5-Hydroxy-7-methoxycoumarin

Details

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Internal ID 407097b4-2472-401b-904f-c7e3bcdf142a
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins
IUPAC Name 5-hydroxy-7-methoxychromen-2-one
SMILES (Canonical) COC1=CC(=C2C=CC(=O)OC2=C1)O
SMILES (Isomeric) COC1=CC(=C2C=CC(=O)OC2=C1)O
InChI InChI=1S/C10H8O4/c1-13-6-4-8(11)7-2-3-10(12)14-9(7)5-6/h2-5,11H,1H3
InChI Key CPPAWCQANCLZEO-UHFFFAOYSA-N
Popularity 12 references 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) 55.80 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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23053-61-4
5-hydroxy-7-methoxy-2H-chromen-2-one
DTXSID20177622
5-Hydroxy-7-methoxy-2H-1-benzopyran-2-one

2D Structure

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2D Structure of 5-Hydroxy-7-methoxycoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9835 98.35%
Caco-2 + 0.8241 82.41%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6248 62.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.9922 99.22%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8658 86.58%
P-glycoprotein inhibitior - 0.8851 88.51%
P-glycoprotein substrate - 0.9480 94.80%
CYP3A4 substrate - 0.5984 59.84%
CYP2C9 substrate - 0.8431 84.31%
CYP2D6 substrate - 0.8139 81.39%
CYP3A4 inhibition - 0.5830 58.30%
CYP2C9 inhibition - 0.6816 68.16%
CYP2C19 inhibition - 0.6998 69.98%
CYP2D6 inhibition - 0.9181 91.81%
CYP1A2 inhibition + 0.9369 93.69%
CYP2C8 inhibition - 0.7727 77.27%
CYP inhibitory promiscuity - 0.7413 74.13%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.4500 45.00%
Eye corrosion - 0.8752 87.52%
Eye irritation + 0.9848 98.48%
Skin irritation - 0.5604 56.04%
Skin corrosion - 0.9866 98.66%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8500 85.00%
Micronuclear + 0.8800 88.00%
Hepatotoxicity - 0.6300 63.00%
skin sensitisation - 0.9660 96.60%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.6200 62.00%
Acute Oral Toxicity (c) III 0.8543 85.43%
Estrogen receptor binding + 0.7393 73.93%
Androgen receptor binding + 0.8675 86.75%
Thyroid receptor binding - 0.7202 72.02%
Glucocorticoid receptor binding + 0.7153 71.53%
Aromatase binding + 0.8138 81.38%
PPAR gamma + 0.6247 62.47%
Honey bee toxicity - 0.9323 93.23%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8192 81.92%

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 98.86% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.96% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.08% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.98% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.96% 94.00%
CHEMBL2581 P07339 Cathepsin D 90.35% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.55% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.40% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 84.11% 91.49%
CHEMBL2535 P11166 Glucose transporter 83.45% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.65% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 82.42% 94.73%
CHEMBL4208 P20618 Proteasome component C5 82.01% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.05% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.61% 85.14%

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.
Haplophyllum bungei
Lobelia chinensis
Morus alba

Cross-Links

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PubChem 5748603
NPASS NPC3665
LOTUS LTS0183894
wikiData Q72484782