2-Hydroxy-1-(5-hydroxy-2,2-dimethylchromen-6-yl)ethanone

Details

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Internal ID 3769d260-5c71-45d0-97e7-e8912178d6b5
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 2-hydroxy-1-(5-hydroxy-2,2-dimethylchromen-6-yl)ethanone
SMILES (Canonical) CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)CO)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)CO)C
InChI InChI=1S/C13H14O4/c1-13(2)6-5-9-11(17-13)4-3-8(12(9)16)10(15)7-14/h3-6,14,16H,7H2,1-2H3
InChI Key KIOAAZWXERJXQO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O4
Molecular Weight 234.25 g/mol
Exact Mass 234.08920892 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.75
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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BDBM50430026

2D Structure

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2D Structure of 2-Hydroxy-1-(5-hydroxy-2,2-dimethylchromen-6-yl)ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9628 96.28%
Caco-2 + 0.7222 72.22%
Blood Brain Barrier - 0.5395 53.95%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7898 78.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8946 89.46%
OATP1B3 inhibitior + 0.9733 97.33%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5893 58.93%
P-glycoprotein inhibitior - 0.9564 95.64%
P-glycoprotein substrate - 0.8059 80.59%
CYP3A4 substrate - 0.5203 52.03%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8390 83.90%
CYP3A4 inhibition - 0.6646 66.46%
CYP2C9 inhibition + 0.5745 57.45%
CYP2C19 inhibition + 0.6202 62.02%
CYP2D6 inhibition - 0.7320 73.20%
CYP1A2 inhibition + 0.7540 75.40%
CYP2C8 inhibition - 0.7767 77.67%
CYP inhibitory promiscuity + 0.6350 63.50%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6432 64.32%
Eye corrosion - 0.9886 98.86%
Eye irritation + 0.8326 83.26%
Skin irritation - 0.7479 74.79%
Skin corrosion - 0.9194 91.94%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7664 76.64%
Micronuclear - 0.5541 55.41%
Hepatotoxicity - 0.5542 55.42%
skin sensitisation - 0.6899 68.99%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5767 57.67%
Acute Oral Toxicity (c) III 0.5100 51.00%
Estrogen receptor binding + 0.8148 81.48%
Androgen receptor binding - 0.5883 58.83%
Thyroid receptor binding - 0.5332 53.32%
Glucocorticoid receptor binding + 0.8098 80.98%
Aromatase binding + 0.6283 62.83%
PPAR gamma + 0.7235 72.35%
Honey bee toxicity - 0.9585 95.85%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.8128 81.28%

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 97.80% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.70% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.67% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.19% 98.95%
CHEMBL4208 P20618 Proteasome component C5 86.77% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.05% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.64% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 84.44% 94.73%

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.
Brickellia cavanillesii

Cross-Links

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PubChem 59051355
LOTUS LTS0020342
wikiData Q103815862