- Scriptaid
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- $65.00 / 5mg
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2026-01-13
- CAS:287383-59-9
- Min. Order:
- Purity: 98.05%
- Supply Ability: 10g
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| | SCRIPTAID Basic information |
| | SCRIPTAID Chemical Properties |
| Melting point | 160-161 °C | | density | 1.338±0.06 g/cm3(Predicted) | | storage temp. | -20°C | | solubility | Soluble in DMSO (up to 4 mg/ml). | | form | Yellow solid. | | pka | 9.46±0.20(Predicted) | | color | White | | biological source | synthetic (organic) | | Sensitive | Light Sensitive | | Stability: | Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 2 months. | | InChI | InChI=1S/C18H18N2O4/c21-15(19-24)10-2-1-3-11-20-17(22)13-8-4-6-12-7-5-9-14(16(12)13)18(20)23/h4-9,24H,1-3,10-11H2,(H,19,21) | | InChIKey | JTDYUFSDZATMKU-UHFFFAOYSA-N | | SMILES | C1(=O)C2=C3C(C=CC=C3C(=O)N1CCCCCC(NO)=O)=CC=C2 |
| WGK Germany | 3 | | Storage Class | 11 - Combustible Solids |
| | SCRIPTAID Usage And Synthesis |
| Description | Scriptaid is a histone deacetylase inhibitor that has an optimal concentration of 6-8 μM in a cell-based assay, is less toxic than trichostatin A, and works in a wide variety of biological systems. It induces cell cycle arrest in colon cancer cells in culture and inhibits tumor growth in vitro and in vivo. Scriptaid also facilitates the cloning of inbred mouse strains produced by somatic cell nuclear transfer. | | Uses | Scriptaid has been used in post activation of oocytes and embryo culture. | | Uses | Histone deacetylase inhibitor. A cell-permeable, relatively non-toxic HDAC inhibitor that facilitates transcriptional activation (TGFβ/Smad4) in both stable and transient receptor assays in a concentration-dependent manner. | | Definition | ChEBI: 6-(1,3-dioxo-2-benzo[de]isoquinolinyl)-N-hydroxyhexanamide is a member of isoquinolines. | | General Description | Scriptaid is a histone deacetylase (HDAC) inhibitor, which enhances global acetylation of histones. It improves transcriptional activity and protein expression. Scriptaid inhibits tumor growth. It decreases telomerase activity and stimulates glioma cell apoptosis. | | Biological Activity | Novel histone deacetylase inhibitor. Produces > 100-fold increase in histone acetylation and displays relatively low toxicity. | | Biochem/physiol Actions | Histone deacetylase inhibitor with lower toxicity than trichostatin A; used to enhance protein expression. | | References | [1] G H SU. A novel histone deacetylase inhibitor identified by high-throughput transcriptional screening of a compound library.[J]. Cancer research, 2000, 60 12: 3137-3142.
[2] KELLY HUBER. Inhibitors of histone deacetylases: correlation between isoform specificity and reactivation of HIV type 1 (HIV-1) from latently infected cells.[J]. The Journal of Biological Chemistry, 2011: 22211-22218. DOI:10.1074/jbc.m110.180224
[3] EUN JU LEE. Histone deacetylase inhibitor scriptaid induces cell cycle arrest and epigenetic change in colon cancer cells.[J]. International journal of oncology, 2008, 15 1: 767-776. DOI:10.3892/ijo\_00000063
[4] VITOR BRAGA RISSI. Inhibition of RNA synthesis during Scriptaid exposure enhances gene reprogramming in SCNT embryos.[J]. Reproduction, 2019, 157 2: 123-133. DOI:10.1530/rep-18-0366
[5] SONG HUANG. Scriptaid/exercise-induced lysine acetylation is another type of posttranslational modification occurring in titin.[J]. Journal of applied physiology, 2020: 276-285. DOI:10.1152/japplphysiol.00617.2019 |
| | SCRIPTAID Preparation Products And Raw materials |
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