Home - Products - Cell Cycle/DNA Damage - Potassium Channel - Methyl 4-hydroxycinnamate (b)

Methyl 4-hydroxycinnamate (b)

CAS No. 19367-38-5

Methyl 4-hydroxycinnamate (b)( pCAME | p-CAME | p CAME )

Catalog No. M18184 CAS No. 19367-38-5

Methyl trans-p-Coumarat is a predicted metabolite generated by BioTransformer1 that is produced by the metabolism of methyl 3-phenylprop-2-enoate.

Purity : >98% (HPLC)

COA

Datasheet

HNMR

HPLC

MSDS

Handing Instructions

Size	Price / USD	Stock	Quantity
100MG	38	In Stock
200MG	Get Quote	In Stock
500MG	Get Quote	In Stock
1G	Get Quote	In Stock

Get Quotation Bulk Inquiry Add to Cart

Biological Information

Product Name

Methyl 4-hydroxycinnamate (b)
Note

Research use only, not for human use.
Brief Description

Methyl trans-p-Coumarat is a predicted metabolite generated by BioTransformer1 that is produced by the metabolism of methyl 3-phenylprop-2-enoate.
Description

pCAME is an inducer of ectopic tail formation of zebrafish.
In Vitro

——
In Vivo

——
Synonyms

pCAME | p-CAME | p CAME
Pathway

Cell Cycle/DNA Damage
Target

Potassium Channel
Recptor

Others
Research Area

Others-Field
Indication

——

Chemical Information

CAS Number

19367-38-5
Formula Weight

178.18
Molecular Formula

C10H10O3
Purity

>98% (HPLC)
Solubility

In Vitro:?DMSO : 100 mg/mL (561.23 mM)
SMILES

COC(=O)/C=C/c1ccc(cc1)O
Chemical Name

3-(4-Hydroxy-phenyl)-acrylic acid methyl ester

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

1.Tan EM, et al. J Phys Chem B. 2013 May 2;117(17):4798-805.

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog

related products

AM-92016 hydrochlori...

AM-92016 is a specific blocker of rectifier potassium current. AM-92016 delays rectifier potassium channel and repolarizes the membrane thereby restricting the duration of the nerve impulse.
Nateglinide

Nateglinide is an oral antihyperglycemic agent used for the treatment of non-insulin-dependent diabetes mellitus (NIDDM).
RU-TRAAK-2

RU-TRAAK-2 is a reversible inhibitor of TWIK-related arachidonic acid-stimulated K+ channel with no activity for non-K2P channels including Kv1.2, GIRK2, and Slo1.

Sign In Join Free