Bisanhydro-Gamma-Rhodomycinone

Details

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Internal ID ec6ad7a1-a284-4896-8775-150903f567cc
Taxonomy Benzenoids > Naphthacenes > Tetracenequinones
IUPAC Name 8-ethyl-1,6,11-trihydroxytetracene-5,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H14O5/c1-2-9-6-7-10-12(8-9)19(24)15-16(17(10)22)20(25)14-11(18(15)23)4-3-5-13(14)21/h3-8,21-22,24H,2H2,1H3
InChI Key IQQXEUJGABFGFT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H14O5
Molecular Weight 334.30 g/mol
Exact Mass 334.08412354 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 5.00
Atomic LogP (AlogP) 3.29
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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5236-40-8
SCHEMBL17867127
DTXSID90631685

2D Structure

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2D Structure of Bisanhydro-Gamma-Rhodomycinone

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 - 0.5502 55.02%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8650 86.50%
OATP2B1 inhibitior - 0.5576 55.76%
OATP1B1 inhibitior + 0.9015 90.15%
OATP1B3 inhibitior + 0.9591 95.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.5725 57.25%
P-glycoprotein inhibitior - 0.8202 82.02%
P-glycoprotein substrate - 0.6664 66.64%
CYP3A4 substrate + 0.5134 51.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7875 78.75%
CYP3A4 inhibition - 0.8479 84.79%
CYP2C9 inhibition + 0.8559 85.59%
CYP2C19 inhibition + 0.5668 56.68%
CYP2D6 inhibition - 0.7397 73.97%
CYP1A2 inhibition + 0.8547 85.47%
CYP2C8 inhibition - 0.6609 66.09%
CYP inhibitory promiscuity - 0.5561 55.61%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7409 74.09%
Carcinogenicity (trinary) Non-required 0.5249 52.49%
Eye corrosion - 0.9874 98.74%
Eye irritation + 0.7171 71.71%
Skin irritation - 0.5378 53.78%
Skin corrosion - 0.9389 93.89%
Ames mutagenesis + 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7135 71.35%
Micronuclear + 0.7059 70.59%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.8295 82.95%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7637 76.37%
Acute Oral Toxicity (c) II 0.6251 62.51%
Estrogen receptor binding + 0.8036 80.36%
Androgen receptor binding + 0.7916 79.16%
Thyroid receptor binding - 0.5568 55.68%
Glucocorticoid receptor binding + 0.9085 90.85%
Aromatase binding + 0.5492 54.92%
PPAR gamma + 0.8958 89.58%
Honey bee toxicity - 0.9047 90.47%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9859 98.59%

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 99.54% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 99.43% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.54% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.81% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.53% 89.00%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 89.53% 92.67%
CHEMBL3401 O75469 Pregnane X receptor 88.77% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.13% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.04% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.60% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.23% 96.95%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.31% 96.67%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 82.49% 96.37%
CHEMBL2535 P11166 Glucose transporter 81.54% 98.75%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.18% 93.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.98% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.79% 95.50%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.51% 99.15%

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 23260551
LOTUS LTS0178178
wikiData Q82538964