N-Phenethylbenzamide

Name: N-Phenethylbenzamide
Brand: MedChemExpress
SKU: HY-32135
Rating: 4.5 (0 reviews)

Cat. No.: HY-32135 Purity: 99.56%: Data Sheet
COA

SDS
Handling Instructions
FAQs
Technical Support

N-Phenethylbenzamide is an active compound. N-Phenethylbenzamide can be extracted from Liriodendron tulipifera. N-Phenethylbenzamide can be used for the research of inflammatory diseases.

연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.

N-Phenethylbenzamide 화학구조

CAS No. : 3278-14-6

사이즈	재고	수량
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO ready for reconstitution	해외재고보유	Estimated Time of Arrival: December 31
Solution
10 mM * 1 mL in DMSO	해외재고보유	Estimated Time of Arrival: December 31
Solid
5 g	해외재고보유	Estimated Time of Arrival: December 31
10 g	해외재고보유	Estimated Time of Arrival: December 31
25 g	해외재고보유	Estimated Time of Arrival: December 31
50 g	견적 받기

or 대량구매 문의

* 장바구니에 담기 전 물품의 수량을 선택해 주십시오.

This product is a controlled substance and not for sale in your territory.

고객리뷰

Based on 1 Customer Validation

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•Related Small Molecules:

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Biological Activity
순도&문서
References
고객리뷰

제품 설명

N-Phenethylbenzamide is an active compound. N-Phenethylbenzamide can be extracted from Liriodendron tulipifera. N-Phenethylbenzamide can be used for the research of inflammatory diseases^[1].

Cellular Effect

Cell Line	Type	Value	Description	References
RAW264.7	IC₅₀	>50 3 Compound: 30	Antiinflammatory activity in mouse RAW264.7 assessed as inhibition of LPS-induced NO production preincubated for 30 mins followed by LPS stimulation measured after 24 hrs by Griess reagent based assay Antiinflammatory activity in mouse RAW264.7 assessed as inhibition of LPS-induced NO production preincubated for 30 mins followed by LPS stimulation measured after 24 hrs by Griess reagent based assay	[PMID: 33939429]
RAW264.7	IC₅₀	> 50 3 Compound: 30	Antiinflammatory activity in mouse RAW264.7 assessed as inhibition of LPS-induced NO production preincubated for 30 mins followed by LPS stimulation measured after 24 hrs by Griess reagent based assay Antiinflammatory activity in mouse RAW264.7 assessed as inhibition of LPS-induced NO production preincubated for 30 mins followed by LPS stimulation measured after 24 hrs by Griess reagent based assay	[PMID: 33939429]
RAW264.7	IC₅₀	> 50 3 Compound: 30	Antiinflammatory activity in mouse RAW264.7 assessed as inhibition of LPS-induced NO production preincubated for 30 mins followed by LPS stimulation measured after 24 hrs by Griess reagent based assay Antiinflammatory activity in mouse RAW264.7 assessed as inhibition of LPS-induced NO production preincubated for 30 mins followed by LPS stimulation measured after 24 hrs by Griess reagent based assay	[PMID: 33939429]

In Vitro

N-Phenethylbenzamide inhibits LPS-induced NO production with IC₅₀ value of ＞50 μM^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

분자량

225.29

화학식

C₁₅H₁₅NO

CAS No.

3278-14-6

Appearance

Solid

Color

White to off-white

SMILES

O=C(NCCC1=CC=CC=C1)C2=CC=CC=C2

Structure Classification

Others

Initial Source

선적

Room temperature in continental US; may vary elsewhere.

보관

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	2 years
	-20°C	1 year

용액&용해도

In Vitro:

DMSO : 50 mg/mL (221.94 mM; ultrasonic and warming and heat to 80°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions

Concentration Solvent Mass	1 mg	5 mg	10 mg

1 mM	4.4387 mL	22.1936 mL	44.3872 mL
5 mM	0.8877 mL	4.4387 mL	8.8774 mL
10 mM	0.4439 mL	2.2194 mL	4.4387 mL

View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

몰농도 계산기
농도 희석 계산기

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

Concentration _(start)

Volume _(start)

Concentration _(final)

Volume _(final)

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Calculation results:

Working solution concentration: mg/mL

순도&문서

Purity: 99.56%

Select Batch:

Data Sheet (268 KB) SDS (393 KB)

COA (245 KB) LCMS (265 KB)

Handling Instructions (2659 KB)

References

[1]. InWha Park, et al. Tulipiferamide A, an Alkamide from Liriodendron tulipifera, Exhibits an Anti-Inflammatory Effect via Targeting IKKβ Phosphorylation. J Nat Prod [Content Brief]

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg

DMSO	1 mM	4.4387 mL	22.1936 mL	44.3872 mL	110.9681 mL
	5 mM	0.8877 mL	4.4387 mL	8.8774 mL	22.1936 mL
	10 mM	0.4439 mL	2.2194 mL	4.4387 mL	11.0968 mL
	15 mM	0.2959 mL	1.4796 mL	2.9591 mL	7.3979 mL
	20 mM	0.2219 mL	1.1097 mL	2.2194 mL	5.5484 mL
	25 mM	0.1775 mL	0.8877 mL	1.7755 mL	4.4387 mL
	30 mM	0.1480 mL	0.7398 mL	1.4796 mL	3.6989 mL
	40 mM	0.1110 mL	0.5548 mL	1.1097 mL	2.7742 mL
	50 mM	0.0888 mL	0.4439 mL	0.8877 mL	2.2194 mL
	60 mM	0.0740 mL	0.3699 mL	0.7398 mL	1.8495 mL
	80 mM	0.0555 mL	0.2774 mL	0.5548 mL	1.3871 mL
	100 mM	0.0444 mL	0.2219 mL	0.4439 mL	1.1097 mL