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4-Iodo Suberoylanilide HydroxaMic Acid

Product Name
4-Iodo Suberoylanilide HydroxaMic Acid
CAS No.
1219807-87-0
Chemical Name
4-Iodo Suberoylanilide HydroxaMic Acid
Synonyms
4-iodo-SAHA;4-Iodo Suberoylanilide HydroxaMic Acid;N1-Hydroxy-N8-(4-iodophenyl)octanediaMide;Octanediamide, N1-hydroxy-N8-(4-iodophenyl)-
CBNumber
CB32544804
Molecular Formula
C14H19IN2O3
Formula Weight
390.22
MOL File
1219807-87-0.mol
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4-Iodo Suberoylanilide HydroxaMic Acid Property

Density 
1.579±0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
insoluble in H2O; insoluble in EtOH; ≥1.67 mg/mL in DMSO
form 
A crystalline solid
pka
9.48±0.20(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
10495
Product name
4-iodo-SAHA
Purity
≥98%
Packaging
50mg
Price
$89
Updated
2024/03/01
Cayman Chemical
Product number
10495
Product name
4-iodo-SAHA
Purity
≥98%
Packaging
100mg
Price
$168
Updated
2024/03/01
Cayman Chemical
Product number
10495
Product name
4-iodo-SAHA
Purity
≥98%
Packaging
250mg
Price
$395
Updated
2024/03/01
Cayman Chemical
Product number
10495
Product name
4-iodo-SAHA
Purity
≥98%
Packaging
500mg
Price
$700
Updated
2024/03/01
Usbiological
Product number
014903
Product name
4-Iodo Suberoylanilide Hydroxamic Acid
Packaging
100mg
Price
$446
Updated
2021/12/16
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4-Iodo Suberoylanilide HydroxaMic Acid Chemical Properties,Usage,Production

Uses

A SAHA derivative with antiproliferative activity in several human cancer cell lines. Antitumor agent.

Biological Activity

4-iodo-saha is a hydrophobic derivative of saha, the class i and class ii histone deacetylase (hdac) inhibitor [1].the reversible acetylation of lysine residues in histone plays an important role in transcriptional activation and repression. the regulation of these post-translational modifications is balanced by histone acetyltransferase (hat) and histone deacetylase (hdac) activities. hdacs are also involved in reversible acetylation of non-histone proteins [1].4-iodo-saha is a histone deacetylase (hdac) inhibitor. in skbr3-breast-derived cell line, 4-iodo-saha inhibited cell proliferation with ec50 value of 1.1 μm. in ht29 colon-derived cell line, leukemia-derived u937 tumor cell line, ja16, hl60 and k562 cell lines, 4-iodo-saha inhibited cell proliferation with ec50 values of 0.95, 0.12, 0.24, 0.85 and 1.3 μm, respectively. 4-iodo-saha is 10-fold more potent as an inhibitor of u937 leukemia cell proliferation compared to saha (0.12 μm versus 1.2 μm). in skbr3 cells, 4-iodo-saha reduced acetylated h4 and p21 levels [1].

References

[1]. salmi-smail c, fabre a, dequiedt f, et al. modified cap group suberoylanilide hydroxamic acid histone deacetylase inhibitor derivatives reveal improved selective antileukemic activity. j med chem. 2010 apr 22;53(8):3038-47.

4-Iodo Suberoylanilide HydroxaMic Acid Preparation Products And Raw materials

Raw materials

Preparation Products

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4-Iodo Suberoylanilide HydroxaMic Acid Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
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86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
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94838
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Chemsky (shanghai) International Co.,Ltd
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
15421
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60
Shanghai TaoSu Biochemical Technology Co., Ltd.
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021-33632979
Fax
021-34692979
Email
info@tsbiochem.com
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China
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8073
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Shenzhen Polymeri Biochemical Technology Co., Ltd.
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+86-400-002-6226 13028896684
Email
sales@rrkchem.com
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China
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55896
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ChemeGen(Shanghai) Biotechnology Co.,Ltd.
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18818260767
Fax
QQ 3610331285
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sales@chemegen.com
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Energy Chemical
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021-58432009 400-005-6266
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021-58436166
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marketing1@energy-chemical.com
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China
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44894
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MedBioPharmaceutical Technology Inc
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021-69568360 18916172912
Email
order@med-bio.cn
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China
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InvivoChem
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13549236410
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sales@invivochem.cn
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China
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TargetMol Chemicals Inc.
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4008200310
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marketing@tsbiochem.com
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China
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24024
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Shaoguan Qicheng Biotechnology Co., Ltd
Tel
18122215013
Email
780229652@qq.com
Country
China
ProdList
939
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58

1219807-87-0, 4-Iodo Suberoylanilide HydroxaMic AcidRelated Search:


  • 4-Iodo Suberoylanilide HydroxaMic Acid
  • 4-iodo-SAHA
  • N1-Hydroxy-N8-(4-iodophenyl)octanediaMide
  • Octanediamide, N1-hydroxy-N8-(4-iodophenyl)-
  • 1219807-87-0
  • C14H19IN2O3
  • Amines, Aromatics, Inhibitors, Pharmaceuticals, Intermediates & Fine Chemicals
  • Amines
  • Aromatics
  • Inhibitors
  • Intermediates & Fine Chemicals
  • Pharmaceuticals