CAS 2430-27-5; 丙戊酰胺; 2-propyl-valeramid

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货号

品牌

产品名称

规格

包装、参考价格

V873729

MACKLIN

2-丙基戊酰胺

97%

40元/50mg; 116元/250mg; 328元/1g; 1335元/5g;

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储存：-20℃
状态：白色到灰白色粉末

V793630

MACKLIN

2-丙基戊酰胺

10mM in DMSO

456元/1ml;

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储存：-20°C

L08847

Alfa Aesar

2,2-Di-n-propylacetamide

97%

795元/5g; 5766元/25g;

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应用
It is employed as an antiepileptic drug. It is hydrolyzed quickly to VPA in vivo, but has intrinsic anticonvulsant activity. Also a reactant used in the synthesis of mutual prodrugs containing bio-cleavable and drug releasable disulfide linkers.

备注
Store in cool. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.

基本信息

MDL
MFCD00051534

EINECS
219-394-2

分子式
C₈H₁₇NO

分子量
143.23

熔点
123-127°

灵敏度
Ambient temperatures.

溶解性
Soluble in chloroform, dimethyl sulfoxide and methanol. Insoluble in water.

Beilstein
1750444

Merck
14,9914

GHS危害和防范说明

GHS符号

Hazard Statements
H302
Harmful if swallowed.

Precautionary Statements
P264-P270-P301+P312a-P330-P501a
Wash thoroughly after handling.Do not eat, drink or smoke when using this product.Do not eat, drink or smoke when using this product.Rinse mouth.Dispose of contents/container in accordance with local/regional/national/international regulations.

安全信息

危险类别
22
Harmful if swallowed.

安全等级
36
Wear suitable protective clothing.

欧盟危险品标志

RTECS
YV5965500

TSCA
否

V3640

Sigma-Aldrich

Valpromide

≥97% (NMR)

1012.81元/10 MG; 4075.16元/50 MG;

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产品说明

应用

Valpromide has been used to pretreat NIH/3T3 cells to test its effect on cytomegalovirus (CMV) viral replication. It has also been used to test its antiviral functionality in herpes simplex virus type 1 (HSV-1) infected human oligodendroglioma (HOG) cells. It may be used to test its effect on apoptosis induction in astrocytes.

包装

10, 50 mg in glass bottle

生化/生理作用

Valpromide (VPD) is a derivative of valproic acid (VPA) and is used as an antiepileptic drug. It is hydrolyzed quickly to VPA in vivo, but has intrinsic anticonvulsant activity.
Valpromide possesses antipsychotic property. It lacks the toxic and teratogenic effects of valproic acid. It also lacks the histone deacetylase (HDAC) inhibitory activity of valproic acid.

特点和优势

This compound was developed by Sanofi Aventis. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

基本信息

经验(实验)分子式	C₈H₁₇NO
分子量	143.23
MDL编号	MFCD00051534
PubChem化学物质编号	329829044
NACRES	NA.77

产品性质

质量水平	100
测定	≥97% (NMR)
形式	powder
颜色	white to off-white
溶解性	DMSO: >10 mg/mL
创始人	Sanofi Aventis
储存温度	room temp
SMILES string	CCCC(CCC)C(N)=O
InChI	1S/C8H17NO/c1-3-5-7(6-4-2)8(9)10/h7H,3-6H2,1-2H3,(H2,9,10)
InChI key	OMOMUFTZPTXCHP-UHFFFAOYSA-N

安全信息

象形图
警示用语：	Warning
危险声明	H302
预防措施声明	P264 - P270 - P301 + P312 + P330 - P501
危险分类	Acute Tox. 4 Oral
储存分类代码	11 - Combustible Solids
WGK	WGK 3
闪点(F)	Not applicable
闪点(C)	Not applicable

544374

Fluorochem

2-Propylpentanamide

97+%

242元/250mg; 572元/1g;

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基本信息

CAS Number	2430-27-5
MDL Number	MFCD00051534