Benzo(g)-1,3-benzodioxolo(5,6-a)quinolizinium, 5,6-dihydro-9,10-dimethoxy-13-methyl-

Details

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Internal ID 057456f5-0d3f-4975-85a1-92ab1d9de278
Taxonomy Alkaloids and derivatives > Protoberberine alkaloids and derivatives
IUPAC Name 16,17-dimethoxy-21-methyl-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaene
SMILES (Canonical) CC1=C2C=CC(=C(C2=C[N+]3=C1C4=CC5=C(C=C4CC3)OCO5)OC)OC
SMILES (Isomeric) CC1=C2C=CC(=C(C2=C[N+]3=C1C4=CC5=C(C=C4CC3)OCO5)OC)OC
InChI InChI=1S/C21H20NO4/c1-12-14-4-5-17(23-2)21(24-3)16(14)10-22-7-6-13-8-18-19(26-11-25-18)9-15(13)20(12)22/h4-5,8-10H,6-7,11H2,1-3H3/q+1
InChI Key SMERZMDSMLIVHC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20NO4+
Molecular Weight 350.40 g/mol
Exact Mass 350.13923312 g/mol
Topological Polar Surface Area (TPSA) 40.80 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.40
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Benzo(g)-1,3-benzodioxolo(5,6-a)quinolizinium, 5,6-dihydro-9,10-dimethoxy-13-methyl-
38691-92-8
SCHEMBL299398
CHEMBL1186429
DTXSID40191981
PD057726

2D Structure

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2D Structure of Benzo(g)-1,3-benzodioxolo(5,6-a)quinolizinium, 5,6-dihydro-9,10-dimethoxy-13-methyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5830 58.30%
Caco-2 + 0.9423 94.23%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4565 45.65%
OATP2B1 inhibitior - 0.8994 89.94%
OATP1B1 inhibitior + 0.9295 92.95%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.5152 51.52%
BSEP inhibitior + 0.8034 80.34%
P-glycoprotein inhibitior + 0.7416 74.16%
P-glycoprotein substrate - 0.7600 76.00%
CYP3A4 substrate + 0.6076 60.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7332 73.32%
CYP3A4 inhibition - 0.6606 66.06%
CYP2C9 inhibition - 0.8795 87.95%
CYP2C19 inhibition - 0.6564 65.64%
CYP2D6 inhibition + 0.8014 80.14%
CYP1A2 inhibition + 0.7753 77.53%
CYP2C8 inhibition - 0.5892 58.92%
CYP inhibitory promiscuity + 0.8776 87.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4626 46.26%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.9101 91.01%
Skin irritation - 0.7912 79.12%
Skin corrosion - 0.9428 94.28%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4522 45.22%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8709 87.09%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8305 83.05%
Acute Oral Toxicity (c) III 0.6283 62.83%
Estrogen receptor binding + 0.9236 92.36%
Androgen receptor binding + 0.6678 66.78%
Thyroid receptor binding + 0.6669 66.69%
Glucocorticoid receptor binding + 0.8548 85.48%
Aromatase binding - 0.6799 67.99%
PPAR gamma + 0.7455 74.55%
Honey bee toxicity - 0.7811 78.11%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity - 0.5599 55.99%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.88% 96.77%
CHEMBL1951 P21397 Monoamine oxidase A 94.62% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.36% 95.56%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 92.23% 96.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.20% 91.11%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.91% 89.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.93% 93.99%
CHEMBL2581 P07339 Cathepsin D 87.69% 98.95%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 87.62% 82.67%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.17% 94.80%
CHEMBL261 P00915 Carbonic anhydrase I 86.92% 96.76%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.86% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.54% 94.45%
CHEMBL2535 P11166 Glucose transporter 86.05% 98.75%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 85.37% 94.03%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.10% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.21% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.42% 86.33%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 82.87% 92.38%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.85% 93.40%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.69% 92.62%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.87% 83.57%
CHEMBL5747 Q92793 CREB-binding protein 81.73% 95.12%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.58% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.89% 99.17%

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.
Coptis chinensis
Coptis deltoidea
Coptis japonica
Coptis teeta
Corydalis solida

Cross-Links

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PubChem 148262
NPASS NPC186733
LOTUS LTS0216467
wikiData Q83064564