Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C15H20O2 |
Molecular Weight | 232.3181 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12C[C@@]3(C)CCC[C@H](C)C3=C[C@]1([H])C(=C)C(=O)O2
InChI
InChIKey=PXOYOCNNSUAQNS-AGNJHWRGSA-N
InChI=1S/C15H20O2/c1-9-5-4-6-15(3)8-13-11(7-12(9)15)10(2)14(16)17-13/h7,9,11,13H,2,4-6,8H2,1,3H3/t9-,11+,13+,15+/m0/s1
Molecular Formula | C15H20O2 |
Molecular Weight | 232.3181 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/24288468Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/22837216
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24288468
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/22837216
Alantolactone and isoalantolactone, main bioactive compounds that are present in many medicinal plants such as Inula helenium, L. Inula japonica, Aucklandia lappa, Inula racemosa, and Radix inulae, have been found to have various pharmacological actions including anti-inflammatory, antimicrobial, and anticancer properties, with no significant toxicity. Alantolactone and isoalantolactone have been reported for their wide spectrum of biological effects, including antifungal, anthelmintic activities, antimicrobial activities, anti-inflammatory activities, antitrypanosomal activities, and antiproliferative effects on several cancer cell lines, such as colon, melanoma, ovary, prostate, lung, and leukemia. Alantolactone isolated from Inula helenium (Compositae), a traditional Chinese medicinal herb, provides an effective inhibitory activity for cell growth against MK-1, HeLa, B16F10, and K562 cell lines. Many other human cancer cell lines, including U87 glioma cells, Bel-742, SMMC-7721 and HepG2 liver cancer cells, PANC-1 pancreatic carcinoma cells, A59 lung cancer cells, colon adenocarcinoma HCT-8 cells, CNS cancer cell line SF-295, leukemia HL-60, Hepa1c1c7 cells, BPRc1 Hepatic cancer cells, and HCT-8 colon cancer cells, have also been reported for apoptosis caused by alantolactone.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22837216
Curator's Comment: Alantolactone can cross blood–brain barrier.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL385 |
4.7 µM [IC50] | ||
Target ID: CHEMBL614247 |
33.0 µM [IC50] | ||
Target ID: CHEMBL614882 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26524033 |
4.32 µM [IC50] | ||
Target ID: CHEMBL340 Sources: https://www.ncbi.nlm.nih.gov/pubmed/25858508 |
3.9 µM [IC50] | ||
Target ID: CHEMBL377 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26781801 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
Antimycobacterial plant terpenoids. | 2001 Nov |
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Induction of detoxifying enzyme by sesquiterpenes present in Inula helenium. | 2007 Sep |
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Isoalantolactone from Inula helenium caused Nrf2-mediated induction of detoxifying enzymes. | 2009 Oct |
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Protective effect of stem bark of Ceiba pentandra linn. against paracetamol-induced hepatotoxicity in rats. | 2010 Jan |
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Structure-activity relationship studies on derivatives of eudesmanolides from Inula helenium as toxicants against Aedes aegypti larvae and adults. | 2010 Jul |
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Alantolactone induces activation of apoptosis in human hepatoma cells. | 2012 Sep |
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Alantolactone induces cell apoptosis partially through down-regulation of testes-specific protease 50 expression. | 2014 Jan 30 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22837216
Mice: alantolactone (100 mg/kg body weight) in 100 uL DMSO intraperitoneally
Route of Administration:
Intraperitoneal
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24985175
Alantolactone could effectively inhibit the proliferation of K562/ADR cells in dose- and time- dependent manner, the IC50 value of alantolactone treatment of K562/ADR cells for 24 h was 4.7 umol/L
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:35:59 GMT 2023
by
admin
on
Fri Dec 15 18:35:59 GMT 2023
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Record UNII |
M7GSN5Q1M6
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Record Status |
Validated (UNII)
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Record Version |
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