Dehydrocoreximine

Details

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Internal ID 51e71621-5a50-4268-9bb2-12957bd80aec
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Isoquinolones and derivatives
IUPAC Name 2-hydroxy-3,10-dimethoxy-6,7-dihydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-11-one
SMILES (Canonical) COC1=CC2=C[NH+]3CCC4=CC(=C(C=C4C3=CC2=CC1=O)O)OC
SMILES (Isomeric) COC1=CC2=C[NH+]3CCC4=CC(=C(C=C4C3=CC2=CC1=O)O)OC
InChI InChI=1S/C19H17NO4/c1-23-18-7-11-3-4-20-10-13-8-19(24-2)16(21)6-12(13)5-15(20)14(11)9-17(18)22/h5-10,22H,3-4H2,1-2H3/p+1
InChI Key JINZPDPFJUIUQY-UHFFFAOYSA-O
Popularity 1 reference 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 2.10
Atomic LogP (AlogP) 1.12
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 Dehydrocoreximine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8301 83.01%
Caco-2 + 0.9093 90.93%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5419 54.19%
OATP2B1 inhibitior - 0.8620 86.20%
OATP1B1 inhibitior + 0.9293 92.93%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7786 77.86%
P-glycoprotein inhibitior - 0.4385 43.85%
P-glycoprotein substrate - 0.7190 71.90%
CYP3A4 substrate + 0.5892 58.92%
CYP2C9 substrate - 0.8109 81.09%
CYP2D6 substrate - 0.7039 70.39%
CYP3A4 inhibition - 0.8503 85.03%
CYP2C9 inhibition - 0.7683 76.83%
CYP2C19 inhibition - 0.7892 78.92%
CYP2D6 inhibition + 0.5000 50.00%
CYP1A2 inhibition - 0.5385 53.85%
CYP2C8 inhibition + 0.4433 44.33%
CYP inhibitory promiscuity - 0.6953 69.53%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6289 62.89%
Eye corrosion - 0.9810 98.10%
Eye irritation - 0.8925 89.25%
Skin irritation - 0.7250 72.50%
Skin corrosion - 0.9237 92.37%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6614 66.14%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8440 84.40%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.4735 47.35%
Acute Oral Toxicity (c) III 0.6071 60.71%
Estrogen receptor binding + 0.9398 93.98%
Androgen receptor binding - 0.5224 52.24%
Thyroid receptor binding + 0.6547 65.47%
Glucocorticoid receptor binding + 0.8642 86.42%
Aromatase binding + 0.7181 71.81%
PPAR gamma + 0.7577 75.77%
Honey bee toxicity - 0.7817 78.17%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5349 53.49%
Fish aquatic toxicity - 0.5592 55.92%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.64% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.24% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 93.24% 93.40%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.02% 86.33%
CHEMBL4208 P20618 Proteasome component C5 91.35% 90.00%
CHEMBL2535 P11166 Glucose transporter 91.33% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.04% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.03% 92.94%
CHEMBL2581 P07339 Cathepsin D 89.65% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.37% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.69% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 86.44% 91.49%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.80% 96.77%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.75% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.21% 85.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.91% 95.89%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.96% 92.38%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.72% 93.03%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.46% 89.00%

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.
Annona squamosa

Cross-Links

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PubChem 101731565
NPASS NPC19722