delta-Indomycinone

Details

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Internal ID ad753f87-ed15-4d3b-ac76-0c025ef5b87d
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 2-(2,5-dihydroxyhexan-2-yl)-11-hydroxy-5-methylnaphtho[2,3-h]chromene-4,7,12-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H22O7/c1-11-9-14-20(22(29)19-13(21(14)28)5-4-6-15(19)26)23-18(11)16(27)10-17(31-23)24(3,30)8-7-12(2)25/h4-6,9-10,12,25-26,30H,7-8H2,1-3H3
InChI Key COXIHEKDXQWYGL-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C24H22O7
Molecular Weight 422.40 g/mol
Exact Mass 422.13655304 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.95
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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2-(2,5-Dihydroxyhexan-2-yl)-11-hydroxy-5-methylnaphtho[2,3-h]chromene-4,7,12-trione
2-(2,5-dihydroxyhexan-2-yl)-11-hydroxy-5-methylnaphtho(2,3-h)chromene-4,7,12-trione
RefChem:131681
CHEBI:206260

2D Structure

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2D Structure of delta-Indomycinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9773 97.73%
Caco-2 - 0.6419 64.19%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6891 68.91%
OATP2B1 inhibitior - 0.5693 56.93%
OATP1B1 inhibitior + 0.8933 89.33%
OATP1B3 inhibitior + 0.9197 91.97%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7367 73.67%
P-glycoprotein inhibitior - 0.6117 61.17%
P-glycoprotein substrate + 0.5451 54.51%
CYP3A4 substrate + 0.6049 60.49%
CYP2C9 substrate + 0.5853 58.53%
CYP2D6 substrate - 0.8272 82.72%
CYP3A4 inhibition - 0.8512 85.12%
CYP2C9 inhibition - 0.9319 93.19%
CYP2C19 inhibition - 0.9267 92.67%
CYP2D6 inhibition - 0.9139 91.39%
CYP1A2 inhibition + 0.5395 53.95%
CYP2C8 inhibition - 0.6090 60.90%
CYP inhibitory promiscuity - 0.9415 94.15%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6833 68.33%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.8487 84.87%
Skin irritation - 0.7354 73.54%
Skin corrosion - 0.9092 90.92%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5248 52.48%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8437 84.37%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.5860 58.60%
Acute Oral Toxicity (c) III 0.6778 67.78%
Estrogen receptor binding + 0.7791 77.91%
Androgen receptor binding + 0.7567 75.67%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.8263 82.63%
Aromatase binding + 0.6867 68.67%
PPAR gamma + 0.8045 80.45%
Honey bee toxicity - 0.8927 89.27%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.8950 89.50%

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 99.73% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 98.34% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.72% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.69% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.42% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.33% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.94% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.60% 85.14%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.96% 93.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 89.61% 93.65%
CHEMBL1951 P21397 Monoamine oxidase A 88.94% 91.49%
CHEMBL5145 P15056 Serine/threonine-protein kinase B-raf 88.08% 97.90%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.28% 86.33%
CHEMBL4581 P52732 Kinesin-like protein 1 86.63% 93.18%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.78% 96.67%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.68% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.09% 94.00%
CHEMBL2535 P11166 Glucose transporter 84.42% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 83.79% 93.31%

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 10093690
LOTUS LTS0212038
wikiData Q77514868