8,8''-Biskoenigine

Details

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Internal ID e4b08bcb-859d-4db6-ac1f-d2566958eb35
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 10-(9-hydroxy-8-methoxy-3,3,5-trimethyl-11H-pyrano[3,2-a]carbazol-10-yl)-8-methoxy-3,3,5-trimethyl-11H-pyrano[3,2-a]carbazol-9-ol
SMILES (Canonical) CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C(C(=C(C=C24)OC)O)C5=C6C(=CC(=C5O)OC)C7=C(N6)C8=C(C(=C7)C)OC(C=C8)(C)C
SMILES (Isomeric) CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=C(C(=C(C=C24)OC)O)C5=C6C(=CC(=C5O)OC)C7=C(N6)C8=C(C(=C7)C)OC(C=C8)(C)C
InChI InChI=1S/C38H36N2O6/c1-17-13-21-23-15-25(43-7)33(41)27(31(23)39-29(21)19-9-11-37(3,4)45-35(17)19)28-32-24(16-26(44-8)34(28)42)22-14-18(2)36-20(30(22)40-32)10-12-38(5,6)46-36/h9-16,39-42H,1-8H3
InChI Key DQRAEENKHHFBHV-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C38H36N2O6
Molecular Weight 616.70 g/mol
Exact Mass 616.25733687 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 8.30
Atomic LogP (AlogP) 9.04
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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CHEMBL434383
477890-82-7
8,8'-Biskoenigine
8,8''''-Biskoenigine
SCHEMBL12069529
BDBM50476091
AKOS040763250

2D Structure

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2D Structure of 8,8''-Biskoenigine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9686 96.86%
Caco-2 - 0.7866 78.66%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6363 63.63%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.8410 84.10%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9336 93.36%
P-glycoprotein inhibitior + 0.8450 84.50%
P-glycoprotein substrate - 0.6156 61.56%
CYP3A4 substrate + 0.5966 59.66%
CYP2C9 substrate + 0.6048 60.48%
CYP2D6 substrate - 0.7630 76.30%
CYP3A4 inhibition + 0.8703 87.03%
CYP2C9 inhibition + 0.7380 73.80%
CYP2C19 inhibition + 0.8367 83.67%
CYP2D6 inhibition - 0.5825 58.25%
CYP1A2 inhibition + 0.6564 65.64%
CYP2C8 inhibition + 0.7652 76.52%
CYP inhibitory promiscuity + 0.9566 95.66%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.5197 51.97%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.7399 73.99%
Skin irritation - 0.8301 83.01%
Skin corrosion - 0.9358 93.58%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6827 68.27%
Micronuclear + 0.7600 76.00%
Hepatotoxicity - 0.6237 62.37%
skin sensitisation - 0.8640 86.40%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8626 86.26%
Acute Oral Toxicity (c) III 0.5634 56.34%
Estrogen receptor binding + 0.8377 83.77%
Androgen receptor binding + 0.6607 66.07%
Thyroid receptor binding + 0.7486 74.86%
Glucocorticoid receptor binding + 0.7658 76.58%
Aromatase binding + 0.6836 68.36%
PPAR gamma + 0.7259 72.59%
Honey bee toxicity - 0.8624 86.24%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8085 80.85%

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 99.01% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.35% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.92% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.70% 96.09%
CHEMBL213 P08588 Beta-1 adrenergic receptor 92.05% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.56% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 89.46% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.10% 89.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 86.78% 96.21%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.44% 89.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.40% 86.33%
CHEMBL2535 P11166 Glucose transporter 86.05% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.98% 99.15%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.83% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 84.26% 94.73%
CHEMBL4208 P20618 Proteasome component C5 83.68% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.46% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.90% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 82.80% 90.20%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.71% 92.62%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.63% 85.49%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 81.55% 93.24%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.42% 93.99%
CHEMBL2581 P07339 Cathepsin D 80.63% 98.95%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 80.32% 95.34%
CHEMBL290 Q13370 Phosphodiesterase 3B 80.24% 94.00%

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.
Murraya koenigii

Cross-Links

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PubChem 12967046
NPASS NPC277351
LOTUS LTS0269030
wikiData Q104987088