(2R)-2,5-dihydroxy-7-methoxy-2-methyl-3H-chromen-4-one

Details

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Internal ID 65f31ab1-2bf6-448f-b05a-7ade20d67df0
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name (2R)-2,5-dihydroxy-7-methoxy-2-methyl-3H-chromen-4-one
SMILES (Canonical) CC1(CC(=O)C2=C(C=C(C=C2O1)OC)O)O
SMILES (Isomeric) C[C@@]1(CC(=O)C2=C(C=C(C=C2O1)OC)O)O
InChI InChI=1S/C11H12O5/c1-11(14)5-8(13)10-7(12)3-6(15-2)4-9(10)16-11/h3-4,12,14H,5H2,1-2H3/t11-/m1/s1
InChI Key ZZCQGUGZJOVBQE-LLVKDONJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O5
Molecular Weight 224.21 g/mol
Exact Mass 224.06847348 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.07
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2,5-dihydroxy-7-methoxy-2-methyl-3H-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 + 0.9271 92.71%
Caco-2 + 0.8539 85.39%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6738 67.38%
OATP2B1 inhibitior - 0.8608 86.08%
OATP1B1 inhibitior + 0.9251 92.51%
OATP1B3 inhibitior + 0.9665 96.65%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8978 89.78%
P-glycoprotein inhibitior - 0.9489 94.89%
P-glycoprotein substrate - 0.9583 95.83%
CYP3A4 substrate + 0.5246 52.46%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8045 80.45%
CYP3A4 inhibition - 0.7525 75.25%
CYP2C9 inhibition - 0.7820 78.20%
CYP2C19 inhibition - 0.7676 76.76%
CYP2D6 inhibition - 0.6823 68.23%
CYP1A2 inhibition + 0.6300 63.00%
CYP2C8 inhibition - 0.7933 79.33%
CYP inhibitory promiscuity - 0.8373 83.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.5735 57.35%
Eye corrosion - 0.9753 97.53%
Eye irritation + 0.8579 85.79%
Skin irritation - 0.7094 70.94%
Skin corrosion - 0.9480 94.80%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7532 75.32%
Micronuclear + 0.6300 63.00%
Hepatotoxicity - 0.6967 69.67%
skin sensitisation - 0.8895 88.95%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.7732 77.32%
Acute Oral Toxicity (c) III 0.4211 42.11%
Estrogen receptor binding + 0.6269 62.69%
Androgen receptor binding - 0.5185 51.85%
Thyroid receptor binding - 0.5895 58.95%
Glucocorticoid receptor binding - 0.5321 53.21%
Aromatase binding + 0.5950 59.50%
PPAR gamma + 0.6647 66.47%
Honey bee toxicity - 0.8848 88.48%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.7445 74.45%

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 99.09% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.43% 94.45%
CHEMBL4208 P20618 Proteasome component C5 95.01% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.38% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.26% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.81% 99.15%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.05% 91.07%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.06% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.58% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.22% 94.00%
CHEMBL2581 P07339 Cathepsin D 88.53% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.18% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.56% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.45% 92.94%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 84.74% 92.68%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.24% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.67% 86.33%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 81.61% 80.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.25% 89.00%

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.
Hymenophyton flabellatum

Cross-Links

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PubChem 163027051
LOTUS LTS0063922
wikiData Q105386678