5,7-Dihydroxy-2-(hydroxymethyl)-4H-1-benzopyran-4-one

Details

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Internal ID 37971079-3792-4277-93cc-11e82261e37a
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5,7-dihydroxy-2-(hydroxymethyl)chromen-4-one
SMILES (Canonical) C1=C(C=C2C(=C1O)C(=O)C=C(O2)CO)O
SMILES (Isomeric) C1=C(C=C2C(=C1O)C(=O)C=C(O2)CO)O
InChI InChI=1S/C10H8O5/c11-4-6-3-8(14)10-7(13)1-5(12)2-9(10)15-6/h1-3,11-13H,4H2
InChI Key YFSVMSTWCJUXNI-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8O5
Molecular Weight 208.17 g/mol
Exact Mass 208.03717335 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP -0.40
Atomic LogP (AlogP) 0.70
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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5,7-Dihydroxy-2-(hydroxymethyl)-4H-1-benzopyran-4-one
CHEMBL2087914
5,7-dihydroxy-2-hydroxymethylchromone
FT-0740424

2D Structure

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2D Structure of 5,7-Dihydroxy-2-(hydroxymethyl)-4H-1-benzopyran-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 + 0.9126 91.26%
Caco-2 + 0.6612 66.12%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5478 54.78%
OATP2B1 inhibitior - 0.7101 71.01%
OATP1B1 inhibitior + 0.9199 91.99%
OATP1B3 inhibitior + 0.9082 90.82%
MATE1 inhibitior + 0.5200 52.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9419 94.19%
P-glycoprotein inhibitior - 0.9535 95.35%
P-glycoprotein substrate - 0.9340 93.40%
CYP3A4 substrate - 0.6247 62.47%
CYP2C9 substrate - 0.6133 61.33%
CYP2D6 substrate - 0.8468 84.68%
CYP3A4 inhibition - 0.5188 51.88%
CYP2C9 inhibition - 0.7905 79.05%
CYP2C19 inhibition - 0.7823 78.23%
CYP2D6 inhibition - 0.9108 91.08%
CYP1A2 inhibition - 0.5108 51.08%
CYP2C8 inhibition - 0.7988 79.88%
CYP inhibitory promiscuity - 0.5090 50.90%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6451 64.51%
Eye corrosion - 0.9838 98.38%
Eye irritation + 0.9654 96.54%
Skin irritation - 0.6906 69.06%
Skin corrosion - 0.9694 96.94%
Ames mutagenesis + 0.6563 65.63%
Human Ether-a-go-go-Related Gene inhibition - 0.9023 90.23%
Micronuclear + 0.5359 53.59%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8204 82.04%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.6669 66.69%
Acute Oral Toxicity (c) II 0.4379 43.79%
Estrogen receptor binding + 0.6124 61.24%
Androgen receptor binding + 0.7386 73.86%
Thyroid receptor binding - 0.6219 62.19%
Glucocorticoid receptor binding + 0.7969 79.69%
Aromatase binding + 0.5684 56.84%
PPAR gamma + 0.7860 78.60%
Honey bee toxicity - 0.9139 91.39%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.6107 61.07%

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 98.33% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.15% 93.99%
CHEMBL3194 P02766 Transthyretin 92.38% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.90% 89.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 89.13% 96.12%
CHEMBL2581 P07339 Cathepsin D 87.57% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.41% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.82% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.35% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.91% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.12% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.05% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.66% 99.15%

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.
Cnidium monnieri
Torilis japonica

Cross-Links

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PubChem 70697378
NPASS NPC296380
LOTUS LTS0035517
wikiData Q105347788