112522-64-2 4-Acetylamino-N-(2'-aminophenyl)benzamide CAS NO.112522-64-2
- FOB Price: USD: 1,000.00-1,000.00 /Metric Ton Get Latest Price
- Min.Order: 1 Kilogram
- Payment Terms: L/C,T/T
- Available Specifications:
pharma(0-1)Metric Ton
- Product Details
Keywords
- 112522-64-2
- 4-Acetylamino-N-(2'-aminophenyl)benzamide
- C15H15N3O2
Quick Details
- ProName: 112522-64-2 4-Acetylamino-N-(2'-aminop...
- CasNo: 112522-64-2
- Molecular Formula: C15H15N3O2
- Appearance: white powder
- Application: pharma
- DeliveryTime: prompt
- PackAge: as clients needs
- Port: Shanghai,QingdaoTianjin,Guangzhou
- ProductionCapacity: 1 Metric Ton/Day
- Purity: 99%
- Storage: RT
- Transportation: sea
- LimitNum: 1 Kilogram
- Moisture Content: N/A
- Impurity: N/A
- N/A: N/A
Superiority
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4.Customs Synthesis
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Details
4-Acetylamino-N-(2'-aminophenyl)benzamide Chemical Properties
RTECS CU8702023
storage temp. Store at +4°C
solubility Soluble in DMSO
color off-white
Sensitive Air Sensitive
Safety Information
Hazard Codes Xi
Risk Statements 36
Safety Statements 26
MSDS Information
4-Acetylamino-N-(2'-aminophenyl)benzamide Usage And Synthesis
Uses Tacedinaline is a histone deacetylase (HDAC) inhibitor. Tacedinaline is an anti-cancer agent as HDAC inhibitors block angiogenesis, arrest cell growth, and lead to differentiation and apoptosis in tum or cells. Studies show Tacedinaline to be effective against acute myeloid leukemia in vitro and in vivo when used in combination with conventional anti-cancer agents.
Definition ChEBI: A benzamide obtained by formal condensation of the carboxy group of 4-acetamidobenzoic acid with one of the amino groups of 1,2-phenylenediamine. An oral cytostatic drug with impressive differential activity against leukemic cells and normal stem-cells. Al o used in combination therapy for selected tumors including non-smoll cell lung, pancreatic, breast, and colorectal cancers.
Biological Activity Orally active histone deacetylase (HDAC) inhibitor (K i values are 0.41, 0.75, >100 and >100 μ M for HDAC1, HDAC3, HDAC6 and HDAC8 respectively). Mediates G 1 cell cycle arrest, inhibits proliferation and induces apoptosis in vitro and in vivo .