ChemicalBook > CAS DataBase List > (E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA)

(E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA)

Product Name
(E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA)
CAS No.
131359-24-5
Chemical Name
(E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA)
Synonyms
HBB2;2-HBA;abs820538;2-HBA Exclusive;bis(2-hydroxybenzylidene)acetone;(E,E)-Bis(2-hydroxybenzylidene)acetone;inhibit,2-HBA,Inhibitor,Caspase,2HBA,2 HBA;(E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA);(E,E)-Bis(2-hydroxybenzylidene)acetone\n(2-HBA);(1E,4E)-1,5-Bis(2-hydroxyphenyl)penta-1,4-dien-3-one
CBNumber
CB32653829
Molecular Formula
C17H14O3
Formula Weight
266.29
MOL File
131359-24-5.mol
More
Less

(E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA) Property

storage temp. 
Sealed in dry,Store in freezer, under -20°C
solubility 
DMSO: soluble15mg/mL (clear solution)
form 
powder
color 
white to beige
InChIKey
YNVAHBUBGBLIEY-WGDLNXRISA-N
More
Less

Safety

WGK Germany 
3
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML0456
Product name
HBB2
Purity
≥98% (HPLC)
Packaging
5mg
Price
$86.9
Updated
2022/05/15
Sigma-Aldrich
Product number
SML0456
Product name
HBB2
Purity
≥98% (HPLC)
Packaging
25mg
Price
$337
Updated
2022/05/15
Cayman Chemical
Product number
11879
Product name
2-HBA
Purity
≥98%
Packaging
5mg
Price
$65
Updated
2024/03/01
Cayman Chemical
Product number
11879
Product name
2-HBA
Purity
≥98%
Packaging
10mg
Price
$121
Updated
2024/03/01
Cayman Chemical
Product number
11879
Product name
2-HBA
Purity
≥98%
Packaging
50mg
Price
$505
Updated
2024/03/01
More
Less

(E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA) Chemical Properties,Usage,Production

Description

Nrf2 activation of the antioxidant response element (ARE) is central to cytoprotective gene expression against oxidative and/or electrophilic stress. Unless activated by inflammatory, environmental, or oxidative stressors, Nrf2 is sequestered in the cytoplasm by its repressor, Keap1. Because of its protective capabilities, small molecules that activate Nrf2 signaling are being examined as potential anti-cancer or anti-inflammatory agents. 2-HBA, a synthetic analog of curcumin, is an indirect inducer of enzymes that catalyze detoxification reactions through the Keap1-Nrf2-ARE pathway. As a double Michael reaction acceptor, 2-HBA can directly modify cysteine sulfhydryl groups in Keap1 and consequently suppress Nrf2 ubiquitination, which leads to enhanced expression of antioxidative and cytoprotective enzymes. 2-HBA doubles the specific activity of NAD(P)H:quinone acceptor oxidoreductase 1 (NQO1) in Hepa1c1c7 cells at 0.15 μM. In rapidly dividing mouse leukemia L1210 cells, 0.6 μM 2-HBA increases the activities of NQO1, glutathione reductase, and the levels of total glutathione. At 5-15 μM, 2-HBA causes G2/M cell cycle arrest and p53-independent, caspase 3-mediated apoptosis.

Uses

(E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA) is a synthetic analogue of curcumin that displays strong NAD(P)H:quinone reductase (NQO1) inducer potency in Hepa 1c1c7 cells. 2-HBA, a double Michael reaction acceptor, can directly modify cysteine sulfhydryl groups in Keap1 and consequently suppress Nrf2 ubiquitination which in turn enhances the expression of antioxidative and cytoprotective enzymes. 2-HBA has also been shown to cause G2/M cell cycle arrest and p53-independent, caspase 3-mediated apoptosis.

