Oxostephanine

Details

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Internal ID 0cb6e6e2-039d-4ebd-a017-8979f3bb1516
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 15-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,9,11,14(19),15,17-octaen-13-one
SMILES (Canonical) COC1=CC=CC2=C1C(=O)C3=NC=CC4=CC5=C(C2=C43)OCO5
SMILES (Isomeric) COC1=CC=CC2=C1C(=O)C3=NC=CC4=CC5=C(C2=C43)OCO5
InChI InChI=1S/C18H11NO4/c1-21-11-4-2-3-10-14(11)17(20)16-13-9(5-6-19-16)7-12-18(15(10)13)23-8-22-12/h2-7H,8H2,1H3
InChI Key HPWGRUBQQWPQKG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H11NO4
Molecular Weight 305.30 g/mol
Exact Mass 305.06880783 g/mol
Topological Polar Surface Area (TPSA) 57.60 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.18
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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NSC383228
CHEMBL521933
NSC-383228
58262-58-1

2D Structure

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2D Structure of Oxostephanine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9928 99.28%
Caco-2 + 0.7733 77.33%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6085 60.85%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9512 95.12%
OATP1B3 inhibitior + 0.9681 96.81%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8229 82.29%
P-glycoprotein inhibitior - 0.6170 61.70%
P-glycoprotein substrate - 0.7556 75.56%
CYP3A4 substrate + 0.5998 59.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7999 79.99%
CYP3A4 inhibition + 0.9177 91.77%
CYP2C9 inhibition - 0.5242 52.42%
CYP2C19 inhibition + 0.8236 82.36%
CYP2D6 inhibition - 0.5256 52.56%
CYP1A2 inhibition + 0.9424 94.24%
CYP2C8 inhibition + 0.5905 59.05%
CYP inhibitory promiscuity + 0.9189 91.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5169 51.69%
Eye corrosion - 0.9804 98.04%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.7873 78.73%
Skin corrosion - 0.9649 96.49%
Ames mutagenesis + 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4186 41.86%
Micronuclear + 0.7474 74.74%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.7872 78.72%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.8585 85.85%
Acute Oral Toxicity (c) III 0.7343 73.43%
Estrogen receptor binding + 0.8900 89.00%
Androgen receptor binding + 0.6093 60.93%
Thyroid receptor binding + 0.6601 66.01%
Glucocorticoid receptor binding + 0.9011 90.11%
Aromatase binding + 0.7158 71.58%
PPAR gamma + 0.8137 81.37%
Honey bee toxicity - 0.7991 79.91%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.5374 53.74%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.06% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.54% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.29% 96.77%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 94.70% 96.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 94.60% 94.03%
CHEMBL2581 P07339 Cathepsin D 94.28% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.86% 89.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 93.13% 96.67%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 92.79% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.29% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.88% 96.09%
CHEMBL2535 P11166 Glucose transporter 91.34% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.38% 96.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.06% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.73% 95.56%
CHEMBL5747 Q92793 CREB-binding protein 89.59% 95.12%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 88.10% 82.67%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.00% 94.80%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 87.11% 95.71%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 86.89% 92.38%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 86.71% 96.39%
CHEMBL5014 O43353 Serine/threonine-protein kinase RIPK2 86.23% 86.79%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.68% 91.11%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.93% 92.62%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.31% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.82% 94.75%
CHEMBL3401 O75469 Pregnane X receptor 83.47% 94.73%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 83.12% 80.96%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.83% 93.10%
CHEMBL2047 Q96RI1 Bile acid receptor FXR 82.53% 96.10%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.25% 94.42%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 82.18% 100.00%
CHEMBL3116 P50750 Cyclin-dependent kinase 9 82.03% 96.31%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.19% 99.18%
CHEMBL1907599 P05556 Integrin alpha-4/beta-1 80.65% 92.86%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.21% 95.17%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.07% 85.30%

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.
Goniothalamus scortechinii
Greenwayodendron suaveolens
Guatteria maypurensis
Orobanche coerulescens
Polyalthia insignis
Polyalthia stenopetala
Stephania japonica
Stephania venosa
Trivalvaria macrophylla

Cross-Links

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PubChem 343547
NPASS NPC166722
LOTUS LTS0048190
wikiData Q104253123