)19(27)31-2/h4,6-7,16,18H,5,8-13H2,1-3H3/t16-,18-,22+,23+,24+/m0/s1
InChI Key YNEYAFZLABTIDN-XFNUAGFQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H28N2O6
Molecular Weight 440.50 g/mol
Exact Mass 440.19473662 g/mol
Topological Polar Surface Area (TPSA) 85.40 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of dimethyl (1R,9S,16R,19R,20S)-4-methoxy-21-oxo-2,12-diazahexacyclo[10.6.2.19,16.01,9.03,8.016,20]henicosa-3(8),4,6-triene-2,19-dicarboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9238 92.38%
Caco-2 + 0.6569 65.69%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.5896 58.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9007 90.07%
OATP1B3 inhibitior + 0.9380 93.80%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8735 87.35%
P-glycoprotein inhibitior + 0.7344 73.44%
P-glycoprotein substrate + 0.5412 54.12%
CYP3A4 substrate + 0.6927 69.27%
CYP2C9 substrate - 0.7987 79.87%
CYP2D6 substrate + 0.4260 42.60%
CYP3A4 inhibition + 0.5471 54.71%
CYP2C9 inhibition - 0.8571 85.71%
CYP2C19 inhibition - 0.6940 69.40%
CYP2D6 inhibition - 0.8210 82.10%
CYP1A2 inhibition - 0.7500 75.00%
CYP2C8 inhibition - 0.6304 63.04%
CYP inhibitory promiscuity - 0.6618 66.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6357 63.57%
Eye corrosion - 0.9870 98.70%
Eye irritation - 0.9645 96.45%
Skin irritation - 0.8267 82.67%
Skin corrosion - 0.9515 95.15%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6689 66.89%
Micronuclear + 0.7100 71.00%
Hepatotoxicity - 0.5573 55.73%
skin sensitisation - 0.8858 88.58%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.5707 57.07%
Acute Oral Toxicity (c) III 0.6190 61.90%
Estrogen receptor binding + 0.7052 70.52%
Androgen receptor binding + 0.7708 77.08%
Thyroid receptor binding - 0.5193 51.93%
Glucocorticoid receptor binding + 0.6435 64.35%
Aromatase binding + 0.5620 56.20%
PPAR gamma + 0.5535 55.35%
Honey bee toxicity - 0.7577 75.77%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9454 94.54%

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 96.99% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.70% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 93.24% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.41% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.10% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.02% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.36% 94.45%
CHEMBL2535 P11166 Glucose transporter 88.83% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.70% 99.23%
CHEMBL5028 O14672 ADAM10 87.58% 97.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.98% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.46% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.19% 91.11%
CHEMBL220 P22303 Acetylcholinesterase 85.85% 94.45%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.15% 93.03%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.91% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.68% 91.19%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.79% 90.71%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.61% 97.14%
CHEMBL4208 P20618 Proteasome component C5 80.33% 90.00%

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.
Kopsia griffithii
Kopsia pauciflora

Cross-Links

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PubChem 163106747
LOTUS LTS0235080
wikiData Q105350907