Suberohydroxamic acid
Synonym(s):N,N′-Dihydroxyoctanediamide;SBHA;SBHA - CAS 38937-66-5 - Calbiochem;Suberic Bishydroxamate, Suberoyl Bishydroxamic Acid, HDAC Inhibitor XII;Suberoyl bis-hydroxamic acid
- CAS NO.:38937-66-5
- Empirical Formula: C8H16N2O4
- Molecular Weight: 204.22
- MDL number: MFCD00192455
- SAFETY DATA SHEET (SDS)
- Update Date: 2024-11-18 17:01:59
What is Suberohydroxamic acid?
Description
Suberohydroxamic acid (SBHA) is a competitive histone deacetylase (HDAC) inhibitor that has been shown to inhibit HDAC1 (IC50 = 0.25 μM) and HDAC3 (IC50 = 0.30 μM). SBHA causes cell differentiation, cell cycle arrest, or apoptosis. HDAC inhibitors, including SBHA, act synergistically to kill cancer cells when used in combination with cytostatic drugs, allowing lower doses of both inhibitors and drugs to be used.
The Uses of Suberohydroxamic acid
Histone deacetylase inhibitor. A cell-permeable inhibitor of HDAC1 and HDAC3. Shown to suppresses the growth of proliferating keratinocytes and squamous cell carcinoma cells.
The Uses of Suberohydroxamic acid
Inhibits histone deacetylation.
What are the applications of Application
Suberoyl bis-hydroxamic Acid is Inhibits histone deacetylation
Definition
ChEBI: N,N'-dihydroxyoctanediamide is a hydroxamic acid.
Biological Activity
Suberoyl bis-hydroxamic acid (SBHA) is a Histone deacetylase (HDAC) inhibitor. SBHA inhibits the activity of HDAC1 and HDAC3 with IC50 values of 250 and 300 nM, respectively. SBHA inhibits proliferation, and induces apoptosis in several cancer cell lines. SBHA has been shown to activate Notch signaling in medullary thyroid carcinoma (MTC) cells.
Biochem/physiol Actions
Suberoyl bis-hydroxamic acid (SBHA) is a Histone deacetylase (HDAC) inhibitor. SBHA inhibits the activity of HDAC1 and HDAC3 with IC50 values of 250 and 300 nM, respectively. SBHA inhibits proliferation, and induces apoptosis in several cancer cell lines. SBHA has been shown to activate Notch signaling in medullary thyroid carcinoma (MTC) cells.
References
1. richon vm, emiliani s, verdin e et al. a class of hybrid polar inducers of transformed cell differentiation inhibits histone deacetylases. proc natl acad sci u s a. 1998 mar 17; 95(6):3003-7.2. zhang xd, gillespie sk, borrow jm, hersey p. the histone deacetylase inhibitor suberic bishydroxamate regulates the expression of multiple apoptotic mediators and induces mitochondria-dependent apoptosis of melanoma cells. mol cancer ther. 2004 apr; 3(4):425-35.
Properties of Suberohydroxamic acid
Melting point: | 153-155 °C(lit.) |
Density | 1.219±0.06 g/cm3(Predicted) |
storage temp. | −20°C |
solubility | H2O: soluble |
pka | 9.18±0.20(Predicted) |
form | lyophilized powder |
color | White to Light Beige |
Stability: | Hygroscopic |
Safety information for Suberohydroxamic acid
Computed Descriptors for Suberohydroxamic acid
New Products
4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Diclofenac Potassium Ornidazole IP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Aceclofenac IP/BP/EP Nimesulide BP SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION AMOXICILLIN (AMOXYCILLIN) TRIHYDRATE Methylcobalamin (vitamin B12) SODIUM VALPROATE SODIUM METHYL PARABEN LAMOTRIGINERelated products of tetrahydrofuran
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