Oxo-O-methylbulbocapnine

Details

Top
Internal ID f147bc54-fced-4867-9f77-3e971a71e176
Taxonomy Alkaloids and derivatives > Aporphines
IUPAC Name 17,18-dimethoxy-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)
SMILES (Isomeric)
InChI InChI=1S/C19H13NO5/c1-22-11-4-3-10-14(18(11)23-2)15-13-9(5-6-20-16(13)17(10)21)7-12-19(15)25-8-24-12/h3-7H,8H2,1-2H3
InChI Key JHVUBEPVDZDPDJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H13NO5
Molecular Weight 335.30 g/mol
Exact Mass 335.07937252 g/mol
Topological Polar Surface Area (TPSA) 66.90 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

Top
NSC617672
NSC-617672
17,18-dimethoxy-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

2D Structure

Top
2D Structure of Oxo-O-methylbulbocapnine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9872 98.72%
Caco-2 + 0.8789 87.89%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6170 61.70%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.9507 95.07%
OATP1B3 inhibitior + 0.9520 95.20%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8014 80.14%
P-glycoprotein inhibitior - 0.5717 57.17%
P-glycoprotein substrate - 0.7438 74.38%
CYP3A4 substrate + 0.5919 59.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7812 78.12%
CYP3A4 inhibition + 0.9390 93.90%
CYP2C9 inhibition + 0.5574 55.74%
CYP2C19 inhibition + 0.8585 85.85%
CYP2D6 inhibition - 0.5112 51.12%
CYP1A2 inhibition + 0.9356 93.56%
CYP2C8 inhibition + 0.5704 57.04%
CYP inhibitory promiscuity + 0.9451 94.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5466 54.66%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.4783 47.83%
Skin irritation - 0.7973 79.73%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis + 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4182 41.82%
Micronuclear + 0.7174 71.74%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8131 81.31%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6530 65.30%
Acute Oral Toxicity (c) III 0.6735 67.35%
Estrogen receptor binding + 0.8746 87.46%
Androgen receptor binding + 0.5596 55.96%
Thyroid receptor binding + 0.7151 71.51%
Glucocorticoid receptor binding + 0.9258 92.58%
Aromatase binding + 0.6629 66.29%
PPAR gamma + 0.8423 84.23%
Honey bee toxicity - 0.7941 79.41%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.6612 66.12%

Targets

Top

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 97.47% 94.00%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 96.05% 96.09%
CHEMBL5747 Q92793 CREB-binding protein 95.52% 95.12%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.24% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.76% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 94.09% 96.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.90% 89.00%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 93.59% 82.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.44% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.67% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 89.51% 91.49%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 87.75% 96.00%
CHEMBL2581 P07339 Cathepsin D 87.72% 98.95%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.65% 94.42%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.45% 99.23%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 86.62% 95.78%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 86.45% 94.03%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 86.02% 92.38%
CHEMBL2535 P11166 Glucose transporter 85.25% 98.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.43% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 83.81% 94.75%
CHEMBL4302 P08183 P-glycoprotein 1 83.60% 92.98%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 83.49% 93.10%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.43% 85.14%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 83.33% 85.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.96% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.88% 95.56%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 82.65% 80.96%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.60% 92.62%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.16% 94.80%
CHEMBL3401 O75469 Pregnane X receptor 81.63% 94.73%
CHEMBL6175 Q9H3R0 Lysine-specific demethylase 4C 80.80% 96.69%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.53% 82.38%

Plants that contains it

Top
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.
Hernandia nymphaeifolia

Cross-Links

Top
PubChem 357992
LOTUS LTS0097855
wikiData Q105128393