ChemicalBook > CAS DataBase List > WEDELOLACTONE

WEDELOLACTONE

Product Name
WEDELOLACTONE
CAS No.
524-12-9
Chemical Name
WEDELOLACTONE
Synonyms
Wedelolactone;Wedelia lactone;Wedelolactone CRS;Wedelolactone, ≥98%(HPLC);IKK Inhibitor II, Wedelolactone;5,11,12-Trihydroxy-7-MethoxycouMestan;Wedelolactone, 98%, from Wedelia chinensis (Osbeck.) Merr.;1,8,9-trihydroxy-3-Methoxy-6H-benzofuro[3,2-c]chroMen-6-one;IKK Inhibitor II, Wedelolactone - CAS 524-12-9 - Calbiochem;1,8,9-trihydroxy-3-methoxy-[1]benzofuro[3,2-c]chromen-6-one
CBNumber
CB1505300
Molecular Formula
C16H10O7
Formula Weight
314.25
MOL File
524-12-9.mol
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WEDELOLACTONE Property

Melting point:
327~330℃
Boiling point:
498.4±45.0 °C(Predicted)
Density 
1.655±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO: 14 mg/mL, soluble
form 
solid
pka
6.90±0.20(Predicted)
color 
brown-beige
InChIKey
XQDCKJKKMFWXGB-UHFFFAOYSA-N
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Safety

Hazard Codes 
Xn
Risk Statements 
22-43
Safety Statements 
36/37
WGK Germany 
3
HS Code 
29322090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W4016
Product name
Wedelolactone
Purity
≥98% (HPLC), powder
Packaging
1mg
Price
$166
Updated
2024/03/01
TCI Chemical
Product number
W0015
Product name
Wedelolactone
Packaging
1MG
Price
$117
Updated
2024/03/01
TCI Chemical
Product number
W0015
Product name
Wedelolactone
Packaging
10MG
Price
$525
Updated
2024/03/01
Cayman Chemical
Product number
11796
Product name
Wedelolactone
Purity
≥98%
Packaging
500μg
Price
$49
Updated
2024/03/01
Cayman Chemical
Product number
11796
Product name
Wedelolactone
Purity
≥98%
Packaging
1mg
Price
$82
Updated
2024/03/01
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WEDELOLACTONE Chemical Properties,Usage,Production

Uses

Wedelolactone is inhibits caspase-11; a key regulator of proinflammatory cytokine IL-1β maturation and apoptosis.

Definition

ChEBI: A member of the class of coumestans that is coumestan with hydroxy substituents as positions 1, 8 and 9 and a methoxy substituent at position 3.

Biological Activity

wedelolactone is an inhibitor of ikk.ikb kinase (ikk) complex contains the catalytic subunits ikkα and ikkβ, and the regulatory subunit ikkγ/nemo. ikk, is a kinase critical for activation of nf-κb by mediating phosphorylation and degradation of iκbα. the induction of caspase-11 is an important upstream controlling event in inflammatory response and apoptosis under pathological conditions modulated by upstream nf-κb-mediated transcription[1].

Biochem/physiol Actions

Wedelolactone inhibits NF-κB-mediated gene transcription in cells by blocking the phosphorylation and degradation of IκBα. Irreversible inhibitor of IKKα and β kinase activity (IC50 < 10 μM). Wedelolactone has no effects on p38 MAP kinase or Akt.

in vitro

in cultured mouse balb/c 3t3 cells, mouse splenocytes and hela cells, wedelolactone (0~100 μm) inhibited lps-induced caspase-11 expression by inhibiting nf-κb-mediated transcription through the direct inhibition of ikk. wedelolactone played an potential role in anti-inflammatory therapy to inhibit il-1β levels in diseases such as rheumatoid arthritis, asthma and septic shock[1].

in vivo

on swiss albino male mouse skin, ikk inhibition by wedelolactone (10 μm) prevented the induction of nf-κb, perturbed the generation of reactive oxygen species and reactive nitrogen intermediates, blunted the signal transduction that lead to the activation of the early immediate genes, and thereby protected mouse skin from the uvb induced neoplastic transformation, angiotropism and metastatic progression [2].

References

[1] kobori m, yang z, gong d, et al. wedelolactone suppresses lps-induced caspase-11 expression by directly inhibiting the ikk complex.[j]. cell death & differentiation, 2004, 11(1):123-30.
[2] ali f, khan b a, sultana s. wedelolactone mitigates uvb induced oxidative stress, inflammation and early tumor promotion events in murine skin: plausible role of nfκb pathway[j]. european journal of pharmacology, 2016, 786:253-264.

WEDELOLACTONE Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from WEDELOLACTONE manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
Wedelolactone 524-12-9
Price
US $0.00-0.00/KG
Min. Order
5mg
Purity
99%HPLC
Supply Ability
2000tons
Release date
2020-01-06
Shaanxi Dideu Medichem Co. Ltd
Product
SkiMMin 524-12-9
Price
US $0.00-0.00/KG
Min. Order
5mg
Purity
99%HPLC
Supply Ability
2000tons
Release date
2020-01-06
Shanghai Standard Technology Co., Ltd.
Product
Wedelolactone 524-12-9
Price
US $0.00/mg
Min. Order
5mg
Purity
≥98%(HPLC)
Supply Ability
10 g
Release date
2019-11-22

524-12-9, WEDELOLACTONERelated Search:


  • Wedelolactone, ≥98%(HPLC)
  • IKK Inhibitor II, Wedelolactone - CAS 524-12-9 - Calbiochem
  • 1,8,9-Trihydroxy-3-methoxy-6H-benzofuro[3,2-c][1]benzopyran-6-one
  • Wedelolactone
  • 6H-Benzofuro(3,2-C)(1)benzopyran-6-one, 1,8,9-trihydroxy-3-methoxy-
  • 5,11,12-Trihydroxy-7-MethoxycouMestan
  • 1,8,9-trihydroxy-3-Methoxy-6H-benzofuro[3,2-c]chroMen-6-one
  • IKK Inhibitor II, Wedelolactone
  • Wedelia lactone
  • Wedelolactone, 98%, from Wedelia chinensis (Osbeck.) Merr.
  • Wedelolactone CRS
  • 1,8,9-trihydroxy-3-methoxy-[1]benzofuro[3,2-c]chromen-6-one
  • 1,8,9-Trihydroxy-3-methoxy-6H-benzofuro[3,2-c]chromen-6-one[Wedelolactone
  • 524-12-9
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract