6-methoxy-3-methyl-9H-carbazol-2-ol

Details

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Internal ID 0fb32092-a499-4810-940c-d3453b99dafc
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 6-methoxy-3-methyl-9H-carbazol-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H13NO2/c1-8-5-10-11-6-9(17-2)3-4-12(11)15-13(10)7-14(8)16/h3-7,15-16H,1-2H3
InChI Key AIVUYXSNEZKNBV-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C14H13NO2
Molecular Weight 227.26 g/mol
Exact Mass 227.094628657 g/mol
Topological Polar Surface Area (TPSA) 45.30 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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6-methoxy-3-methyl-9H-carbazol-2-ol
CHEMBL4080182

2D Structure

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2D Structure of 6-methoxy-3-methyl-9H-carbazol-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.5190 51.90%
Blood Brain Barrier + 0.6629 66.29%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6796 67.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8896 88.96%
OATP1B3 inhibitior + 0.9499 94.99%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.5927 59.27%
P-glycoprotein inhibitior - 0.9277 92.77%
P-glycoprotein substrate - 0.8704 87.04%
CYP3A4 substrate - 0.5471 54.71%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.7074 70.74%
CYP3A4 inhibition + 0.6881 68.81%
CYP2C9 inhibition + 0.7808 78.08%
CYP2C19 inhibition + 0.7994 79.94%
CYP2D6 inhibition + 0.6260 62.60%
CYP1A2 inhibition + 0.9148 91.48%
CYP2C8 inhibition - 0.6439 64.39%
CYP inhibitory promiscuity + 0.8997 89.97%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8810 88.10%
Carcinogenicity (trinary) Non-required 0.4065 40.65%
Eye corrosion - 0.9936 99.36%
Eye irritation + 0.9531 95.31%
Skin irritation - 0.8579 85.79%
Skin corrosion - 0.9355 93.55%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5987 59.87%
Micronuclear + 0.7459 74.59%
Hepatotoxicity - 0.5435 54.35%
skin sensitisation - 0.8684 86.84%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.7706 77.06%
Acute Oral Toxicity (c) III 0.5988 59.88%
Estrogen receptor binding + 0.9257 92.57%
Androgen receptor binding + 0.7689 76.89%
Thyroid receptor binding + 0.7372 73.72%
Glucocorticoid receptor binding + 0.8651 86.51%
Aromatase binding + 0.8580 85.80%
PPAR gamma + 0.7177 71.77%
Honey bee toxicity - 0.9616 96.16%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.4738 47.38%

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 98.68% 91.11%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 94.72% 91.79%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.48% 93.99%
CHEMBL1951 P21397 Monoamine oxidase A 93.56% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.39% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.31% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.39% 99.15%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 91.88% 93.24%
CHEMBL4208 P20618 Proteasome component C5 90.73% 90.00%
CHEMBL2535 P11166 Glucose transporter 90.19% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.98% 94.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 89.43% 91.71%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 88.51% 95.70%
CHEMBL1907 P15144 Aminopeptidase N 87.97% 93.31%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.84% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.18% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.69% 86.92%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 82.52% 85.49%

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.
Glycosmis pentaphylla

Cross-Links

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PubChem 10353687
LOTUS LTS0159954
wikiData Q104912989