6-Oxomethuenine

Details

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Internal ID cf8ade7b-2425-4b03-941a-4270dbd95bde
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles
IUPAC Name (3S,7E,8R)-7-ethylidene-5-methyl-5,12-diazatetracyclo[9.7.0.03,8.013,18]octadeca-1(11),13,15,17-tetraene-2,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H20N2O2/c1-3-11-9-21(2)10-14-13(11)8-16(22)18-17(19(14)23)12-6-4-5-7-15(12)20-18/h3-7,13-14,20H,8-10H2,1-2H3/b11-3-/t13-,14+/m0/s1
InChI Key QRIDDVDKSXHDHM-FGYBBMNVSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20N2O2
Molecular Weight 308.40 g/mol
Exact Mass 308.152477885 g/mol
Topological Polar Surface Area (TPSA) 53.20 Ų
XlogP 2.00
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEMBL487403

2D Structure

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2D Structure of 6-Oxomethuenine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.9148 91.48%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6076 60.76%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.8715 87.15%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.5410 54.10%
P-glycoprotein inhibitior - 0.6244 62.44%
P-glycoprotein substrate - 0.6994 69.94%
CYP3A4 substrate + 0.5999 59.99%
CYP2C9 substrate - 0.5564 55.64%
CYP2D6 substrate - 0.6939 69.39%
CYP3A4 inhibition - 0.8203 82.03%
CYP2C9 inhibition - 0.8178 81.78%
CYP2C19 inhibition - 0.7358 73.58%
CYP2D6 inhibition - 0.6612 66.12%
CYP1A2 inhibition - 0.6048 60.48%
CYP2C8 inhibition - 0.7723 77.23%
CYP inhibitory promiscuity - 0.7780 77.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6205 62.05%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9916 99.16%
Skin irritation - 0.7766 77.66%
Skin corrosion - 0.9275 92.75%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8832 88.32%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.5909 59.09%
skin sensitisation - 0.8520 85.20%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.5610 56.10%
Acute Oral Toxicity (c) III 0.5884 58.84%
Estrogen receptor binding - 0.5994 59.94%
Androgen receptor binding + 0.8011 80.11%
Thyroid receptor binding - 0.5347 53.47%
Glucocorticoid receptor binding + 0.5386 53.86%
Aromatase binding - 0.6118 61.18%
PPAR gamma + 0.5261 52.61%
Honey bee toxicity - 0.9247 92.47%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.8999 89.99%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.04% 95.56%
CHEMBL2581 P07339 Cathepsin D 97.53% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.82% 93.99%
CHEMBL255 P29275 Adenosine A2b receptor 93.30% 98.59%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.94% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.21% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.91% 89.00%
CHEMBL3310 Q96DB2 Histone deacetylase 11 87.76% 88.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.66% 99.23%
CHEMBL321 P14780 Matrix metalloproteinase 9 83.88% 92.12%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.96% 90.08%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.86% 97.09%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.81% 93.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.63% 97.25%
CHEMBL2535 P11166 Glucose transporter 80.58% 98.75%

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.
Tabernaemontana inconspicua
Tabernaemontana pauciflora

Cross-Links

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PubChem 14707495
LOTUS LTS0120626
wikiData Q104396821