1-(methoxymethyl)-carbazomycin B

Details

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Internal ID 2ec4c03e-1fe6-4f69-ad31-3dab5fb31c80
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 3-methoxy-1-(methoxymethyl)-2-methyl-9H-carbazol-4-ol
SMILES (Canonical) CC1=C(C2=C(C3=CC=CC=C3N2)C(=C1OC)O)COC
SMILES (Isomeric) CC1=C(C2=C(C3=CC=CC=C3N2)C(=C1OC)O)COC
InChI InChI=1S/C16H17NO3/c1-9-11(8-19-2)14-13(15(18)16(9)20-3)10-6-4-5-7-12(10)17-14/h4-7,17-18H,8H2,1-3H3
InChI Key VNJYWRJORLUTMB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H17NO3
Molecular Weight 271.31 g/mol
Exact Mass 271.12084340 g/mol
Topological Polar Surface Area (TPSA) 54.50 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(methoxymethyl)-carbazomycin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.7541 75.41%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6057 60.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7187 71.87%
OATP1B3 inhibitior + 0.9232 92.32%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.5697 56.97%
P-glycoprotein inhibitior - 0.8664 86.64%
P-glycoprotein substrate - 0.7808 78.08%
CYP3A4 substrate + 0.5862 58.62%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.7224 72.24%
CYP3A4 inhibition + 0.7436 74.36%
CYP2C9 inhibition + 0.5193 51.93%
CYP2C19 inhibition + 0.7072 70.72%
CYP2D6 inhibition - 0.5186 51.86%
CYP1A2 inhibition + 0.8278 82.78%
CYP2C8 inhibition + 0.8302 83.02%
CYP inhibitory promiscuity + 0.8170 81.70%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9710 97.10%
Carcinogenicity (trinary) Non-required 0.5658 56.58%
Eye corrosion - 0.9917 99.17%
Eye irritation + 0.7008 70.08%
Skin irritation - 0.8245 82.45%
Skin corrosion - 0.9400 94.00%
Ames mutagenesis + 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5251 52.51%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation - 0.8341 83.41%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8953 89.53%
Acute Oral Toxicity (c) III 0.6337 63.37%
Estrogen receptor binding + 0.7572 75.72%
Androgen receptor binding + 0.5417 54.17%
Thyroid receptor binding + 0.6652 66.52%
Glucocorticoid receptor binding + 0.8037 80.37%
Aromatase binding + 0.7987 79.87%
PPAR gamma + 0.7725 77.25%
Honey bee toxicity - 0.9297 92.97%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.8081 80.81%

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 97.92% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.39% 95.56%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 92.10% 91.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.89% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.78% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.11% 94.00%
CHEMBL213 P08588 Beta-1 adrenergic receptor 88.97% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.34% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.41% 93.99%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.15% 85.14%
CHEMBL2885 P07451 Carbonic anhydrase III 84.00% 87.45%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 83.73% 93.24%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 82.05% 91.79%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.80% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.77% 99.17%
CHEMBL1937 Q92769 Histone deacetylase 2 81.69% 94.75%
CHEMBL2535 P11166 Glucose transporter 81.49% 98.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139587724
LOTUS LTS0062889
wikiData Q77572675