5-hydroxy-4H-chromen-4-one

Details

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Internal ID f46ba821-7264-40f5-9744-2b8350d4f304
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5-hydroxychromen-4-one
SMILES (Canonical) C1=CC(=C2C(=O)C=COC2=C1)O
SMILES (Isomeric) C1=CC(=C2C(=O)C=COC2=C1)O
InChI InChI=1S/C9H6O3/c10-6-2-1-3-8-9(6)7(11)4-5-12-8/h1-5,10H
InChI Key CJMXMDVAKVSKFI-UHFFFAOYSA-N
Popularity 36 references in papers

Physical and Chemical Properties

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Molecular Formula C9H6O3
Molecular Weight 162.14 g/mol
Exact Mass 162.031694049 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.50
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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3952-69-0
5-hydroxychromen-4-one
5-Hydroxy-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one,5-hydroxy-
MFCD00100605
5-hydroxychromone
5-hydroxy-chromen-4-one
orb3029937
SCHEMBL1857840
SCHEMBL11412674
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-hydroxy-4H-chromen-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 + 0.9955 99.55%
Caco-2 + 0.8820 88.20%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6018 60.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9599 95.99%
OATP1B3 inhibitior + 0.9938 99.38%
MATE1 inhibitior - 0.5200 52.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9493 94.93%
P-glycoprotein inhibitior - 0.9651 96.51%
P-glycoprotein substrate - 0.9793 97.93%
CYP3A4 substrate - 0.6430 64.30%
CYP2C9 substrate - 0.6265 62.65%
CYP2D6 substrate - 0.8495 84.95%
CYP3A4 inhibition - 0.6607 66.07%
CYP2C9 inhibition - 0.7608 76.08%
CYP2C19 inhibition + 0.6440 64.40%
CYP2D6 inhibition - 0.9207 92.07%
CYP1A2 inhibition + 0.9767 97.67%
CYP2C8 inhibition - 0.8869 88.69%
CYP inhibitory promiscuity - 0.7610 76.10%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.4615 46.15%
Eye corrosion - 0.9269 92.69%
Eye irritation + 0.9969 99.69%
Skin irritation + 0.7953 79.53%
Skin corrosion - 0.9929 99.29%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8920 89.20%
Micronuclear + 0.7759 77.59%
Hepatotoxicity + 0.7783 77.83%
skin sensitisation - 0.7677 76.77%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.6510 65.10%
Acute Oral Toxicity (c) III 0.6975 69.75%
Estrogen receptor binding - 0.6497 64.97%
Androgen receptor binding - 0.6074 60.74%
Thyroid receptor binding - 0.5626 56.26%
Glucocorticoid receptor binding - 0.7053 70.53%
Aromatase binding - 0.6543 65.43%
PPAR gamma + 0.5718 57.18%
Honey bee toxicity - 0.9438 94.38%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.7626 76.26%

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 97.01% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 94.84% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.19% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.68% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.86% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.39% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 87.07% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.28% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.40% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.79% 94.45%

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.
Persicaria capitata

Cross-Links

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PubChem 5479462
LOTUS LTS0176832
wikiData Q82231772