methyl (1R,2R,4S,5R,7R,11S,12S,15S,23R)-4,11-dihydroxy-18-methoxy-3-oxo-6-oxa-8,16-diazaoctacyclo[10.10.1.01,15.02,7.04,15.05,12.08,23.017,22]tricosa-17(22),18,20-triene-16-carboxylate

Details

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Internal ID 25befa3c-5ba9-4e8d-a5f1-1cc528987e06
Taxonomy Alkaloids and derivatives > Aspidofractine alkaloids
IUPAC Name methyl (1R,2R,4S,5R,7R,11S,12S,15S,23R)-4,11-dihydroxy-18-methoxy-3-oxo-6-oxa-8,16-diazaoctacyclo[10.10.1.01,15.02,7.04,15.05,12.08,23.017,22]tricosa-17(22),18,20-triene-16-carboxylate
SMILES (Canonical) COC1=CC=CC2=C1N(C34C25C6C7N8C5C(CC3)(C(CC8)O)C(C4(C6=O)O)O7)C(=O)OC
SMILES (Isomeric) COC1=CC=CC2=C1N([C@]34[C@]25[C@@H]6[C@@H]7N8[C@H]5[C@@](CC3)([C@H](CC8)O)[C@H]([C@@]4(C6=O)O)O7)C(=O)OC
InChI InChI=1S/C23H24N2O7/c1-30-11-5-3-4-10-14(11)25(19(28)31-2)21-8-7-20-12(26)6-9-24-16-13(22(10,21)17(20)24)15(27)23(21,29)18(20)32-16/h3-5,12-13,16-18,26,29H,6-9H2,1-2H3/t12-,13-,16+,17-,18+,20+,21-,22-,23+/m0/s1
InChI Key PHNDSUUWSBODRA-QXDQVDRTSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H24N2O7
Molecular Weight 440.40 g/mol
Exact Mass 440.15835111 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.16
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (1R,2R,4S,5R,7R,11S,12S,15S,23R)-4,11-dihydroxy-18-methoxy-3-oxo-6-oxa-8,16-diazaoctacyclo[10.10.1.01,15.02,7.04,15.05,12.08,23.017,22]tricosa-17(22),18,20-triene-16-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8527 85.27%
Caco-2 - 0.5718 57.18%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.5550 55.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9070 90.70%
OATP1B3 inhibitior + 0.9354 93.54%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8343 83.43%
P-glycoprotein inhibitior - 0.4480 44.80%
P-glycoprotein substrate + 0.6605 66.05%
CYP3A4 substrate + 0.7105 71.05%
CYP2C9 substrate - 0.8143 81.43%
CYP2D6 substrate - 0.6942 69.42%
CYP3A4 inhibition - 0.8196 81.96%
CYP2C9 inhibition - 0.7954 79.54%
CYP2C19 inhibition - 0.7412 74.12%
CYP2D6 inhibition - 0.8714 87.14%
CYP1A2 inhibition - 0.8634 86.34%
CYP2C8 inhibition + 0.4624 46.24%
CYP inhibitory promiscuity - 0.9170 91.70%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5688 56.88%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.9562 95.62%
Skin irritation - 0.8043 80.43%
Skin corrosion - 0.9421 94.21%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6093 60.93%
Micronuclear + 0.8400 84.00%
Hepatotoxicity - 0.5656 56.56%
skin sensitisation - 0.8768 87.68%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.6540 65.40%
Acute Oral Toxicity (c) III 0.6282 62.82%
Estrogen receptor binding + 0.8290 82.90%
Androgen receptor binding + 0.7475 74.75%
Thyroid receptor binding - 0.5490 54.90%
Glucocorticoid receptor binding + 0.6979 69.79%
Aromatase binding + 0.6886 68.86%
PPAR gamma + 0.6365 63.65%
Honey bee toxicity - 0.8666 86.66%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8984 89.84%

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 98.27% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.50% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.95% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.17% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.81% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 90.12% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.91% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.50% 94.45%
CHEMBL220 P22303 Acetylcholinesterase 89.36% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.91% 95.89%
CHEMBL4208 P20618 Proteasome component C5 86.74% 90.00%
CHEMBL5028 O14672 ADAM10 86.34% 97.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.95% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.48% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.42% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.21% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 81.70% 91.19%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.39% 90.71%

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 teoi

Cross-Links

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PubChem 44326312
LOTUS LTS0034849
wikiData Q105209111