7-Hydroxytryptanthrin

Details

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Internal ID 67624914-c744-483f-9281-6093d41dd458
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinazolines > Indoloquinazolines
IUPAC Name 7-hydroxyindolo[2,1-b]quinazoline-6,12-dione
SMILES (Canonical) C1=CC=C2C(=C1)C(=O)N3C4=C(C(=CC=C4)O)C(=O)C3=N2
SMILES (Isomeric) C1=CC=C2C(=C1)C(=O)N3C4=C(C(=CC=C4)O)C(=O)C3=N2
InChI InChI=1S/C15H8N2O3/c18-11-7-3-6-10-12(11)13(19)14-16-9-5-2-1-4-8(9)15(20)17(10)14/h1-7,18H
InChI Key WOQXYBJCORZEEE-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H8N2O3
Molecular Weight 264.23 g/mol
Exact Mass 264.05349212 g/mol
Topological Polar Surface Area (TPSA) 70.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.64
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEMBL452806

2D Structure

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2D Structure of 7-Hydroxytryptanthrin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.6087 60.87%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7683 76.83%
OATP2B1 inhibitior - 0.7214 72.14%
OATP1B1 inhibitior + 0.9401 94.01%
OATP1B3 inhibitior + 0.9504 95.04%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9566 95.66%
BSEP inhibitior - 0.7580 75.80%
P-glycoprotein inhibitior - 0.8922 89.22%
P-glycoprotein substrate - 0.9660 96.60%
CYP3A4 substrate + 0.5143 51.43%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8751 87.51%
CYP3A4 inhibition - 0.9301 93.01%
CYP2C9 inhibition + 0.5058 50.58%
CYP2C19 inhibition - 0.6088 60.88%
CYP2D6 inhibition - 0.7878 78.78%
CYP1A2 inhibition + 0.5731 57.31%
CYP2C8 inhibition + 0.4577 45.77%
CYP inhibitory promiscuity - 0.8596 85.96%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5186 51.86%
Eye corrosion - 0.9903 99.03%
Eye irritation + 0.5997 59.97%
Skin irritation - 0.8585 85.85%
Skin corrosion - 0.9724 97.24%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8759 87.59%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.9386 93.86%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) II 0.4490 44.90%
Estrogen receptor binding + 0.6993 69.93%
Androgen receptor binding - 0.5169 51.69%
Thyroid receptor binding + 0.5692 56.92%
Glucocorticoid receptor binding + 0.8977 89.77%
Aromatase binding + 0.8257 82.57%
PPAR gamma + 0.8022 80.22%
Honey bee toxicity - 0.9549 95.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.5883 58.83%

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 97.18% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 97.01% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.90% 85.14%
CHEMBL2581 P07339 Cathepsin D 94.12% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 92.34% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.76% 99.15%
CHEMBL5805 Q9NR97 Toll-like receptor 8 88.51% 96.25%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 88.33% 98.46%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.20% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.50% 94.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.07% 89.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.84% 96.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.14% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.57% 93.99%
CHEMBL1781 P11387 DNA topoisomerase I 84.48% 97.00%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 83.18% 96.47%
CHEMBL1937 Q92769 Histone deacetylase 2 83.17% 94.75%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.20% 92.67%

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.
Phaius mishmensis

Cross-Links

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PubChem 24970644
LOTUS LTS0214901
wikiData Q105309648