in vitro

2-hba could markedly increase the activities of nad(p)h:quinone acceptor oxidoreductase 1 (nqo1) and glutathione reductase, the levels of total glutathione, as well as the phase 2 response markers. in addition, at high concentrations 2-hba caused g2/m cell cycle arrest and apoptosis. moreover, the mutant l1210 cell line was found to be more sensitive to the apoptotic effects of 2-hba [1].

in vivo

the effect of 2-hba on the dmba-induced expression of the ha-ras gene in isolated rna tissues of cba/ca inbred mice was investigated. according to the previous findings, elevated ha-ras expression was obserrved even 24 h after dmba treatment. administration of 2-hba with dmba could lead to a decrease of the dmba-induced ha-ras gene expression in all the investigated tissues, suggesting metabolic interaction of 2-hba and dmba. in addiiton, administration of 2-hba 24 h prior to the dmba treatment was able to reduce the ha-ras gene expression in all tested tissues except the liver, which could be the result of a possible cyp1a inducer and pro-oxidant effects of 2-hba [2].

References

[1] a. t. dinkova-kostova, a. h. cory, r. e. bozak, et al. bis(2-hydroxybenzylidene)acetone, a potent inducer of the phase 2 response, causes apoptosis in mouse leukemia cells through a p53-independent, caspase-mediated pathway. cancer letters 245, 341-349 (2007).
[2] perjési p, ember i, bozak re, nádasi e, rozmer z, varjas t, hicks rj. effect of the chalcone analog e,e-bis(2-hydroxybenzylidene) acetone on the 7,12-dimethylbenz[a]anthracene-induced ha-ras gene activity in vivo. in vivo. 2006 jan-feb;20(1):141-6.

(E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA) Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

(E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA) Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94838
Advantage
76
MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4863
Advantage
58
Shanghai TaoSu Biochemical Technology Co., Ltd.
Tel
021-33632979
Fax
021-34692979
Email
info@tsbiochem.com
Country
China
ProdList
8073
Advantage
58
ShangHai Biochempartner Co.,Ltd
Tel
17754423994 17754423994
Fax
QQ:2853530913
Email
2853530910@QQ.com
Country
China
ProdList
8012
Advantage
62
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Fax
010-60605840
Email
psaitong@jm-bio.com
Country
China
ProdList
12308
Advantage
58
MQ (shanghai) Pharmaceuticals Co., Ltd.
Tel
13761635123
Fax
1014988033@qq
Email
1014988033@qq.com
Country
China
ProdList
4979
Advantage
55
Angel Pharmatech, Ltd.
Tel
17317130613
Fax
QQ3358272972
Email
3358272972@qq.com
Country
China
ProdList
3238
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 13028896684
Email
sales@rrkchem.com
Country
China
ProdList
55896
Advantage
58
Fan De(Beijing) Biotechnology Co., Ltd.
Tel
15911056312
Email
liming@bio-fount.com
Country
China
ProdList
9730
Advantage
58
Jiangsu aikang biomedical research and development co., LTD
Tel
025-66110311 13155353615
Email
qzhang@aikonchem.com
Country
China
ProdList
15527
Advantage
58

131359-24-5, (E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA)Related Search:


  • (E,E)-Bis(2-hydroxybenzylidene)acetone (2-HBA)
  • (1E,4E)-1,5-Bis(2-Hydroxyphenyl)-1,4-pentadien-3-one
  • HBB2
  • 2-HBA
  • (E,E)-Bis(2-hydroxybenzylidene)acetone\n(2-HBA)
  • 2-HBA Exclusive
  • bis(2-hydroxybenzylidene)acetone
  • 1,4-Pentadien-3-one, 1,5-bis(2-hydroxyphenyl)-, (1E,4E)-
  • (E,E)-Bis(2-hydroxybenzylidene)acetone
  • abs820538
  • (1E,4E)-1,5-Bis(2-hydroxyphenyl)penta-1,4-dien-3-one
  • inhibit,2-HBA,Inhibitor,Caspase,2HBA,2 HBA
  • 131359-24-5
  • Aromatics
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Aromatics, Pharmaceuticals, Intermediates & Fine Chemicals