Demethyl eneberberine

Details

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Internal ID 27b86927-0b71-4fb9-bccc-5f24ac424eee
Taxonomy Alkaloids and derivatives > Protoberberine alkaloids and derivatives
IUPAC Name 2-hydroxy-9,10-dimethoxy-6,7-dihydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-3-one
SMILES (Canonical) COC1=C(C2=C[NH+]3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)O)OC
SMILES (Isomeric) COC1=C(C2=C[NH+]3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)O)OC
InChI InChI=1S/C19H17NO4/c1-23-18-4-3-11-7-15-13-9-17(22)16(21)8-12(13)5-6-20(15)10-14(11)19(18)24-2/h3-4,7-10,22H,5-6H2,1-2H3/p+1
InChI Key HVTCKKMWZDDWOY-UHFFFAOYSA-O
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18NO4+
Molecular Weight 324.30 g/mol
Exact Mass 324.12358306 g/mol
Topological Polar Surface Area (TPSA) 60.20 Ų
XlogP 1.10
Atomic LogP (AlogP) -0.27
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Demethyl eneberberine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8144 81.44%
Caco-2 + 0.7987 79.87%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6389 63.89%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.9229 92.29%
OATP1B3 inhibitior + 0.9482 94.82%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7352 73.52%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.7297 72.97%
CYP3A4 substrate + 0.6105 61.05%
CYP2C9 substrate - 0.8087 80.87%
CYP2D6 substrate - 0.6878 68.78%
CYP3A4 inhibition - 0.8649 86.49%
CYP2C9 inhibition - 0.7957 79.57%
CYP2C19 inhibition - 0.7814 78.14%
CYP2D6 inhibition - 0.5096 50.96%
CYP1A2 inhibition - 0.5732 57.32%
CYP2C8 inhibition + 0.4605 46.05%
CYP inhibitory promiscuity - 0.7027 70.27%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6011 60.11%
Eye corrosion - 0.9817 98.17%
Eye irritation - 0.8301 83.01%
Skin irritation - 0.7379 73.79%
Skin corrosion - 0.9262 92.62%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6506 65.06%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8472 84.72%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.6529 65.29%
Acute Oral Toxicity (c) III 0.6265 62.65%
Estrogen receptor binding + 0.8949 89.49%
Androgen receptor binding + 0.6633 66.33%
Thyroid receptor binding + 0.7251 72.51%
Glucocorticoid receptor binding + 0.8996 89.96%
Aromatase binding + 0.6881 68.81%
PPAR gamma + 0.8561 85.61%
Honey bee toxicity - 0.8154 81.54%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.5712 57.12%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.75% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.02% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.41% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.80% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.73% 85.14%
CHEMBL2535 P11166 Glucose transporter 87.23% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.38% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.70% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.69% 94.00%
CHEMBL4208 P20618 Proteasome component C5 84.34% 90.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.90% 91.11%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.69% 86.92%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.47% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.86% 95.89%

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
Phellodendron amurense
Phellodendron chinense
Tinospora sagittata

Cross-Links

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PubChem 101404949
NPASS NPC44101