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Coumarin suberoylanilide hydroxamic acid
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Coumarin suberoylanilide hydroxamic acid

CAS: 1260635-77-5

Ref. 3D-FC20573

5mgDiscontinued
10mgDiscontinued
25mgDiscontinued
50mgDiscontinued
100mgDiscontinued

Discontinued product. For inquiries about similar products, please fill out our form or email us at .


Product Information

Name:
Coumarin suberoylanilide hydroxamic acid
Synonyms:
  • N1-Hydroxy-N8-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)octanediamideCoumarin-SAHA
Description:

Coumarin suberoylanilide hydroxamic acid (CSHA) is a hydroxamic compound that is used in cancer research. It inhibits the activity of histone deacetylases, which are enzymes that remove acetyl groups from lysine residues on histones and other proteins. CSHA has been shown to inhibit the growth of tumor cells by decreasing the expression of genes involved in energy transfer, DNA synthesis, and RNA synthesis. The fluorescent probe CSHA can be used to study the localization of these enzymes in cells. Coumarin-saha is a derivative of CSHA that has been modified to have an affinity for cysteine residues found in proteins such as histones and RACK1. Coumarin-saha has also been shown to inhibit the activity of some enzymes involved in DNA replication such as DNA polymerase alpha and beta.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
346.38 g/mol
Formula:
C18H22N2O5
Purity:
Min. 95%
Color/Form:
Powder
InChI:
InChI=1S/C18H22N2O5/c1-12-10-18(23)25-15-11-13(8-9-14(12)15)19-16(21)6-4-2-3-5-7-17(22)20-24/h8-11,24H,2-7H2,1H3,(H,19,21)(H,20,22)
InChI key:
InChIKey=YSRCADVJNRJJAV-UHFFFAOYSA-N
SMILES:
Cc1cc(=O)oc2cc(NC(=O)CCCCCCC(=O)NO)ccc12
MDL:
Melting point:
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Density:
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EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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