7-hydroxy-3-methoxy-6-methyl-9H-carbazole-1,4-dione

Details

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Internal ID 8551f083-d92d-46f2-af89-f63297715e34
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 7-hydroxy-3-methoxy-6-methyl-9H-carbazole-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H11NO4/c1-6-3-7-8(4-9(6)16)15-13-10(17)5-11(19-2)14(18)12(7)13/h3-5,15-16H,1-2H3
InChI Key VREJGEPSCUUWMS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H11NO4
Molecular Weight 257.24 g/mol
Exact Mass 257.06880783 g/mol
Topological Polar Surface Area (TPSA) 79.40 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-hydroxy-3-methoxy-6-methyl-9H-carbazole-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 - 0.5491 54.91%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.5488 54.88%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9173 91.73%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7146 71.46%
P-glycoprotein inhibitior - 0.9186 91.86%
P-glycoprotein substrate - 0.9091 90.91%
CYP3A4 substrate + 0.5154 51.54%
CYP2C9 substrate + 0.5905 59.05%
CYP2D6 substrate - 0.8674 86.74%
CYP3A4 inhibition - 0.5095 50.95%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.5398 53.98%
CYP2D6 inhibition - 0.7682 76.82%
CYP1A2 inhibition + 0.7632 76.32%
CYP2C8 inhibition + 0.4539 45.39%
CYP inhibitory promiscuity + 0.8498 84.98%
UGT catelyzed - 0.6638 66.38%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Non-required 0.4550 45.50%
Eye corrosion - 0.9923 99.23%
Eye irritation + 0.8868 88.68%
Skin irritation - 0.8524 85.24%
Skin corrosion - 0.9463 94.63%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7726 77.26%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8776 87.76%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6081 60.81%
Acute Oral Toxicity (c) III 0.5510 55.10%
Estrogen receptor binding + 0.7018 70.18%
Androgen receptor binding + 0.6668 66.68%
Thyroid receptor binding - 0.5983 59.83%
Glucocorticoid receptor binding + 0.6225 62.25%
Aromatase binding + 0.7026 70.26%
PPAR gamma + 0.6778 67.78%
Honey bee toxicity - 0.9105 91.05%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.8783 87.83%

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 97.70% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.35% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.01% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.15% 93.99%
CHEMBL2581 P07339 Cathepsin D 92.05% 98.95%
CHEMBL2535 P11166 Glucose transporter 91.28% 98.75%
CHEMBL1951 P21397 Monoamine oxidase A 91.22% 91.49%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 90.37% 92.68%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.73% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.00% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.41% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 86.85% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.71% 94.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.80% 93.40%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.48% 91.71%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 81.44% 95.70%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.08% 96.67%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.45% 96.00%

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.
Clausena excavata

Cross-Links

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PubChem 44317062
LOTUS LTS0231845
wikiData Q105291709