Flaviolin

Details

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Internal ID 0cab3a09-97f4-42d0-abc9-2a7ba9eee8b1
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 4,5,7-trihydroxynaphthalene-1,2-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H6O5/c11-4-1-5-9(6(12)2-4)7(13)3-8(14)10(5)15/h1-3,11-13H
InChI Key XNPCAGMCQDGQKK-UHFFFAOYSA-N
Popularity 144 references in papers

Physical and Chemical Properties

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Molecular Formula C10H6O5
Molecular Weight 206.15 g/mol
Exact Mass 206.02152329 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.76
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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4,5,7-trihydroxynaphthalene-1,2-dione
479-05-0
2,5,7-TRIHYDROXYNAPHTHOQUINONE
2,5,7-Trihydroxy-1,4-naphthalenedione
1,4-Naphthalenedione, 2,5,7-trihydroxy-
TH7ZC8J7OE
2,5,7-trihydroxynaphthalene-1,4-dione
CHEBI:42646
2,5,7-trihydroxy-1,4-naphthoquinone
UNII-TH7ZC8J7OE
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Flaviolin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9866 98.66%
Caco-2 + 0.5519 55.19%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5904 59.04%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.9271 92.71%
OATP1B3 inhibitior + 0.9288 92.88%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9838 98.38%
BSEP inhibitior - 0.9870 98.70%
P-glycoprotein inhibitior - 0.9698 96.98%
P-glycoprotein substrate - 0.9618 96.18%
CYP3A4 substrate - 0.5941 59.41%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8536 85.36%
CYP3A4 inhibition - 0.6407 64.07%
CYP2C9 inhibition + 0.8901 89.01%
CYP2C19 inhibition - 0.6639 66.39%
CYP2D6 inhibition - 0.8411 84.11%
CYP1A2 inhibition + 0.7881 78.81%
CYP2C8 inhibition - 0.8876 88.76%
CYP inhibitory promiscuity + 0.7289 72.89%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9092 90.92%
Carcinogenicity (trinary) Non-required 0.5378 53.78%
Eye corrosion - 0.9801 98.01%
Eye irritation + 0.9956 99.56%
Skin irritation + 0.7634 76.34%
Skin corrosion - 0.8906 89.06%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8688 86.88%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.6731 67.31%
skin sensitisation + 0.7698 76.98%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.7407 74.07%
Acute Oral Toxicity (c) III 0.4440 44.40%
Estrogen receptor binding - 0.5857 58.57%
Androgen receptor binding + 0.5339 53.39%
Thyroid receptor binding - 0.6914 69.14%
Glucocorticoid receptor binding + 0.6979 69.79%
Aromatase binding - 0.6723 67.23%
PPAR gamma - 0.6228 62.28%
Honey bee toxicity - 0.8669 86.69%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9860 98.60%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.81% 91.11%
CHEMBL1929 P47989 Xanthine dehydrogenase 93.01% 96.12%
CHEMBL2581 P07339 Cathepsin D 92.78% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.92% 93.40%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.74% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.33% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 86.32% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.65% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.01% 99.23%
CHEMBL3194 P02766 Transthyretin 83.67% 90.71%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.42% 96.67%
CHEMBL4208 P20618 Proteasome component C5 82.15% 90.00%
CHEMBL1937 Q92769 Histone deacetylase 2 80.92% 94.75%

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.
Artemisia annua
Artemisia carvifolia

Cross-Links

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PubChem 160478
NPASS NPC252101
LOTUS LTS0027516
wikiData Q104395374