N-methoxy-3-hydroxymethylcarbazole

Details

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Internal ID ebec3b19-5c59-4330-89c6-c0af1ca899b1
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name (9-methoxycarbazol-3-yl)methanol
SMILES (Canonical) CON1C2=C(C=C(C=C2)CO)C3=CC=CC=C31
SMILES (Isomeric) CON1C2=C(C=C(C=C2)CO)C3=CC=CC=C31
InChI InChI=1S/C14H13NO2/c1-17-15-13-5-3-2-4-11(13)12-8-10(9-16)6-7-14(12)15/h2-8,16H,9H2,1H3
InChI Key OGVBLMOKWOEKIO-UHFFFAOYSA-N
Popularity 2 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) 34.40 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.35
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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142768-49-8
orb1680552
AKOS040763244
H62972

2D Structure

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2D Structure of N-methoxy-3-hydroxymethylcarbazole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.7080 70.80%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.5435 54.35%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8974 89.74%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7390 73.90%
P-glycoprotein inhibitior - 0.9308 93.08%
P-glycoprotein substrate - 0.8231 82.31%
CYP3A4 substrate - 0.5318 53.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7235 72.35%
CYP3A4 inhibition - 0.8078 80.78%
CYP2C9 inhibition - 0.5633 56.33%
CYP2C19 inhibition - 0.5286 52.86%
CYP2D6 inhibition - 0.8345 83.45%
CYP1A2 inhibition + 0.8146 81.46%
CYP2C8 inhibition - 0.5858 58.58%
CYP inhibitory promiscuity + 0.6316 63.16%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8408 84.08%
Carcinogenicity (trinary) Non-required 0.4121 41.21%
Eye corrosion - 0.9777 97.77%
Eye irritation + 0.8333 83.33%
Skin irritation - 0.7744 77.44%
Skin corrosion - 0.9382 93.82%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6613 66.13%
Micronuclear + 0.7159 71.59%
Hepatotoxicity + 0.5018 50.18%
skin sensitisation - 0.8182 81.82%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.8912 89.12%
Acute Oral Toxicity (c) III 0.6600 66.00%
Estrogen receptor binding + 0.9120 91.20%
Androgen receptor binding + 0.6524 65.24%
Thyroid receptor binding + 0.6158 61.58%
Glucocorticoid receptor binding + 0.7039 70.39%
Aromatase binding + 0.7510 75.10%
PPAR gamma + 0.6338 63.38%
Honey bee toxicity - 0.8523 85.23%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity - 0.4941 49.41%

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
CHEMBL2581 P07339 Cathepsin D 96.15% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.06% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.44% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.72% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.49% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.45% 86.33%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 85.28% 85.49%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 83.59% 92.67%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 82.78% 89.44%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.68% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.52% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.06% 91.71%

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.
Bergera euchrestifolia

Cross-Links

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PubChem 15161588
LOTUS LTS0230827
wikiData Q105191880