methyl (2R,5R,6S,8S,9S,10R)-14-[(1R,9S,12R,13Z,18R)-13-ethylidene-4-methoxy-18-methoxycarbonyl-6-methyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-trien-5-yl]-15-methoxy-6,18-dimethyl-3-(2-methylpropanoyl)-7-oxa-3,18-diazapentacyclo[9.7.0.02,8.05,9.012,17]octadeca-1(11),12,14,16-tetraene-10-carboxylate

Details

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Internal ID e58dfda5-60ad-45b1-b898-c1cbe964f532
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name methyl (2R,5R,6S,8S,9S,10R)-14-[(1R,9S,12R,13Z,18R)-13-ethylidene-4-methoxy-18-methoxycarbonyl-6-methyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-trien-5-yl]-15-methoxy-6,18-dimethyl-3-(2-methylpropanoyl)-7-oxa-3,18-diazapentacyclo[9.7.0.02,8.05,9.012,17]octadeca-1(11),12,14,16-tetraene-10-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C46H56N4O8/c1-11-24-19-49-15-14-45-29-17-32(55-8)33(22(4)38(29)47-46(45,49)13-12-25(24)37(45)44(53)57-10)27-16-26-30(18-31(27)54-7)48(6)39-34(26)36(43(52)56-9)35-28-20-50(42(51)21(2)3)40(39)41(35)58-23(28)5/h11,16-18,21,23,25,28,35-37,40-41,47H,12-15,19-20H2,1-10H3/b24-11+/t23-,25-,28+,35-,36-,37-,40+,41-,45-,46-/m0/s1
InChI Key OZBMAEUURAGYOB-NUPMTUBOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C46H56N4O8
Molecular Weight 793.00 g/mol
Exact Mass 792.40981476 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 6.22
H-Bond Acceptor 11
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (2R,5R,6S,8S,9S,10R)-14-[(1R,9S,12R,13Z,18R)-13-ethylidene-4-methoxy-18-methoxycarbonyl-6-methyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-trien-5-yl]-15-methoxy-6,18-dimethyl-3-(2-methylpropanoyl)-7-oxa-3,18-diazapentacyclo[9.7.0.02,8.05,9.012,17]octadeca-1(11),12,14,16-tetraene-10-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9774 97.74%
Caco-2 - 0.8323 83.23%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.4793 47.93%
OATP2B1 inhibitior - 0.5631 56.31%
OATP1B1 inhibitior + 0.8170 81.70%
OATP1B3 inhibitior + 0.9237 92.37%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.9882 98.82%
P-glycoprotein inhibitior + 0.8259 82.59%
P-glycoprotein substrate + 0.8369 83.69%
CYP3A4 substrate + 0.7467 74.67%
CYP2C9 substrate - 0.5955 59.55%
CYP2D6 substrate - 0.8418 84.18%
CYP3A4 inhibition + 0.5735 57.35%
CYP2C9 inhibition - 0.5780 57.80%
CYP2C19 inhibition - 0.5407 54.07%
CYP2D6 inhibition - 0.7929 79.29%
CYP1A2 inhibition + 0.5418 54.18%
CYP2C8 inhibition + 0.7839 78.39%
CYP inhibitory promiscuity - 0.5513 55.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6166 61.66%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.9137 91.37%
Skin irritation - 0.7749 77.49%
Skin corrosion - 0.9327 93.27%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7180 71.80%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.5146 51.46%
skin sensitisation - 0.8625 86.25%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.7980 79.80%
Acute Oral Toxicity (c) III 0.6174 61.74%
Estrogen receptor binding + 0.8484 84.84%
Androgen receptor binding + 0.7813 78.13%
Thyroid receptor binding + 0.6251 62.51%
Glucocorticoid receptor binding + 0.8326 83.26%
Aromatase binding + 0.7188 71.88%
PPAR gamma + 0.7861 78.61%
Honey bee toxicity - 0.6642 66.42%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9851 98.51%

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 97.72% 96.09%
CHEMBL284 P27487 Dipeptidyl peptidase IV 97.52% 95.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.36% 95.56%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 95.79% 96.38%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 94.02% 89.62%
CHEMBL2581 P07339 Cathepsin D 93.64% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.86% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.35% 89.00%
CHEMBL255 P29275 Adenosine A2b receptor 92.25% 98.59%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 92.21% 95.34%
CHEMBL1914 P06276 Butyrylcholinesterase 92.01% 95.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.92% 97.21%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 91.15% 93.03%
CHEMBL5747 Q92793 CREB-binding protein 90.86% 95.12%
CHEMBL1937 Q92769 Histone deacetylase 2 89.05% 94.75%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 89.01% 89.05%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.95% 91.11%
CHEMBL3922 P50579 Methionine aminopeptidase 2 88.55% 97.28%
CHEMBL340 P08684 Cytochrome P450 3A4 88.48% 91.19%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.04% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.10% 86.33%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 86.61% 97.31%
CHEMBL2413 P32246 C-C chemokine receptor type 1 86.55% 89.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.30% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.10% 94.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 85.88% 82.38%
CHEMBL5028 O14672 ADAM10 85.62% 97.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.92% 95.89%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.31% 94.80%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.29% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.91% 96.21%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.34% 100.00%
CHEMBL2535 P11166 Glucose transporter 83.14% 98.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.94% 85.14%
CHEMBL4208 P20618 Proteasome component C5 82.34% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.14% 96.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.61% 100.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.16% 91.03%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.00% 93.00%

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.
Catharanthus roseus

Cross-Links

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PubChem 100933831
NPASS NPC48028
LOTUS LTS0257068
wikiData Q105203655