Capillartemisin A

Details

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Internal ID cf094ce1-8054-4f3b-908f-6d432f6db4ad
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acids
IUPAC Name (E)-3-[4-hydroxy-3-[(E)-4-hydroxy-3-methylbut-2-enyl]-5-(3-methylbut-2-enyl)phenyl]prop-2-enoic acid
SMILES (Canonical) CC(=CCC1=C(C(=CC(=C1)C=CC(=O)O)CC=C(C)CO)O)C
SMILES (Isomeric) CC(=CCC1=C(C(=CC(=C1)/C=C/C(=O)O)C/C=C(\C)/CO)O)C
InChI InChI=1S/C19H24O4/c1-13(2)4-7-16-10-15(6-9-18(21)22)11-17(19(16)23)8-5-14(3)12-20/h4-6,9-11,20,23H,7-8,12H2,1-3H3,(H,21,22)/b9-6+,14-5+
InChI Key HEFPIIHDRLNTDN-JBFPSKHUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O4
Molecular Weight 316.40 g/mol
Exact Mass 316.16745924 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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85819-52-9
(E)-3-[4-hydroxy-3-[(E)-4-hydroxy-3-methylbut-2-enyl]-5-(3-methylbut-2-enyl)phenyl]prop-2-enoic acid
CHEMBL4855416
SCHEMBL23742688
CHEBI:81341
DTXSID101316451
C17789
Q27155278
2-Propenoic acid, 3-(4-hydroxy-3-(4-hydroxy-3-methyl-2-butenyl)-5-(3-methyl-2-butenyl)phenyl)-, (E,E)-

2D Structure

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2D Structure of Capillartemisin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.9183 91.83%
OATP2B1 inhibitior - 0.5671 56.71%
OATP1B1 inhibitior + 0.8619 86.19%
OATP1B3 inhibitior + 0.9156 91.56%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8427 84.27%
P-glycoprotein inhibitior - 0.8328 83.28%
P-glycoprotein substrate - 0.8643 86.43%
CYP3A4 substrate - 0.5792 57.92%
CYP2C9 substrate - 0.5996 59.96%
CYP2D6 substrate - 0.8693 86.93%
CYP3A4 inhibition + 0.6433 64.33%
CYP2C9 inhibition - 0.5169 51.69%
CYP2C19 inhibition + 0.5918 59.18%
CYP2D6 inhibition - 0.7336 73.36%
CYP1A2 inhibition + 0.7575 75.75%
CYP2C8 inhibition - 0.7788 77.88%
CYP inhibitory promiscuity - 0.5445 54.45%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6870 68.70%
Carcinogenicity (trinary) Non-required 0.7413 74.13%
Eye corrosion - 0.9869 98.69%
Eye irritation + 0.6386 63.86%
Skin irritation - 0.7928 79.28%
Skin corrosion - 0.9574 95.74%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5604 56.04%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.7593 75.93%
skin sensitisation - 0.5664 56.64%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6752 67.52%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.6723 67.23%
Acute Oral Toxicity (c) III 0.5050 50.50%
Estrogen receptor binding + 0.7228 72.28%
Androgen receptor binding + 0.7444 74.44%
Thyroid receptor binding + 0.6139 61.39%
Glucocorticoid receptor binding + 0.8048 80.48%
Aromatase binding + 0.6212 62.12%
PPAR gamma + 0.8352 83.52%
Honey bee toxicity - 0.9440 94.40%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 1.0000 100.00%

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 97.79% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.74% 91.49%
CHEMBL2581 P07339 Cathepsin D 92.16% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.63% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.49% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 89.69% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.25% 91.71%
CHEMBL221 P23219 Cyclooxygenase-1 86.83% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.58% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.24% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.88% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.35% 89.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.70% 89.34%

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 palustris

Cross-Links

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PubChem 6439717
NPASS NPC302890
LOTUS LTS0265142
wikiData Q27155278