Saikochromone A

Details

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Internal ID e7a46520-4bc1-4d9e-b02f-4779a6e78b29
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5-hydroxy-2-(hydroxymethyl)-7-methoxychromen-4-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC(=CC2=O)CO)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC(=CC2=O)CO)O
InChI InChI=1S/C11H10O5/c1-15-6-2-8(13)11-9(14)3-7(5-12)16-10(11)4-6/h2-4,12-13H,5H2,1H3
InChI Key LDNAYBDXSSEORD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O5
Molecular Weight 222.19 g/mol
Exact Mass 222.05282342 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 1.00
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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SCHEMBL14252989
AKOS040763364
132624-99-8

2D Structure

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2D Structure of Saikochromone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9627 96.27%
Caco-2 + 0.6952 69.52%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7260 72.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9243 92.43%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.6200 62.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8839 88.39%
P-glycoprotein inhibitior - 0.9048 90.48%
P-glycoprotein substrate - 0.9164 91.64%
CYP3A4 substrate - 0.5674 56.74%
CYP2C9 substrate - 0.6235 62.35%
CYP2D6 substrate - 0.8293 82.93%
CYP3A4 inhibition - 0.6907 69.07%
CYP2C9 inhibition - 0.6225 62.25%
CYP2C19 inhibition + 0.5222 52.22%
CYP2D6 inhibition - 0.8537 85.37%
CYP1A2 inhibition + 0.6402 64.02%
CYP2C8 inhibition - 0.8064 80.64%
CYP inhibitory promiscuity + 0.5626 56.26%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5922 59.22%
Eye corrosion - 0.9600 96.00%
Eye irritation + 0.8832 88.32%
Skin irritation - 0.7864 78.64%
Skin corrosion - 0.9788 97.88%
Ames mutagenesis + 0.6463 64.63%
Human Ether-a-go-go-Related Gene inhibition - 0.9079 90.79%
Micronuclear + 0.5959 59.59%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8932 89.32%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7031 70.31%
Acute Oral Toxicity (c) III 0.8041 80.41%
Estrogen receptor binding + 0.7317 73.17%
Androgen receptor binding + 0.7528 75.28%
Thyroid receptor binding - 0.6152 61.52%
Glucocorticoid receptor binding + 0.7448 74.48%
Aromatase binding + 0.7116 71.16%
PPAR gamma + 0.7365 73.65%
Honey bee toxicity - 0.9184 91.84%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.6856 68.56%

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 98.58% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.46% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.16% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.80% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.95% 99.15%
CHEMBL2581 P07339 Cathepsin D 89.08% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.66% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.26% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 87.89% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.53% 94.45%
CHEMBL3194 P02766 Transthyretin 85.10% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.02% 86.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.76% 86.92%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.62% 89.00%
CHEMBL4208 P20618 Proteasome component C5 82.33% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.03% 96.09%

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.
Bupleurum falcatum
Bupleurum scorzonerifolium
Harrisonia perforata

Cross-Links

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PubChem 10013795
NPASS NPC174118
LOTUS LTS0209207
wikiData Q105269697