Drimaritin

Details

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Internal ID f39a51b3-3ac6-49c2-99fa-385e3a3b68da
Taxonomy Alkaloids and derivatives > Indolonaphthyridine alkaloids
IUPAC Name 3-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-2,5,7,9(16),10,12,14-heptaen-4-one
SMILES (Canonical) COC1=CN2C3=CC=CC=C3C4=C2C(=NC=C4)C1=O
SMILES (Isomeric) COC1=CN2C3=CC=CC=C3C4=C2C(=NC=C4)C1=O
InChI InChI=1S/C15H10N2O2/c1-19-12-8-17-11-5-3-2-4-9(11)10-6-7-16-13(14(10)17)15(12)18/h2-8H,1H3
InChI Key ARKHSSXCCQCKAF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H10N2O2
Molecular Weight 250.25 g/mol
Exact Mass 250.074227566 g/mol
Topological Polar Surface Area (TPSA) 44.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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CHEMBL517641
4H-Indolo[3,2,1-de][1,5]naphthyridin-4-one, 5-methoxy-

2D Structure

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2D Structure of Drimaritin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.7883 78.83%
Blood Brain Barrier + 0.9196 91.96%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.8491 84.91%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9724 97.24%
OATP1B3 inhibitior + 0.9637 96.37%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7848 78.48%
BSEP inhibitior + 0.6219 62.19%
P-glycoprotein inhibitior - 0.7481 74.81%
P-glycoprotein substrate - 0.7265 72.65%
CYP3A4 substrate + 0.5663 56.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8260 82.60%
CYP3A4 inhibition + 0.6167 61.67%
CYP2C9 inhibition - 0.7826 78.26%
CYP2C19 inhibition + 0.7012 70.12%
CYP2D6 inhibition - 0.7308 73.08%
CYP1A2 inhibition + 0.9667 96.67%
CYP2C8 inhibition - 0.7499 74.99%
CYP inhibitory promiscuity + 0.8382 83.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4443 44.43%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.8232 82.32%
Skin irritation - 0.8116 81.16%
Skin corrosion - 0.9632 96.32%
Ames mutagenesis + 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6841 68.41%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.9047 90.47%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7021 70.21%
Acute Oral Toxicity (c) III 0.6322 63.22%
Estrogen receptor binding + 0.6478 64.78%
Androgen receptor binding - 0.5255 52.55%
Thyroid receptor binding + 0.5829 58.29%
Glucocorticoid receptor binding + 0.8846 88.46%
Aromatase binding + 0.8565 85.65%
PPAR gamma - 0.6222 62.22%
Honey bee toxicity - 0.8725 87.25%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.6187 61.87%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.06% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.25% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.08% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.96% 89.00%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 92.79% 96.47%
CHEMBL3192 Q9BY41 Histone deacetylase 8 92.45% 93.99%
CHEMBL2581 P07339 Cathepsin D 92.15% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.96% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.11% 94.00%
CHEMBL2535 P11166 Glucose transporter 86.47% 98.75%
CHEMBL2094121 P14867 GABA-A receptor; alpha-1/beta-3/gamma-2 85.60% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.24% 86.33%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 84.85% 92.67%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 84.14% 96.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.24% 96.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.25% 96.67%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 81.67% 100.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.19% 89.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.56% 91.11%

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.
Drymaria cordata

Cross-Links

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PubChem 3012902
NPASS NPC81535
LOTUS LTS0039220
wikiData Q104917394