Capillarin

Details

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Internal ID 5a25def6-0e09-4d9d-b72a-f37d2b8c2225
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 3-but-2-ynylisochromen-1-one
SMILES (Canonical) CC#CCC1=CC2=CC=CC=C2C(=O)O1
SMILES (Isomeric) CC#CCC1=CC2=CC=CC=C2C(=O)O1
InChI InChI=1S/C13H10O2/c1-2-3-7-11-9-10-6-4-5-8-12(10)13(14)15-11/h4-6,8-9H,7H2,1H3
InChI Key KUJLPCYCQICVRM-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10O2
Molecular Weight 198.22 g/mol
Exact Mass 198.068079557 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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3570-28-3
3-but-2-ynylisochromen-1-one
G5ANW3JF5K
1H-2-Benzopyran-1-one, 3-(2-butynyl)-
3-(2-Butynyl)-1H-2-benzopyran-1-one
UNII-G5ANW3JF5K
3-(but-2-ynyl) isocoumarin
CHEBI:80801
MLS000863656
CHEMBL479330
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Capillarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.8015 80.15%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4991 49.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9099 90.99%
OATP1B3 inhibitior + 0.9692 96.92%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8313 83.13%
P-glycoprotein inhibitior - 0.9410 94.10%
P-glycoprotein substrate - 0.9245 92.45%
CYP3A4 substrate - 0.5629 56.29%
CYP2C9 substrate - 0.5872 58.72%
CYP2D6 substrate - 0.8584 85.84%
CYP3A4 inhibition - 0.7316 73.16%
CYP2C9 inhibition - 0.7962 79.62%
CYP2C19 inhibition - 0.6713 67.13%
CYP2D6 inhibition - 0.9419 94.19%
CYP1A2 inhibition + 0.8772 87.72%
CYP2C8 inhibition - 0.7848 78.48%
CYP inhibitory promiscuity - 0.6966 69.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8513 85.13%
Carcinogenicity (trinary) Non-required 0.4350 43.50%
Eye corrosion - 0.9095 90.95%
Eye irritation + 0.7128 71.28%
Skin irritation + 0.5877 58.77%
Skin corrosion - 0.9339 93.39%
Ames mutagenesis + 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7652 76.52%
Micronuclear - 0.6100 61.00%
Hepatotoxicity + 0.7574 75.74%
skin sensitisation - 0.6067 60.67%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6897 68.97%
Acute Oral Toxicity (c) III 0.7670 76.70%
Estrogen receptor binding - 0.5473 54.73%
Androgen receptor binding + 0.7052 70.52%
Thyroid receptor binding - 0.5753 57.53%
Glucocorticoid receptor binding - 0.5353 53.53%
Aromatase binding + 0.5739 57.39%
PPAR gamma - 0.5144 51.44%
Honey bee toxicity - 0.9389 93.89%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.8595 85.95%

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 98.02% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.35% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.27% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 92.25% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.31% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.51% 93.65%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.27% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.54% 95.50%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.18% 96.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.01% 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 dracunculus
Artemisia norvegica subsp. saxatilis
Artemisia scoparia
Artemisia scoparia
Seriphidium turanicum
Zanthoxylum nitidum

Cross-Links

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PubChem 3083811
NPASS NPC269023
ChEMBL CHEMBL479330
LOTUS LTS0037593
wikiData Q27149844