Korupensamine C

Details

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Internal ID 20e1d669-6d8c-4aad-91ca-210cb45c54a0
Taxonomy Organoheterocyclic compounds > Isoquinolines and derivatives > Naphthylisoquinolines
IUPAC Name (1R,3R)-5-(4,5-dimethoxy-7-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinoline-6,8-diol
SMILES (Canonical) CC1CC2=C(C(=CC(=C2C(N1)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C
SMILES (Isomeric) C[C@@H]1CC2=C(C(=CC(=C2[C@H](N1)C)O)O)C3=C4C=C(C=C(C4=C(C=C3)OC)OC)C
InChI InChI=1S/C24H27NO4/c1-12-8-16-15(6-7-20(28-4)24(16)21(9-12)29-5)23-17-10-13(2)25-14(3)22(17)18(26)11-19(23)27/h6-9,11,13-14,25-27H,10H2,1-5H3/t13-,14-/m1/s1
InChI Key PLLKZICNVDBVIE-ZIAGYGMSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H27NO4
Molecular Weight 393.50 g/mol
Exact Mass 393.19400834 g/mol
Topological Polar Surface Area (TPSA) 71.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.84
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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NSC692900
NSC-692900

2D Structure

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2D Structure of Korupensamine C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9655 96.55%
Caco-2 + 0.7196 71.96%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4319 43.19%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.8681 86.81%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8361 83.61%
BSEP inhibitior + 0.8971 89.71%
P-glycoprotein inhibitior - 0.4937 49.37%
P-glycoprotein substrate + 0.5505 55.05%
CYP3A4 substrate + 0.6296 62.96%
CYP2C9 substrate - 0.7713 77.13%
CYP2D6 substrate + 0.7329 73.29%
CYP3A4 inhibition - 0.6221 62.21%
CYP2C9 inhibition - 0.5569 55.69%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition + 0.5968 59.68%
CYP1A2 inhibition - 0.7143 71.43%
CYP2C8 inhibition + 0.7181 71.81%
CYP inhibitory promiscuity + 0.6300 63.00%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5600 56.00%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.8145 81.45%
Skin irritation - 0.8266 82.66%
Skin corrosion - 0.9088 90.88%
Ames mutagenesis + 0.5663 56.63%
Human Ether-a-go-go-Related Gene inhibition + 0.7730 77.30%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.6061 60.61%
skin sensitisation - 0.9174 91.74%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.8409 84.09%
Acute Oral Toxicity (c) III 0.5077 50.77%
Estrogen receptor binding + 0.7733 77.33%
Androgen receptor binding + 0.6457 64.57%
Thyroid receptor binding + 0.7186 71.86%
Glucocorticoid receptor binding + 0.6417 64.17%
Aromatase binding + 0.5474 54.74%
PPAR gamma + 0.6988 69.88%
Honey bee toxicity - 0.8023 80.23%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity - 0.3647 36.47%

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
CHEMBL1951 P21397 Monoamine oxidase A 99.15% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.40% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.06% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 95.27% 92.94%
CHEMBL2581 P07339 Cathepsin D 93.55% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.48% 95.56%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 93.22% 91.79%
CHEMBL2535 P11166 Glucose transporter 92.19% 98.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 90.86% 96.21%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 90.51% 97.31%
CHEMBL213 P08588 Beta-1 adrenergic receptor 89.91% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.09% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.76% 89.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.37% 89.62%
CHEMBL4208 P20618 Proteasome component C5 88.20% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.37% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.13% 94.00%
CHEMBL5747 Q92793 CREB-binding protein 85.59% 95.12%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.18% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.97% 93.03%
CHEMBL3438 Q05513 Protein kinase C zeta 83.66% 88.48%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.32% 90.24%
CHEMBL2056 P21728 Dopamine D1 receptor 82.95% 91.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.13% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.78% 99.15%
CHEMBL4630 O14757 Serine/threonine-protein kinase Chk1 81.33% 97.03%
CHEMBL2243 O00519 Anandamide amidohydrolase 81.31% 97.53%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.89% 99.17%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.51% 96.67%

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.
Ancistrocladus korupensis

Cross-Links

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PubChem 392422
LOTUS LTS0015815
wikiData Q105211023