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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
Structure of ALANTOLACTONE

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

HIDE SMILES / InChI

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

Description
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

Curator's Comment: Alantolactone can cross blood–brain barrier.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Antimycobacterial plant terpenoids.
2001 Nov
Induction of detoxifying enzyme by sesquiterpenes present in Inula helenium.
2007 Sep
Isoalantolactone from Inula helenium caused Nrf2-mediated induction of detoxifying enzymes.
2009 Oct
Protective effect of stem bark of Ceiba pentandra linn. against paracetamol-induced hepatotoxicity in rats.
2010 Jan
Structure-activity relationship studies on derivatives of eudesmanolides from Inula helenium as toxicants against Aedes aegypti larvae and adults.
2010 Jul
Alantolactone induces activation of apoptosis in human hepatoma cells.
2012 Sep
Alantolactone induces cell apoptosis partially through down-regulation of testes-specific protease 50 expression.
2014 Jan 30
Patents

Sample Use Guides

Mice: alantolactone (100 mg/kg body weight) in 100 uL DMSO intraperitoneally
Route of Administration: Intraperitoneal
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 Fri Dec 15 18:35:59 GMT 2023
Edited
by admin
on Fri Dec 15 18:35:59 GMT 2023
Record UNII
M7GSN5Q1M6
Record Status Validated (UNII)
Record Version
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Name Type Language
ALANTOLACTONE
MI  
Common Name English
NSC-333843
Code English
ALANTOLACTONE [MI]
Common Name English
INULA CAMPHOR
Common Name English
NSC-93131
Code English
ALANT CAMPHOR
Common Name English
ELECAMPANE CAMPHOR
Common Name English
HELENIN
Common Name English
8.BETA.-HYDROXY-4.ALPHA.H-EUDESM-5-EN-12-OIC ACID .GAMMA.-LACTONE
Common Name English
Code System Code Type Description
NSC
333843
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-899-3
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
PRIMARY
MERCK INDEX
m1470
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
Alantolactone
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
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PUBCHEM
72724
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
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CHEBI
2540
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
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NSC
93131
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
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CAS
546-43-0
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
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EVMPD
SUB169777
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
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EPA CompTox
DTXSID90877864
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
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FDA UNII
M7GSN5Q1M6
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
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MESH
C004363
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
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SMS_ID
100000159545
Created by admin on Fri Dec 15 18:35:59 GMT 2023 , Edited by admin on Fri Dec 15 18:35:59 GMT 2023
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