3,7-Dihydroxychromen-4-one

Details

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Internal ID fc2b9b88-1d03-4415-8318-43cb51757662
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 3,7-dihydroxychromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H6O4/c10-5-1-2-6-8(3-5)13-4-7(11)9(6)12/h1-4,10-11H
InChI Key ZZYLCDXPJISRAD-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C9H6O4
Molecular Weight 178.14 g/mol
Exact Mass 178.02660867 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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CHEMBL1916189
SCHEMBL11412845
CHEBI:69203
3,7-dihydroxy-4h-chromen-4-one
Q27137542

2D Structure

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2D Structure of 3,7-Dihydroxychromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9698 96.98%
Caco-2 + 0.6475 64.75%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7245 72.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9374 93.74%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9389 93.89%
P-glycoprotein inhibitior - 0.9664 96.64%
P-glycoprotein substrate - 0.9413 94.13%
CYP3A4 substrate - 0.6132 61.32%
CYP2C9 substrate - 0.8238 82.38%
CYP2D6 substrate - 0.8051 80.51%
CYP3A4 inhibition - 0.7696 76.96%
CYP2C9 inhibition + 0.8212 82.12%
CYP2C19 inhibition + 0.5862 58.62%
CYP2D6 inhibition - 0.8804 88.04%
CYP1A2 inhibition + 0.9641 96.41%
CYP2C8 inhibition - 0.7829 78.29%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6103 61.03%
Eye corrosion - 0.9827 98.27%
Eye irritation + 0.9970 99.70%
Skin irritation + 0.7243 72.43%
Skin corrosion - 0.9784 97.84%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9057 90.57%
Micronuclear + 0.9500 95.00%
Hepatotoxicity + 0.6783 67.83%
skin sensitisation - 0.7121 71.21%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.4882 48.82%
Acute Oral Toxicity (c) II 0.4540 45.40%
Estrogen receptor binding - 0.5961 59.61%
Androgen receptor binding + 0.7934 79.34%
Thyroid receptor binding - 0.5405 54.05%
Glucocorticoid receptor binding - 0.5709 57.09%
Aromatase binding - 0.5389 53.89%
PPAR gamma - 0.4924 49.24%
Honey bee toxicity - 0.9132 91.32%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8938 89.38%

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 98.61% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.12% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.65% 89.00%
CHEMBL3194 P02766 Transthyretin 87.83% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.77% 94.45%
CHEMBL2581 P07339 Cathepsin D 87.66% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.98% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.01% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 80.25% 94.73%

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.
Biancaea sappan

Cross-Links

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PubChem 57401583
NPASS NPC291684
LOTUS LTS0050850
wikiData Q27137542