Capillarisin

Details

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Internal ID bc78189f-faaf-4147-8931-7cf73607ff49
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 5,7-dihydroxy-2-(4-hydroxyphenoxy)-6-methoxychromen-4-one
SMILES (Canonical) COC1=C(C2=C(C=C1O)OC(=CC2=O)OC3=CC=C(C=C3)O)O
SMILES (Isomeric) COC1=C(C2=C(C=C1O)OC(=CC2=O)OC3=CC=C(C=C3)O)O
InChI InChI=1S/C16H12O7/c1-21-16-11(19)6-12-14(15(16)20)10(18)7-13(23-12)22-9-4-2-8(17)3-5-9/h2-7,17,19-20H,1H3
InChI Key NTKNGUAZSFAKEE-UHFFFAOYSA-N
Popularity 34 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O7
Molecular Weight 316.26 g/mol
Exact Mass 316.05830272 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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56365-38-9
Capillarisine
5,7-dihydroxy-2-(4-hydroxyphenoxy)-6-methoxychromen-4-one
5,7-dihydroxy-2-(4-hydroxyphenoxy)-6-methoxy-4H-chromen-4-one
C08999
AC1NQYDG
X1106
CHEBI:3368
CHEMBL4475774
SCHEMBL13906076
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Capillarisin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8997 89.97%
Caco-2 + 0.6456 64.56%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5553 55.53%
OATP2B1 inhibitior + 0.5564 55.64%
OATP1B1 inhibitior + 0.8746 87.46%
OATP1B3 inhibitior + 0.9258 92.58%
MATE1 inhibitior + 0.5600 56.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7077 70.77%
P-glycoprotein inhibitior - 0.4918 49.18%
P-glycoprotein substrate - 0.9074 90.74%
CYP3A4 substrate + 0.5546 55.46%
CYP2C9 substrate - 0.6296 62.96%
CYP2D6 substrate - 0.8329 83.29%
CYP3A4 inhibition - 0.6340 63.40%
CYP2C9 inhibition - 0.8339 83.39%
CYP2C19 inhibition - 0.7303 73.03%
CYP2D6 inhibition - 0.8388 83.88%
CYP1A2 inhibition + 0.8398 83.98%
CYP2C8 inhibition + 0.5409 54.09%
CYP inhibitory promiscuity + 0.5473 54.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6032 60.32%
Eye corrosion - 0.9670 96.70%
Eye irritation + 0.8597 85.97%
Skin irritation - 0.5615 56.15%
Skin corrosion - 0.9453 94.53%
Ames mutagenesis - 0.5154 51.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6652 66.52%
Micronuclear + 0.9300 93.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.9119 91.19%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.5893 58.93%
Acute Oral Toxicity (c) III 0.7646 76.46%
Estrogen receptor binding + 0.9210 92.10%
Androgen receptor binding + 0.8648 86.48%
Thyroid receptor binding + 0.5857 58.57%
Glucocorticoid receptor binding + 0.8450 84.50%
Aromatase binding + 0.7539 75.39%
PPAR gamma + 0.7451 74.51%
Honey bee toxicity - 0.8465 84.65%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.8725 87.25%

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 99.11% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.73% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.50% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.37% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.73% 95.56%
CHEMBL3194 P02766 Transthyretin 91.37% 90.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.03% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.72% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.71% 99.17%
CHEMBL4208 P20618 Proteasome component C5 88.43% 90.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.83% 93.99%
CHEMBL2535 P11166 Glucose transporter 86.09% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.14% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 84.95% 94.73%
CHEMBL2581 P07339 Cathepsin D 84.36% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.69% 93.65%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.34% 94.42%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.89% 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.
Artemisia capillaris
Artemisia scoparia

Cross-Links

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PubChem 5281342
NPASS NPC206093
LOTUS LTS0211683
wikiData Q27106050