5-Hydroxy-2-hydroxymethyl-4h-chromen-4-one

Details

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Internal ID 6aca858c-66ef-465d-9e5d-3b4506a6566f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5-hydroxy-2-(hydroxymethyl)chromen-4-one
SMILES (Canonical) C1=CC(=C2C(=C1)OC(=CC2=O)CO)O
SMILES (Isomeric) C1=CC(=C2C(=C1)OC(=CC2=O)CO)O
InChI InChI=1S/C10H8O4/c11-5-6-4-8(13)10-7(12)2-1-3-9(10)14-6/h1-4,11-12H,5H2
InChI Key ITSDTMBVFOEMOC-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H8O4
Molecular Weight 192.17 g/mol
Exact Mass 192.04225873 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.99
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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2-(Hydroxymethyl)-5-hydroxy-4H-1-benzopyran-4-one

2D Structure

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2D Structure of 5-Hydroxy-2-hydroxymethyl-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 + 0.9637 96.37%
Caco-2 + 0.5581 55.81%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6742 67.42%
OATP2B1 inhibitior - 0.8614 86.14%
OATP1B1 inhibitior + 0.9402 94.02%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior + 0.5200 52.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9387 93.87%
P-glycoprotein inhibitior - 0.9686 96.86%
P-glycoprotein substrate - 0.9406 94.06%
CYP3A4 substrate - 0.6465 64.65%
CYP2C9 substrate - 0.6133 61.33%
CYP2D6 substrate - 0.8468 84.68%
CYP3A4 inhibition - 0.7614 76.14%
CYP2C9 inhibition - 0.7247 72.47%
CYP2C19 inhibition - 0.7291 72.91%
CYP2D6 inhibition - 0.9086 90.86%
CYP1A2 inhibition + 0.6065 60.65%
CYP2C8 inhibition - 0.8972 89.72%
CYP inhibitory promiscuity - 0.5856 58.56%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5792 57.92%
Eye corrosion - 0.9790 97.90%
Eye irritation + 0.9707 97.07%
Skin irritation - 0.6860 68.60%
Skin corrosion - 0.9765 97.65%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9049 90.49%
Micronuclear + 0.5459 54.59%
Hepatotoxicity - 0.5967 59.67%
skin sensitisation - 0.8371 83.71%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6312 63.12%
Acute Oral Toxicity (c) II 0.5398 53.98%
Estrogen receptor binding + 0.5484 54.84%
Androgen receptor binding + 0.6465 64.65%
Thyroid receptor binding - 0.5840 58.40%
Glucocorticoid receptor binding + 0.6482 64.82%
Aromatase binding + 0.5693 56.93%
PPAR gamma + 0.8554 85.54%
Honey bee toxicity - 0.9569 95.69%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.5562 55.62%

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 98.04% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.15% 93.99%
CHEMBL2581 P07339 Cathepsin D 93.28% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.69% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 90.71% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.44% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.93% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.03% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.51% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.76% 94.45%
CHEMBL3194 P02766 Transthyretin 81.23% 90.71%

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.
Acacia confusa
Erica arborea
Erica arborea
Isodon lihsienensis
Phoebe clemensii

Cross-Links

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PubChem 42604935
NPASS NPC21458
LOTUS LTS0240569
wikiData Q77280619